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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2017-03-21 06:18:04 UTC

Update Date

2022-03-07 03:17:54 UTC

HMDB ID

HMDB0062425

Secondary Accession Numbers

HMDB62425

Metabolite Identification

Common Name

5-S-glutathionyl-L-DOPA

Description

(2S)-2-amino-4-{[(1R)-2-({5-[(2S)-2-amino-2-carboxyethyl]-2,3-dihydroxyphenyl}sulfanyl)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds (2S)-2-amino-4-{[(1R)-2-({5-[(2S)-2-amino-2-carboxyethyl]-2,3-dihydroxyphenyl}sulfanyl)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652303211707182D          

 37 37  0  0  1  0            999 V2000
    2.8579   -4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -8.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  6  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  4  0  0  0
  6  8  2  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 15 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  4  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
  2 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
M  END

HMDB0062425
     RDKit          3D
5-S-glutathionyl-L-DOPA
 60 60  0  0  0  0  0  0  0  0999 V2000
   -4.6356   -4.4989   -0.1253 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0077   -3.1202   -0.4899 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8006   -2.2770   -0.2547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9593   -0.8133   -0.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6503   -0.1827   -0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5345   -0.6165   -0.9115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5897    0.7226    0.6326 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5063    1.4841    1.1336 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2086    0.9833    0.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1342    2.0230    1.2444 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.6630    1.4171    0.5303 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3539    0.4051    1.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5321   -0.1171    0.7149 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2003   -1.1810    1.4699 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7851   -2.5694    1.0968 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5593   -3.4797    1.9557 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0634   -2.9406   -0.2931 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5018   -2.3001   -1.2179 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9203   -3.9703   -0.6773 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0158    0.4119   -0.4714 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240    1.4227   -1.1300 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8370    1.9212   -2.3050 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1566    1.9244   -0.6371 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4442    2.9356   -1.2758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6169    2.9170    0.7087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6251    3.7837    1.1266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6044    3.2622   -0.0062 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8692    4.5771   -0.5002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8305    5.3345    0.3221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3249    4.8082    1.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1521    6.6228   -0.0771 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3887   -3.0632   -1.9095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8291   -2.0125   -2.4020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2544   -4.1867   -2.6952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8810   -4.4775    0.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4647   -5.0391    0.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8287   -2.8569    0.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9111   -2.6276   -0.8454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4597   -2.3508    0.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2016   -0.6171   -1.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7300   -0.3451    0.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4268   -0.4694   -1.9089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4437    1.4170    2.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0544   -0.0677    0.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1743    1.2073   -0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9537    0.0075    2.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2984   -1.0282    1.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9452   -1.0481    2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7236   -2.6974    1.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5204   -3.0840    2.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1187   -3.4891    2.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9251   -3.9260   -0.5721 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9409    0.0108   -0.8560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4030    2.6457   -2.8387 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5795    3.2976   -0.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5735    4.1826    2.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2204    4.4782   -1.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8946    5.1168   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5351    7.2085   -0.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7119   -5.0751   -2.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 17 19  1  0
 13 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
  8 25  1  0
 25 26  1  0
 25 27  2  3
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
  2 32  1  0
 32 33  2  0
 32 34  1  0
 23 11  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  1
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  6 42  1  0
  8 43  1  1
  9 44  1  0
  9 45  1  0
 12 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  1
 16 50  1  0
 16 51  1  0
 19 52  1  0
 20 53  1  0
 22 54  1  0
 24 55  1  0
 26 56  1  0
 28 57  1  0
 28 58  1  0
 31 59  1  0
 34 60  1  0
M  END


  Mrv1652303211707182D          

 37 37  0  0  1  0            999 V2000
    2.8579   -4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -8.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  6  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  4  0  0  0
  6  8  2  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 15 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  4  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
  2 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0062425

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1=CC(C[C@]([H])(N)C(O)=O)=CC(O)=C1O)C(O)=NCC(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H26N4O10S/c20-9(18(30)31)1-2-14(25)23-11(17(29)22-6-15(26)27)7-34-13-5-8(3-10(21)19(32)33)4-12(24)16(13)28/h4-5,9-11,24,28H,1-3,6-7,20-21H2,(H,22,29)(H,23,25)(H,26,27)(H,30,31)(H,32,33)/t9-,10-,11-/m0/s1

> <INCHI_KEY>
QPUCCRKMCAEIND-DCAQKATOSA-N

> <FORMULA>
C19H26N4O10S

> <MOLECULAR_WEIGHT>
502.5

> <EXACT_MASS>
502.136964227

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
48.080193574951124

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-amino-4-{[(1R)-2-({5-[(2S)-2-amino-2-carboxyethyl]-2,3-dihydroxyphenyl}sulfanyl)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

> <ALOGPS_LOGP>
-2.99

> <JCHEM_LOGP>
-5.389293800283592

> <ALOGPS_LOGS>
-3.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
1.8701308529344685

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2671011564600443

> <JCHEM_PKA_STRONGEST_BASIC>
9.932119660197863

> <JCHEM_POLAR_SURFACE_AREA>
269.5799999999999

> <JCHEM_REFRACTIVITY>
117.75459999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.61e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-amino-4-{[(1R)-2-({5-[(2S)-2-amino-2-carboxyethyl]-2,3-dihydroxyphenyl}sulfanyl)-1-(carboxymethyl-C-hydroxycarbonimidoyl)ethyl]-C-hydroxycarbonimidoyl}butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0062425
     RDKit          3D
5-S-glutathionyl-L-DOPA
 60 60  0  0  0  0  0  0  0  0999 V2000
   -4.6356   -4.4989   -0.1253 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0077   -3.1202   -0.4899 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8006   -2.2770   -0.2547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9593   -0.8133   -0.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6503   -0.1827   -0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5345   -0.6165   -0.9115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5897    0.7226    0.6326 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5063    1.4841    1.1336 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2086    0.9833    0.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1342    2.0230    1.2444 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.6630    1.4171    0.5303 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3539    0.4051    1.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5321   -0.1171    0.7149 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2003   -1.1810    1.4699 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7851   -2.5694    1.0968 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5593   -3.4797    1.9557 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0634   -2.9406   -0.2931 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5018   -2.3001   -1.2179 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9203   -3.9703   -0.6773 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0158    0.4119   -0.4714 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240    1.4227   -1.1300 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8370    1.9212   -2.3050 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1566    1.9244   -0.6371 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4442    2.9356   -1.2758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6169    2.9170    0.7087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6251    3.7837    1.1266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6044    3.2622   -0.0062 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8692    4.5771   -0.5002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8305    5.3345    0.3221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3249    4.8082    1.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1521    6.6228   -0.0771 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3887   -3.0632   -1.9095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8291   -2.0125   -2.4020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2544   -4.1867   -2.6952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8810   -4.4775    0.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4647   -5.0391    0.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8287   -2.8569    0.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9111   -2.6276   -0.8454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4597   -2.3508    0.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2016   -0.6171   -1.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7300   -0.3451    0.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4268   -0.4694   -1.9089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4437    1.4170    2.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0544   -0.0677    0.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1743    1.2073   -0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9537    0.0075    2.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2984   -1.0282    1.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9452   -1.0481    2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7236   -2.6974    1.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5204   -3.0840    2.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1187   -3.4891    2.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9251   -3.9260   -0.5721 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9409    0.0108   -0.8560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4030    2.6457   -2.8387 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5795    3.2976   -0.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5735    4.1826    2.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2204    4.4782   -1.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8946    5.1168   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5351    7.2085   -0.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7119   -5.0751   -2.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 17 19  1  0
 13 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
  8 25  1  0
 25 26  1  0
 25 27  2  3
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
  2 32  1  0
 32 33  2  0
 32 34  1  0
 23 11  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  1
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  6 42  1  0
  8 43  1  1
  9 44  1  0
  9 45  1  0
 12 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  1
 16 50  1  0
 16 51  1  0
 19 52  1  0
 20 53  1  0
 22 54  1  0
 24 55  1  0
 26 56  1  0
 28 57  1  0
 28 58  1  0
 31 59  1  0
 34 60  1  0
M  END

HEADER    PROTEIN                                 21-MAR-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-MAR-17         0                                  
HETATM    1  H   UNK     0       5.335  -7.700   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       6.668  -8.470   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       6.668  -6.930   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667 -10.780   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       1.334  -8.470   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   10  H   UNK     0       0.000  -7.700   0.000  0.00  0.00           H+0
HETATM   11  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   12  S   UNK     0      -2.667  -9.240   0.000  0.00  0.00           S+0
HETATM   13  C   UNK     0      -4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -9.336  -8.470   0.000  0.00  0.00           C+0
HETATM   18  H   UNK     0      -8.002  -7.700   0.000  0.00  0.00           H+0
HETATM   19  N   UNK     0      -9.336  -6.930   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0     -10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0     -12.003  -8.470   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0     -10.669 -10.780   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.667  -6.160   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       0.000 -10.780   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.334 -11.550   0.000  0.00  0.00           O+0
HETATM   30  N   UNK     0       1.334 -11.550   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       1.334 -13.090   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.001 -13.090   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       2.667 -15.400   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       9.336  -8.470   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       8.002 -10.780   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   35                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11   28                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   15   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   13   27                                                  
CONECT   27   26                                                            
CONECT   28    9   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35    2   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   74    0
END

COMPND    HMDB0062425
HETATM    1  N1  UNL     1      -4.636  -4.499  -0.125  1.00  0.00           N  
HETATM    2  C1  UNL     1      -5.008  -3.120  -0.490  1.00  0.00           C  
HETATM    3  C2  UNL     1      -3.801  -2.277  -0.255  1.00  0.00           C  
HETATM    4  C3  UNL     1      -3.959  -0.813  -0.560  1.00  0.00           C  
HETATM    5  C4  UNL     1      -2.650  -0.183  -0.238  1.00  0.00           C  
HETATM    6  O1  UNL     1      -1.535  -0.617  -0.912  1.00  0.00           O  
HETATM    7  N2  UNL     1      -2.590   0.723   0.633  1.00  0.00           N  
HETATM    8  C5  UNL     1      -1.506   1.484   1.134  1.00  0.00           C  
HETATM    9  C6  UNL     1      -0.209   0.983   0.539  1.00  0.00           C  
HETATM   10  S1  UNL     1       1.134   2.023   1.244  1.00  0.00           S  
HETATM   11  C7  UNL     1       2.663   1.417   0.530  1.00  0.00           C  
HETATM   12  C8  UNL     1       3.354   0.405   1.191  1.00  0.00           C  
HETATM   13  C9  UNL     1       4.532  -0.117   0.715  1.00  0.00           C  
HETATM   14  C10 UNL     1       5.200  -1.181   1.470  1.00  0.00           C  
HETATM   15  C11 UNL     1       4.785  -2.569   1.097  1.00  0.00           C  
HETATM   16  N3  UNL     1       5.559  -3.480   1.956  1.00  0.00           N  
HETATM   17  C12 UNL     1       5.063  -2.941  -0.293  1.00  0.00           C  
HETATM   18  O2  UNL     1       4.502  -2.300  -1.218  1.00  0.00           O  
HETATM   19  O3  UNL     1       5.920  -3.970  -0.677  1.00  0.00           O  
HETATM   20  C13 UNL     1       5.016   0.412  -0.471  1.00  0.00           C  
HETATM   21  C14 UNL     1       4.324   1.423  -1.130  1.00  0.00           C  
HETATM   22  O4  UNL     1       4.837   1.921  -2.305  1.00  0.00           O  
HETATM   23  C15 UNL     1       3.157   1.924  -0.637  1.00  0.00           C  
HETATM   24  O5  UNL     1       2.444   2.936  -1.276  1.00  0.00           O  
HETATM   25  C16 UNL     1      -1.617   2.917   0.709  1.00  0.00           C  
HETATM   26  O6  UNL     1      -0.625   3.784   1.127  1.00  0.00           O  
HETATM   27  N4  UNL     1      -2.604   3.262  -0.006  1.00  0.00           N  
HETATM   28  C17 UNL     1      -2.869   4.577  -0.500  1.00  0.00           C  
HETATM   29  C18 UNL     1      -3.830   5.334   0.322  1.00  0.00           C  
HETATM   30  O7  UNL     1      -4.325   4.808   1.342  1.00  0.00           O  
HETATM   31  O8  UNL     1      -4.152   6.623  -0.077  1.00  0.00           O  
HETATM   32  C19 UNL     1      -5.389  -3.063  -1.910  1.00  0.00           C  
HETATM   33  O9  UNL     1      -5.829  -2.012  -2.402  1.00  0.00           O  
HETATM   34  O10 UNL     1      -5.254  -4.187  -2.695  1.00  0.00           O  
HETATM   35  H1  UNL     1      -3.881  -4.478   0.613  1.00  0.00           H  
HETATM   36  H2  UNL     1      -5.465  -5.039   0.199  1.00  0.00           H  
HETATM   37  H3  UNL     1      -5.829  -2.857   0.194  1.00  0.00           H  
HETATM   38  H4  UNL     1      -2.911  -2.628  -0.845  1.00  0.00           H  
HETATM   39  H5  UNL     1      -3.460  -2.351   0.813  1.00  0.00           H  
HETATM   40  H6  UNL     1      -4.202  -0.617  -1.637  1.00  0.00           H  
HETATM   41  H7  UNL     1      -4.730  -0.345   0.090  1.00  0.00           H  
HETATM   42  H8  UNL     1      -1.427  -0.469  -1.909  1.00  0.00           H  
HETATM   43  H9  UNL     1      -1.444   1.417   2.250  1.00  0.00           H  
HETATM   44  H10 UNL     1      -0.054  -0.068   0.777  1.00  0.00           H  
HETATM   45  H11 UNL     1      -0.174   1.207  -0.556  1.00  0.00           H  
HETATM   46  H12 UNL     1       2.954   0.008   2.120  1.00  0.00           H  
HETATM   47  H13 UNL     1       6.298  -1.028   1.410  1.00  0.00           H  
HETATM   48  H14 UNL     1       4.945  -1.048   2.551  1.00  0.00           H  
HETATM   49  H15 UNL     1       3.724  -2.697   1.384  1.00  0.00           H  
HETATM   50  H16 UNL     1       6.520  -3.084   2.076  1.00  0.00           H  
HETATM   51  H17 UNL     1       5.119  -3.489   2.892  1.00  0.00           H  
HETATM   52  H18 UNL     1       6.925  -3.926  -0.572  1.00  0.00           H  
HETATM   53  H19 UNL     1       5.941   0.011  -0.856  1.00  0.00           H  
HETATM   54  H20 UNL     1       4.403   2.646  -2.839  1.00  0.00           H  
HETATM   55  H21 UNL     1       1.580   3.298  -0.898  1.00  0.00           H  
HETATM   56  H22 UNL     1      -0.574   4.183   2.045  1.00  0.00           H  
HETATM   57  H23 UNL     1      -3.220   4.478  -1.564  1.00  0.00           H  
HETATM   58  H24 UNL     1      -1.895   5.117  -0.572  1.00  0.00           H  
HETATM   59  H25 UNL     1      -3.535   7.208  -0.619  1.00  0.00           H  
HETATM   60  H26 UNL     1      -5.712  -5.075  -2.500  1.00  0.00           H  
CONECT    1    2   35   36
CONECT    2    3   32   37
CONECT    3    4   38   39
CONECT    4    5   40   41
CONECT    5    6    7    7
CONECT    6   42
CONECT    7    8
CONECT    8    9   25   43
CONECT    9   10   44   45
CONECT   10   11
CONECT   11   12   12   23
CONECT   12   13   46
CONECT   13   14   20   20
CONECT   14   15   47   48
CONECT   15   16   17   49
CONECT   16   50   51
CONECT   17   18   18   19
CONECT   19   52
CONECT   20   21   53
CONECT   21   22   23   23
CONECT   22   54
CONECT   23   24
CONECT   24   55
CONECT   25   26   27   27
CONECT   26   56
CONECT   27   28
CONECT   28   29   57   58
CONECT   29   30   30   31
CONECT   31   59
CONECT   32   33   33   34
CONECT   34   60
END

HMDB0062425
     RDKit          3D
5-S-glutathionyl-L-DOPA
 60 60  0  0  0  0  0  0  0  0999 V2000
   -4.6356   -4.4989   -0.1253 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0077   -3.1202   -0.4899 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8006   -2.2770   -0.2547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9593   -0.8133   -0.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6503   -0.1827   -0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5345   -0.6165   -0.9115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5897    0.7226    0.6326 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5063    1.4841    1.1336 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2086    0.9833    0.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1342    2.0230    1.2444 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.6630    1.4171    0.5303 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3539    0.4051    1.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5321   -0.1171    0.7149 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2003   -1.1810    1.4699 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7851   -2.5694    1.0968 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5593   -3.4797    1.9557 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0634   -2.9406   -0.2931 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5018   -2.3001   -1.2179 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9203   -3.9703   -0.6773 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0158    0.4119   -0.4714 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240    1.4227   -1.1300 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8370    1.9212   -2.3050 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1566    1.9244   -0.6371 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4442    2.9356   -1.2758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6169    2.9170    0.7087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6251    3.7837    1.1266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6044    3.2622   -0.0062 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8692    4.5771   -0.5002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8305    5.3345    0.3221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3249    4.8082    1.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1521    6.6228   -0.0771 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3887   -3.0632   -1.9095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8291   -2.0125   -2.4020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2544   -4.1867   -2.6952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8810   -4.4775    0.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4647   -5.0391    0.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8287   -2.8569    0.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9111   -2.6276   -0.8454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4597   -2.3508    0.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2016   -0.6171   -1.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7300   -0.3451    0.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4268   -0.4694   -1.9089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4437    1.4170    2.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0544   -0.0677    0.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1743    1.2073   -0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9537    0.0075    2.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2984   -1.0282    1.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9452   -1.0481    2.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7236   -2.6974    1.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5204   -3.0840    2.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1187   -3.4891    2.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9251   -3.9260   -0.5721 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9409    0.0108   -0.8560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4030    2.6457   -2.8387 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5795    3.2976   -0.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5735    4.1826    2.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2204    4.4782   -1.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8946    5.1168   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5351    7.2085   -0.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7119   -5.0751   -2.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 17 19  1  0
 13 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
  8 25  1  0
 25 26  1  0
 25 27  2  3
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
  2 32  1  0
 32 33  2  0
 32 34  1  0
 23 11  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  1
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  6 42  1  0
  8 43  1  1
  9 44  1  0
  9 45  1  0
 12 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  1
 16 50  1  0
 16 51  1  0
 19 52  1  0
 20 53  1  0
 22 54  1  0
 24 55  1  0
 26 56  1  0
 28 57  1  0
 28 58  1  0
 31 59  1  0
 34 60  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(2S)-2-Amino-4-{[(1R)-2-({5-[(2S)-2-amino-2-carboxyethyl]-2,3-dihydroxyphenyl}sulfanyl)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]-C-hydroxycarbonimidoyl}butanoate	Generator
(2S)-2-Amino-4-{[(1R)-2-({5-[(2S)-2-amino-2-carboxyethyl]-2,3-dihydroxyphenyl}sulphanyl)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]-C-hydroxycarbonimidoyl}butanoate	Generator
(2S)-2-Amino-4-{[(1R)-2-({5-[(2S)-2-amino-2-carboxyethyl]-2,3-dihydroxyphenyl}sulphanyl)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid	Generator

Chemical Formula

C₁₉H₂₆N₄O₁₀S

Average Molecular Weight

502.5

Monoisotopic Molecular Weight

502.136964227

IUPAC Name

(2S)-2-amino-4-{[(1R)-2-({5-[(2S)-2-amino-2-carboxyethyl]-2,3-dihydroxyphenyl}sulfanyl)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

Traditional Name

(2S)-2-amino-4-{[(1R)-2-({5-[(2S)-2-amino-2-carboxyethyl]-2,3-dihydroxyphenyl}sulfanyl)-1-(carboxymethyl-C-hydroxycarbonimidoyl)ethyl]-C-hydroxycarbonimidoyl}butanoic acid

CAS Registry Number

Not Available

SMILES

[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1=CC(C[C@]([H])(N)C(O)=O)=CC(O)=C1O)C(O)=NCC(O)=O)C(O)=O

InChI Identifier

InChI=1S/C19H26N4O10S/c20-9(18(30)31)1-2-14(25)23-11(17(29)22-6-15(26)27)7-34-13-5-8(3-10(21)19(32)33)4-12(24)16(13)28/h4-5,9-11,24,28H,1-3,6-7,20-21H2,(H,22,29)(H,23,25)(H,26,27)(H,30,31)(H,32,33)/t9-,10-,11-/m0/s1

InChI Key

QPUCCRKMCAEIND-DCAQKATOSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Gamma-glutamyl alpha peptide
Tyrosine or derivatives
Phenylalanine or derivatives
Glutamine or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
Alpha-amino acid amide
Cysteine or derivatives
3-phenylpropanoic-acid
Alpha-amino acid
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Amphetamine or derivatives
L-alpha-amino acid
Tricarboxylic acid or derivatives
Aryl thioether
Catechol
Thiophenol ether
Aralkylamine
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Phenol
Alkylarylthioether
N-acyl-amine
Fatty amide
Fatty acyl
Monocyclic benzene moiety
Benzenoid
Amino acid
Amino acid or derivatives
Carboxamide group
Secondary carboxylic acid amide
Thioether
Carboxylic acid
Sulfenyl compound
Primary amine
Organic nitrogen compound
Organic oxide
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Amine
Primary aliphatic amine
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	0.36 g/l	ALOGPS
LogP	-3.39	ALOGPS

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-3	ALOGPS
logP	-5.4	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	1.27	ChemAxon
pKa (Strongest Basic)	9.93	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	269.58 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	117.75 m³·mol⁻¹	ChemAxon
Polarizability	48.08 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	213.418	31661259
DarkChem	[M-H]-	204.22	31661259
DeepCCS	[M+H]+	204.721	30932474
DeepCCS	[M-H]-	202.826	30932474
DeepCCS	[M-2H]-	236.068	30932474
DeepCCS	[M+Na]+	210.5	30932474
AllCCS	[M+H]+	207.2	32859911
AllCCS	[M+H-H2O]+	205.7	32859911
AllCCS	[M+NH4]+	208.5	32859911
AllCCS	[M+Na]+	208.9	32859911
AllCCS	[M-H]-	204.4	32859911
AllCCS	[M+Na-2H]-	205.6	32859911
AllCCS	[M+HCOO]-	207.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
5-S-glutathionyl-L-DOPA	[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1=CC(C[C@]([H])(N)C(O)=O)=CC(O)=C1O)C(O)=NCC(O)=O)C(O)=O	5253.2	Standard polar	33892256
5-S-glutathionyl-L-DOPA	[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1=CC(C[C@]([H])(N)C(O)=O)=CC(O)=C1O)C(O)=NCC(O)=O)C(O)=O	4083.2	Standard non polar	33892256
5-S-glutathionyl-L-DOPA	[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1=CC(C[C@]([H])(N)C(O)=O)=CC(O)=C1O)C(O)=NCC(O)=O)C(O)=O	4703.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
5-S-glutathionyl-L-DOPA,1TMS,isomer #1	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O	4499.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TMS,isomer #2	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1	4466.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TMS,isomer #3	C[Si](C)(C)OC1=CC(C[C@H](N)C(=O)O)=CC(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1O	4502.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TMS,isomer #4	C[Si](C)(C)OC1=C(O)C=C(C[C@H](N)C(=O)O)C=C1SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O	4418.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TMS,isomer #5	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4445.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TMS,isomer #6	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4482.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TMS,isomer #7	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O	4447.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TMS,isomer #8	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4597.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TMS,isomer #9	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O	4595.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #1	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C	4293.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #10	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1	4251.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #11	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O	4255.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #12	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4267.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #13	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4287.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #14	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4407.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #15	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4405.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #16	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O	4290.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #17	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4294.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #18	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4328.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #19	C[Si](C)(C)OC1=CC(C[C@H](N)C(=O)O)=CC(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1O[Si](C)(C)C	4312.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #2	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4318.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #20	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O	4448.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #21	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O	4441.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #22	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4231.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #23	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4250.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #24	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4267.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #25	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O	4365.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #26	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4364.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #27	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4270.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #28	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4247.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #29	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4425.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #3	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O	4357.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #30	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4424.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #31	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4266.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #32	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4426.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #33	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4419.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #34	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4398.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #35	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4394.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #36	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4546.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #37	C[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C	4591.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #38	C[Si](C)(C)N([C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O)[Si](C)(C)C	4629.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #4	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4296.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #5	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4314.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #6	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4341.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #7	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4455.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #8	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4460.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TMS,isomer #9	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1	4307.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #1	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C	4143.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #10	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4146.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #100	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4575.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #11	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4168.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #12	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4280.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #13	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4294.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #14	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4220.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #15	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4173.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #16	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4206.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #17	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4320.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #18	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4326.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #19	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C	4175.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #2	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C	4172.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #20	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4175.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #21	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4285.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #22	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4294.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #23	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4149.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #24	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4293.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #25	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4298.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #26	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4305.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #27	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4305.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #28	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4436.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #29	C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O	4460.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #3	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C	4153.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #30	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O	4483.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #31	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1	4190.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #32	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O	4153.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #33	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4130.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #34	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4187.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #35	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4271.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #36	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O	4280.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #37	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4125.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #38	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4119.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #39	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4147.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #4	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	4137.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #40	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4224.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #41	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4235.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #42	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4084.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #43	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4123.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #44	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4230.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #45	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4224.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #46	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4099.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #47	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4236.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #48	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4246.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #49	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4253.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #5	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	4159.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #50	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4261.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #51	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4380.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #52	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4458.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #53	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4427.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #54	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4172.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #55	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4117.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #56	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4176.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #57	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4260.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #58	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4273.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #59	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4137.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #6	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4280.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #60	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4173.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #61	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4281.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #62	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4275.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #63	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4202.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #64	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4304.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #65	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4298.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #66	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O	4331.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #67	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4320.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #68	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O	4425.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #69	C[Si](C)(C)OC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1O	4482.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #7	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4281.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #70	C[Si](C)(C)OC1=CC(C[C@H](N)C(=O)O)=CC(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1O	4442.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #71	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C	4108.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #72	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4133.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #73	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4213.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #74	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4230.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #75	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4116.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #76	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4256.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #77	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4251.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #78	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4256.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #79	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4247.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #8	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4188.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #80	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4364.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #81	C[Si](C)(C)OC1=C(O)C=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O	4429.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #82	C[Si](C)(C)OC1=C(O)C=C(C[C@H](N)C(=O)O)C=C1SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O	4399.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #83	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4091.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #84	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4244.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #85	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4245.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #86	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4232.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #87	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4235.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #88	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4403.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #89	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4449.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #9	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4172.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #90	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4418.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #91	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4252.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #92	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4247.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #93	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4399.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #94	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4469.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #95	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4442.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #96	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4378.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #97	C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4427.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #98	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O	4444.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TMS,isomer #99	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4545.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #1	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C	4086.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #10	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4201.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #100	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	3996.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #101	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4137.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #102	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4121.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #103	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4145.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #104	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4158.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #105	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4254.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #106	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4302.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #107	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O	4306.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #108	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4129.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #109	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4149.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #11	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4205.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #110	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4266.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #111	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	4306.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #112	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4298.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #113	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4272.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #114	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4321.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #115	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4307.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #116	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4407.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #117	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4445.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #118	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C	4102.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #119	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4120.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #12	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	4093.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #120	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4211.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #121	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4232.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #122	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4039.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #123	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4162.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #124	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4164.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #125	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4204.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #126	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4194.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #127	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4298.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #128	C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4316.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #129	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O	4333.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #13	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	4084.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #130	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4101.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #131	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4166.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #132	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4181.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #133	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4236.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #134	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4239.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #135	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4301.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #136	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4323.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #137	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4298.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #138	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4242.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #139	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4238.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #14	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4183.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #140	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4321.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #141	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4357.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #142	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4331.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #143	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4365.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #144	C[Si](C)(C)OC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1O[Si](C)(C)C	4397.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #145	C[Si](C)(C)OC1=CC(C[C@H](N)C(=O)O)=CC(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1O[Si](C)(C)C	4365.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #146	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4437.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #147	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O	4457.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #148	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4054.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #149	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4155.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #15	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4193.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #150	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4161.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #151	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4170.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #152	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4156.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #153	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4257.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #154	C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4285.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #155	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4313.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #156	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4157.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #157	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4167.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #158	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4291.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #159	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4318.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #16	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	4026.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #160	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4297.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #161	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4284.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #162	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4330.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #163	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4308.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #164	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4420.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #165	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4438.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #166	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4126.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #167	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4140.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #168	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4268.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #169	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4314.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #17	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4173.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #170	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4294.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #171	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4262.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #172	C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4292.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #173	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4315.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #174	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4416.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #175	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4438.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #176	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4274.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #177	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4322.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #178	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4307.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #179	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4427.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #18	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4172.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #180	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4452.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #181	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4438.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #182	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4429.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #183	C[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C	4624.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #19	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4182.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #2	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C	4079.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #20	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4189.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #21	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4308.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #22	C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4344.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #23	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C	4348.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #24	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4136.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #25	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4076.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #26	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4102.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #27	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4202.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #28	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4223.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #29	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4096.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #3	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	4034.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #30	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4086.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #31	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4179.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #32	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4207.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #33	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4023.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #34	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4163.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #35	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4190.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #36	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4181.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #37	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4201.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #38	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4307.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #39	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4350.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #4	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	4048.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #40	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4345.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #41	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C	4137.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #42	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4133.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #43	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4272.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #44	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4274.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #45	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4068.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #46	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4215.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #47	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4210.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #48	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4222.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #49	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4229.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #5	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4175.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #50	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4347.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #51	C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O	4348.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #52	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O	4366.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #53	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4089.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #54	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4223.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #55	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4220.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #56	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4201.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #57	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4206.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #58	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4328.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #59	C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4350.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #6	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4161.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #60	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4365.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #61	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4174.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #62	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4187.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #63	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4307.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #64	C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4336.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #65	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4351.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #66	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4325.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #67	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4360.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #68	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	4346.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #69	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4464.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #7	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C	4123.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #70	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4472.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #71	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4119.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #72	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4110.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #73	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4125.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #74	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4221.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #75	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4242.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #76	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4042.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #77	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4084.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #78	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4184.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #79	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4176.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #8	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	4064.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #80	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4051.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #81	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4158.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #82	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4185.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #83	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4198.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #84	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4216.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #85	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O	4301.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #86	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4336.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #87	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4320.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #88	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C	4057.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #89	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4071.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #9	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	4089.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #90	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4158.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #91	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4147.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #92	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4056.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #93	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4149.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #94	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4175.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #95	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4156.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #96	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4180.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #97	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4257.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #98	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4303.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,4TMS,isomer #99	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4303.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #1	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C	4049.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #10	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	3923.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #100	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C	4299.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #101	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4263.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #102	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4280.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #103	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	4277.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #104	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4382.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #105	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4393.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #106	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4232.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #107	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4264.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #108	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	4269.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #109	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4373.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #11	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4075.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #110	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4389.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #111	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4370.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #112	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4380.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #113	C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O	4553.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #114	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C	4036.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #115	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4046.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #116	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4160.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #117	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4149.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #118	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4039.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #119	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4152.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #12	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4061.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #120	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4192.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #121	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4165.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #122	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4185.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #123	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4279.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #124	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4305.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #125	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4310.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #126	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	3951.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #127	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4078.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #128	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4068.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #129	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4103.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #13	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4068.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #130	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4106.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #131	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4205.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #132	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4253.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #133	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O	4242.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #134	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4080.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #135	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4094.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #136	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4210.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #137	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	4217.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #138	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4230.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #139	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4234.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #14	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4079.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #140	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4252.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #141	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4251.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #142	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4329.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #143	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O	4354.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #144	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	3975.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #145	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4101.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #146	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4081.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #147	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4089.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #148	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4100.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #149	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4184.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #15	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4194.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #150	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4244.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #151	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4234.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #152	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4087.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #153	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4114.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #154	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4215.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #155	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	4227.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #156	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4249.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #157	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4206.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #158	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4237.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #159	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4248.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #16	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4254.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #160	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4321.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #161	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4343.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #162	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4020.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #163	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4034.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #164	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4159.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #165	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4210.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #166	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4206.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #167	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4180.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #168	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4213.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #169	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4220.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #17	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C	4242.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #170	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4321.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #171	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4332.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #172	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4171.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #173	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4203.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #174	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4203.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #175	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4314.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #176	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4337.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #177	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4326.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #178	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4343.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #179	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4547.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #18	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	4062.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #180	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4028.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #181	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4156.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #182	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4167.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #183	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4170.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #184	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4160.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #185	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4280.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #186	C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4293.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #187	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4314.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #188	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4082.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #189	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4081.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #19	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	4062.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #190	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4210.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #191	C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4218.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #192	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4233.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #193	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4233.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #194	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4248.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #195	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4253.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #196	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4340.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #197	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4343.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #198	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4159.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #199	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4174.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #2	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	3989.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #20	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4179.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #200	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4219.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #201	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4227.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #202	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4225.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #203	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4305.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #204	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4309.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #205	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4292.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #206	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4320.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #207	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4344.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #208	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4302.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #209	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4320.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #21	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4190.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #210	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4305.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #211	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4339.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #212	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4354.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #213	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4407.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #214	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O	4427.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #215	C[Si](C)(C)OC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1O	4515.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #216	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4098.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #217	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4096.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #218	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4218.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #219	C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4228.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #22	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	3982.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #220	C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C	4253.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #221	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4208.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #222	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4244.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #223	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4238.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #224	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C	4336.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #225	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4336.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #226	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4226.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #227	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4237.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #228	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4235.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #229	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4340.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #23	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4110.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #230	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4360.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #231	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4337.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #232	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O	4351.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #233	C[Si](C)(C)OC1=C(O)C=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O	4518.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #234	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4171.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #235	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C	4205.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #236	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4207.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #237	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4312.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #238	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4338.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #239	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4335.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #24	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4124.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #240	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4320.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #241	C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4516.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #242	C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4339.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #243	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4331.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #244	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4533.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #245	C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C	4554.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #25	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4118.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #26	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4121.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #27	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4244.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #28	C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4264.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #29	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C	4267.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #3	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	3993.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #30	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	4010.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #31	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4137.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #32	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4148.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #33	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4119.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #34	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4117.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #35	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4239.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #36	C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4264.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #37	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C	4280.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #38	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4074.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #39	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4066.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #4	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4107.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #40	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4222.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #41	C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	4260.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #42	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	4268.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #43	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4219.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #44	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	4251.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #45	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	4260.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #46	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4369.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #47	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4374.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #48	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4074.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #49	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4069.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #5	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4099.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #50	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4175.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #51	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4211.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #52	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	3988.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #53	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4106.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #54	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4138.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #55	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4123.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #56	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4130.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #57	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4244.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #58	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4262.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #59	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4274.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #6	C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	4018.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #60	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4016.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #61	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4127.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #62	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4167.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #63	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4114.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #64	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4134.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #65	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4235.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #66	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)N([Si](C)(C)C)[Si](C)(C)C	4262.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #67	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1	4285.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #68	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C	4060.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #69	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4086.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #7	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C	4002.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #70	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4219.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #71	C[Si](C)(C)OC(=O)[C@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C	4253.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #72	C[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1	4269.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #73	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4216.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #74	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4250.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #75	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	4258.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #76	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4356.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #77	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4379.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #78	C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4066.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #79	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4223.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #8	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4114.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #80	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)=C1)C(=O)O	4213.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #81	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)=C1)C(=O)O	4196.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #82	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4204.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #83	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4335.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #84	C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4334.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #85	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C)C(O)=NCC(=O)O	4346.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #86	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4116.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #87	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4126.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #88	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4266.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #89	C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4269.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #9	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C	4096.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #90	C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C	4274.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #91	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4267.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #92	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C	4271.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #93	C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1O)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	4270.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #94	C[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4366.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #95	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O	4376.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #96	C[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)=C1)C(=O)O	4141.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #97	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4151.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #98	C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	4287.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,5TMS,isomer #99	C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C	4289.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O	4699.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1	4695.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(C[C@H](N)C(=O)O)=CC(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1O	4687.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C[C@H](N)C(=O)O)C=C1SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O	4642.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4646.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4724.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O	4675.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4774.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O	4777.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4708.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1	4694.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O	4699.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1	4676.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4747.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	4802.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4784.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O	4700.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4674.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4771.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC(C[C@H](N)C(=O)O)=CC(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1O[Si](C)(C)C(C)(C)C	4700.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1	4722.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O	4795.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O	4795.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O	4676.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4662.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4743.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O	4756.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)C(=O)O	4752.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4703.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4666.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4774.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O	4738.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4769.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C	4735.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4826.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4822.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	4793.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4773.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4876.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	4921.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)N([C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O)[Si](C)(C)C(C)(C)C	4938.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O	4728.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4697.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C	4773.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4815.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4820.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1	4712.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4781.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1	4768.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #100	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	5090.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C	4828.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	4876.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4873.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O	4848.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4808.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C	4871.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4922.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4908.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4804.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4812.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C	4862.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4908.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4903.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C	4798.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4868.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4866.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4911.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4924.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4973.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O	5042.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4806.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O	5046.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1	4800.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O	4788.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1	4757.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4833.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	4863.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O	4859.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O	4783.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1	4753.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4821.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4763.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	4841.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)C(=O)O	4842.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4731.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C	4796.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	4839.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O[Si](C)(C)C(C)(C)C	4834.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	4750.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	4827.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4819.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C	4877.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4828.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4869.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O)C(=O)O	4932.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5051.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #53	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1	5015.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #54	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O	4795.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4759.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #56	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C	4838.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #57	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	4867.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #58	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4851.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #59	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)N=C(O)CC[C@H](N)C(=O)O	4790.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4882.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #60	CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4783.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #61	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4845.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #62	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4859.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #63	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4849.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #64	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4908.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #65	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4917.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #66	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1)C(=O)O	4883.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #67	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)C(=O)O	4888.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #68	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1O)C(O)=NCC(=O)O)C(=O)O	4962.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #69	CC(C)(C)[Si](C)(C)OC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O)=C1O	5056.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4863.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #70	CC(C)(C)[Si](C)(C)OC1=CC(C[C@H](N)C(=O)O)=CC(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1O	5050.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #71	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C	4748.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #72	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C	4817.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #73	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	4845.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #74	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4836.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #75	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O	4777.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #76	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4830.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #77	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4838.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #78	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4892.2	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #79	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4894.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1	4816.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #80	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)C(=O)O	4929.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #81	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O	5030.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #82	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C[C@H](N)C(=O)O)C=C1SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O	5029.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #83	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C	4752.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #84	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4843.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #85	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4851.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #86	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4832.1	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #87	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4812.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #88	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	4927.7	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #89	CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	5010.4	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(SC[C@H](N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1	4817.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #90	CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5003.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #91	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)=C1)C(=O)O	4865.3	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #92	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4884.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #93	CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4955.8	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #94	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1O)N=C(O)CC[C@H](N)C(=O)O	5063.0	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #95	CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5054.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #96	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	4932.6	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #97	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1=CC(C[C@H](N)C(=O)O)=CC(O)=C1O)C(O)=NCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5040.5	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #98	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1=CC(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1O)C(O)=NCC(=O)O	5013.9	Semi standard non polar	33892256
5-S-glutathionyl-L-DOPA,3TBDMS,isomer #99	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CC(O)=C(O)C(SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)=C1)C(=O)O	5073.2	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS (Non-derivatized) - 70eV, Positive	splash10-06wc-3000900000-490c6e535b33024dc049	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS (2 TMS) - 70eV, Positive	splash10-0089-9401344000-1dfb4216ce1a686daf07	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS (TBDMS_2_6) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS (TBDMS_3_5) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS (TBDMS_3_11) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS (TBDMS_3_16) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS (TBDMS_3_20) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS (TBDMS_3_23) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS (TBDMS_3_27) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 5-S-glutathionyl-L-DOPA GC-MS ("5-S-glutathionyl-L-DOPA,2TBDMS,#6" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 10V, Positive-QTOF	splash10-059i-2012900000-1e16f69a4e1dc9884708	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 20V, Positive-QTOF	splash10-00di-8124900000-e1804f80866b0b2f3d48	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 40V, Positive-QTOF	splash10-00di-9321100000-6f2133e2c0156631eb98	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 10V, Negative-QTOF	splash10-0kcr-0161940000-2b6b58a7ad319f0b2ad4	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 20V, Negative-QTOF	splash10-004i-1390200000-41555e4971aa7163a716	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 40V, Negative-QTOF	splash10-00bd-2930000000-d6a5a4f293855cdbe290	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 10V, Negative-QTOF	splash10-0ul0-3254980000-01f958a989e36a4ce7c7	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 20V, Negative-QTOF	splash10-004l-2920200000-950b653a0f4c1376c690	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 40V, Negative-QTOF	splash10-006x-6900000000-8db7c1433d7be735dfa6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 10V, Positive-QTOF	splash10-0fk9-0129840000-124a02068d8512da7616	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 20V, Positive-QTOF	splash10-0pb9-1329200000-18670ce0a1f6e651454f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 5-S-glutathionyl-L-DOPA 40V, Positive-QTOF	splash10-000i-9111000000-cbf5a2a5e5868e0d7f40	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10791573

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for 5-S-glutathionyl-L-DOPA (HMDB0062425)

MOL for HMDB0062425 (5-S-glutathionyl-L-DOPA)

3D MOL for HMDB0062425 (5-S-glutathionyl-L-DOPA)

3D SDF for HMDB0062425 (5-S-glutathionyl-L-DOPA)

3D-SDF for HMDB0062425 (5-S-glutathionyl-L-DOPA)

PDB for HMDB0062425 (5-S-glutathionyl-L-DOPA)

3D PDB for HMDB0062425 (5-S-glutathionyl-L-DOPA)

SMILES for HMDB0062425 (5-S-glutathionyl-L-DOPA)

INCHI for HMDB0062425 (5-S-glutathionyl-L-DOPA)

Structure for HMDB0062425 (5-S-glutathionyl-L-DOPA)

3D Structure for HMDB0062425 (5-S-glutathionyl-L-DOPA)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra