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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2009-04-06 16:22:38 UTC

Update Date

2021-09-14 15:38:59 UTC

HMDB ID

HMDB0012303

Secondary Accession Numbers

HMDB12303

Metabolite Identification

Common Name

UDP-L-arabinose

Description

UDP-sugars, activated forms of monosaccharides, are synthesized through de novo and salvage pathways and serve as substrates for the synthesis of polysaccharides, glycolipids, and glycoproteins in higher plants. The enzyme catalyzed the formation of UDP-Glc, UDP-Gal, UDP-glucuronic acid, UDP-l-arabinose, and UDP-xylose from respective monosaccharide 1-phosphates in the presence of UTP as a co-substrate, indicating that the enzyme has broad substrate specificity toward monosaccharide 1-phosphates.

Structure

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

  Mrv1652306222023392D          

 42 44  0  0  1  0            999 V2000
   -2.4757    3.8205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9908    4.4879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2893    9.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0231    6.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4608   10.6442    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7615    6.6937    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2962    3.9067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8477   11.1962    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    7.1786    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0964    6.6937    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0631   10.9413    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8414    5.9090    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8916   10.1343    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1468    5.3278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6318    4.6604    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3264    5.2416    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2454   10.8991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7811    3.2393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0192   12.0032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    8.0036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8810    6.9486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4500   11.4933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4824    6.0815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7243    8.7951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2342    7.2259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1284    9.2439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7424    8.9009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5047    9.5823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1946    7.7556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164    5.9090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1069    9.8794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7639    8.2654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9793    8.0105    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    1.9354    9.0724    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    4.6323   11.4512    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6324    7.5085    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6762   10.3893    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1640    7.5531    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6797    6.1103    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2346   11.7483    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4669    5.1739    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2785   10.6864    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  1  0  0  0
  7  1  1  0  0  0  0
  8  5  1  0  0  0  0
  9  6  1  0  0  0  0
 10  9  1  0  0  0  0
 11  8  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 15  7  2  0  0  0  0
 15 14  1  0  0  0  0
 16  2  1  0  0  0  0
 12 16  1  1  0  0  0
 16 14  1  0  0  0  0
  5 17  1  1  0  0  0
 18  7  1  0  0  0  0
  8 19  1  6  0  0  0
  9 20  1  6  0  0  0
 10 21  1  6  0  0  0
 11 22  1  6  0  0  0
 23 14  2  0  0  0  0
 28  3  1  0  0  0  0
 28 13  1  0  0  0  0
 29  4  1  0  0  0  0
 30  6  1  0  0  0  0
 30 12  1  0  0  0  0
 13 31  1  6  0  0  0
 33 24  1  0  0  0  0
 33 25  2  0  0  0  0
 33 29  1  0  0  0  0
 33 32  1  0  0  0  0
 34 26  1  0  0  0  0
 34 27  2  0  0  0  0
 34 31  1  0  0  0  0
 34 32  1  0  0  0  0
  5 35  1  6  0  0  0
  6 36  1  6  0  0  0
  8 37  1  6  0  0  0
  9 38  1  1  0  0  0
 10 39  1  1  0  0  0
 11 40  1  1  0  0  0
 12 41  1  6  0  0  0
 13 42  1  1  0  0  0
M  END

HMDB0012303
     RDKit          3D
UDP-L-arabinose
 56 58  0  0  0  0  0  0  0  0999 V2000
   -9.0882    2.7129    0.6892 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0080    2.0862    0.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0252    0.9018   -0.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7782    0.3008   -0.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6631    0.9583   -0.3962 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4348    0.2128   -0.3549 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7799   -0.2694   -1.4028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7977   -0.9778   -0.7178 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5962   -1.4774   -1.4067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9184   -2.1589   -0.2981 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5280   -1.4196   -0.1020 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.8003   -0.4356   -1.2360 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3573   -0.3634    1.3073 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8721   -2.3289    0.2655 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1799   -1.3345   -0.2851 P   0  0  0  0  0  5  0  0  0  0  0  0
    2.8141    0.0618    0.1592 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0811   -1.4690   -1.9920 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6734   -1.8048    0.2712 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3947   -0.6377    0.5461 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5723   -0.9115    1.1357 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4260    0.1330    1.3287 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8953    1.4548    0.8323 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0105    2.0342    1.7474 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2927    1.3480   -0.5563 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3160    2.3212   -0.6352 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7096    0.0041   -0.8452 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5783   -0.8267   -1.5032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5360   -1.9029    0.1634 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8754   -2.1060    1.3600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8126   -1.1192    0.3726 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1054   -0.8182    1.6608 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6246    2.1874    0.1903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5591    2.7759    0.3833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8756    2.7198    0.5504 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9548    0.3741   -0.5129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8218   -0.6058   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7411    0.6732    0.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3730   -0.1288   -0.0055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9425   -0.7610   -1.8090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8924   -2.2943   -2.1301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365    0.5384    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8621   -2.4294   -2.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7601    0.0433    1.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4648   -0.0068    0.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5226    0.2467    2.4502 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7540    2.1448    0.7382 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2272    2.4240    1.3296 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0434    1.5953   -1.3577 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3864    2.0373   -0.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7629    0.0762   -1.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0567   -1.5320   -1.9811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7273   -2.8691   -0.3703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5572   -1.2453    1.7103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6253   -1.6406   -0.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4882   -0.1626    2.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8760    3.6710    0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  8 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  5 32  1  0
 32 33  2  0
 32 34  1  0
 34  2  1  0
 30  6  1  0
 26 19  1  0
  3 35  1  0
  4 36  1  0
  6 37  1  1
  8 38  1  1
  9 39  1  0
  9 40  1  0
 13 41  1  0
 17 42  1  0
 19 43  1  1
 21 44  1  0
 21 45  1  0
 22 46  1  6
 23 47  1  0
 24 48  1  6
 25 49  1  0
 26 50  1  6
 27 51  1  0
 28 52  1  6
 29 53  1  0
 30 54  1  6
 31 55  1  0
 34 56  1  0
M  END

  Mrv1652306222023392D          

 42 44  0  0  1  0            999 V2000
   -2.4757    3.8205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9908    4.4879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2893    9.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0231    6.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4608   10.6442    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7615    6.6937    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2962    3.9067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8477   11.1962    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    7.1786    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0964    6.6937    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0631   10.9413    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8414    5.9090    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8916   10.1343    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1468    5.3278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6318    4.6604    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3264    5.2416    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2454   10.8991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7811    3.2393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0192   12.0032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    8.0036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8810    6.9486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4500   11.4933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4824    6.0815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7243    8.7951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2342    7.2259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1284    9.2439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7424    8.9009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5047    9.5823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1946    7.7556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164    5.9090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1069    9.8794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7639    8.2654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9793    8.0105    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    1.9354    9.0724    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    4.6323   11.4512    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6324    7.5085    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6762   10.3893    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1640    7.5531    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6797    6.1103    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2346   11.7483    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4669    5.1739    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2785   10.6864    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  1  0  0  0
  7  1  1  0  0  0  0
  8  5  1  0  0  0  0
  9  6  1  0  0  0  0
 10  9  1  0  0  0  0
 11  8  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 15  7  2  0  0  0  0
 15 14  1  0  0  0  0
 16  2  1  0  0  0  0
 12 16  1  1  0  0  0
 16 14  1  0  0  0  0
  5 17  1  1  0  0  0
 18  7  1  0  0  0  0
  8 19  1  6  0  0  0
  9 20  1  6  0  0  0
 10 21  1  6  0  0  0
 11 22  1  6  0  0  0
 23 14  2  0  0  0  0
 28  3  1  0  0  0  0
 28 13  1  0  0  0  0
 29  4  1  0  0  0  0
 30  6  1  0  0  0  0
 30 12  1  0  0  0  0
 13 31  1  6  0  0  0
 33 24  1  0  0  0  0
 33 25  2  0  0  0  0
 33 29  1  0  0  0  0
 33 32  1  0  0  0  0
 34 26  1  0  0  0  0
 34 27  2  0  0  0  0
 34 31  1  0  0  0  0
 34 32  1  0  0  0  0
  5 35  1  6  0  0  0
  6 36  1  6  0  0  0
  8 37  1  6  0  0  0
  9 38  1  1  0  0  0
 10 39  1  1  0  0  0
 11 40  1  1  0  0  0
 12 41  1  6  0  0  0
 13 42  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0012303

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@]1(COP(O)(=O)OP(O)(=O)O[C@@]2([H])OC[C@]([H])(O)[C@]([H])(O)[C@@]2([H])O)O[C@@]([H])(N2C=CC(O)=NC2=O)[C@]([H])(O)[C@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C14H22N2O16P2/c17-5-3-28-13(11(22)8(5)19)31-34(26,27)32-33(24,25)29-4-6-9(20)10(21)12(30-6)16-2-1-7(18)15-14(16)23/h1-2,5-6,8-13,17,19-22H,3-4H2,(H,24,25)(H,26,27)(H,15,18,23)/t5-,6+,8-,9+,10+,11+,12+,13+/m0/s1

> <INCHI_KEY>
DQQDLYVHOTZLOR-IAZOVDBXSA-N

> <FORMULA>
C14H22N2O16P2

> <MOLECULAR_WEIGHT>
536.2758

> <EXACT_MASS>
536.04445569

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
43.613246810783565

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-hydroxy-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}({[hydroxy({[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy})phosphoryl]oxy})phosphinic acid

> <ALOGPS_LOGP>
-1.19

> <JCHEM_LOGP>
-3.9987723323333335

> <ALOGPS_LOGS>
-1.39

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.1763411018919383

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7326517523572988

> <JCHEM_PKA_STRONGEST_BASIC>
-3.526611516883185

> <JCHEM_POLAR_SURFACE_AREA>
274.8

> <JCHEM_REFRACTIVITY>
100.81499999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.18e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-hydroxy-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy([hydroxy([(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy)phosphoryl]oxy)phosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0012303
     RDKit          3D
UDP-L-arabinose
 56 58  0  0  0  0  0  0  0  0999 V2000
   -9.0882    2.7129    0.6892 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0080    2.0862    0.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0252    0.9018   -0.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7782    0.3008   -0.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6631    0.9583   -0.3962 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4348    0.2128   -0.3549 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7799   -0.2694   -1.4028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7977   -0.9778   -0.7178 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5962   -1.4774   -1.4067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9184   -2.1589   -0.2981 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5280   -1.4196   -0.1020 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.8003   -0.4356   -1.2360 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3573   -0.3634    1.3073 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8721   -2.3289    0.2655 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1799   -1.3345   -0.2851 P   0  0  0  0  0  5  0  0  0  0  0  0
    2.8141    0.0618    0.1592 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0811   -1.4690   -1.9920 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6734   -1.8048    0.2712 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3947   -0.6377    0.5461 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5723   -0.9115    1.1357 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4260    0.1330    1.3287 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8953    1.4548    0.8323 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0105    2.0342    1.7474 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2927    1.3480   -0.5563 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3160    2.3212   -0.6352 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7096    0.0041   -0.8452 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5783   -0.8267   -1.5032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5360   -1.9029    0.1634 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8754   -2.1060    1.3600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8126   -1.1192    0.3726 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1054   -0.8182    1.6608 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6246    2.1874    0.1903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5591    2.7759    0.3833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8756    2.7198    0.5504 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9548    0.3741   -0.5129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8218   -0.6058   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7411    0.6732    0.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3730   -0.1288   -0.0055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9425   -0.7610   -1.8090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8924   -2.2943   -2.1301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365    0.5384    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8621   -2.4294   -2.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7601    0.0433    1.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4648   -0.0068    0.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5226    0.2467    2.4502 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7540    2.1448    0.7382 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2272    2.4240    1.3296 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0434    1.5953   -1.3577 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3864    2.0373   -0.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7629    0.0762   -1.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0567   -1.5320   -1.9811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7273   -2.8691   -0.3703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5572   -1.2453    1.7103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6253   -1.6406   -0.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4882   -0.1626    2.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8760    3.6710    0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  8 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  5 32  1  0
 32 33  2  0
 32 34  1  0
 34  2  1  0
 30  6  1  0
 26 19  1  0
  3 35  1  0
  4 36  1  0
  6 37  1  1
  8 38  1  1
  9 39  1  0
  9 40  1  0
 13 41  1  0
 17 42  1  0
 19 43  1  1
 21 44  1  0
 21 45  1  0
 22 46  1  6
 23 47  1  0
 24 48  1  6
 25 49  1  0
 26 50  1  6
 27 51  1  0
 28 52  1  6
 29 53  1  0
 30 54  1  6
 31 55  1  0
 34 56  1  0
M  END

HEADER    PROTEIN                                 22-JUN-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-JUN-20         0                                  
HETATM    1  C   UNK     0      -4.621   7.132   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.716   8.377   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.007  18.363   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.043  12.971   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.327  19.869   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.421  12.495   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.153   7.293   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.182  20.900   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667  13.400   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.913  12.495   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.718  20.424   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.437  11.030   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.398  18.917   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.874   9.945   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      -6.779   8.699   0.000  0.00  0.00           N+0
HETATM   16  N   UNK     0      -4.343   9.784   0.000  0.00  0.00           N+0
HETATM   17  O   UNK     0       9.791  20.345   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -7.058   6.047   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       7.503  22.406   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -2.667  14.940   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -5.378  12.971   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.573  21.454   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -6.500  11.352   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       1.352  16.418   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       2.304  13.488   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       2.106  17.255   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       5.119  16.615   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       6.542  17.887   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       0.363  14.477   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -1.897  11.030   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       3.933  18.442   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       3.293  15.429   0.000  0.00  0.00           O+0
HETATM   33  P   UNK     0       1.828  14.953   0.000  0.00  0.00           P+0
HETATM   34  P   UNK     0       3.613  16.935   0.000  0.00  0.00           P+0
HETATM   35  H   UNK     0       8.647  21.376   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.180  14.016   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       6.862  19.393   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.039  14.099   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0      -5.002  11.406   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0       6.038  21.930   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0      -2.738   9.658   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0       4.253  19.948   0.000  0.00  0.00           H+0
CONECT    1    2    7                                                       
CONECT    2    1   16                                                       
CONECT    3    5   28                                                       
CONECT    4    6   29                                                       
CONECT    5    3    8   17   35                                             
CONECT    6    4    9   30   36                                             
CONECT    7    1   15   18                                                  
CONECT    8    5   11   19   37                                             
CONECT    9    6   10   20   38                                             
CONECT   10    9   12   21   39                                             
CONECT   11    8   13   22   40                                             
CONECT   12   10   16   30   41                                             
CONECT   13   11   28   31   42                                             
CONECT   14   15   16   23                                                  
CONECT   15    7   14                                                       
CONECT   16    2   12   14                                                  
CONECT   17    5                                                            
CONECT   18    7                                                            
CONECT   19    8                                                            
CONECT   20    9                                                            
CONECT   21   10                                                            
CONECT   22   11                                                            
CONECT   23   14                                                            
CONECT   24   33                                                            
CONECT   25   33                                                            
CONECT   26   34                                                            
CONECT   27   34                                                            
CONECT   28    3   13                                                       
CONECT   29    4   33                                                       
CONECT   30    6   12                                                       
CONECT   31   13   34                                                       
CONECT   32   33   34                                                       
CONECT   33   24   25   29   32                                             
CONECT   34   26   27   31   32                                             
CONECT   35    5                                                            
CONECT   36    6                                                            
CONECT   37    8                                                            
CONECT   38    9                                                            
CONECT   39   10                                                            
CONECT   40   11                                                            
CONECT   41   12                                                            
CONECT   42   13                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

COMPND    HMDB0012303
HETATM    1  O1  UNL     1      -9.088   2.713   0.689  1.00  0.00           O  
HETATM    2  C1  UNL     1      -8.008   2.086   0.315  1.00  0.00           C  
HETATM    3  C2  UNL     1      -8.025   0.902  -0.263  1.00  0.00           C  
HETATM    4  C3  UNL     1      -6.778   0.301  -0.645  1.00  0.00           C  
HETATM    5  N1  UNL     1      -5.663   0.958  -0.396  1.00  0.00           N  
HETATM    6  C4  UNL     1      -4.435   0.213  -0.355  1.00  0.00           C  
HETATM    7  O2  UNL     1      -3.780  -0.269  -1.403  1.00  0.00           O  
HETATM    8  C5  UNL     1      -2.798  -0.978  -0.718  1.00  0.00           C  
HETATM    9  C6  UNL     1      -1.596  -1.477  -1.407  1.00  0.00           C  
HETATM   10  O3  UNL     1      -0.918  -2.159  -0.298  1.00  0.00           O  
HETATM   11  P1  UNL     1       0.528  -1.420  -0.102  1.00  0.00           P  
HETATM   12  O4  UNL     1       0.800  -0.436  -1.236  1.00  0.00           O  
HETATM   13  O5  UNL     1       0.357  -0.363   1.307  1.00  0.00           O  
HETATM   14  O6  UNL     1       1.872  -2.329   0.266  1.00  0.00           O  
HETATM   15  P2  UNL     1       3.180  -1.335  -0.285  1.00  0.00           P  
HETATM   16  O7  UNL     1       2.814   0.062   0.159  1.00  0.00           O  
HETATM   17  O8  UNL     1       3.081  -1.469  -1.992  1.00  0.00           O  
HETATM   18  O9  UNL     1       4.673  -1.805   0.271  1.00  0.00           O  
HETATM   19  C7  UNL     1       5.395  -0.638   0.546  1.00  0.00           C  
HETATM   20  O10 UNL     1       6.572  -0.912   1.136  1.00  0.00           O  
HETATM   21  C8  UNL     1       7.426   0.133   1.329  1.00  0.00           C  
HETATM   22  C9  UNL     1       6.895   1.455   0.832  1.00  0.00           C  
HETATM   23  O11 UNL     1       6.010   2.034   1.747  1.00  0.00           O  
HETATM   24  C10 UNL     1       6.293   1.348  -0.556  1.00  0.00           C  
HETATM   25  O12 UNL     1       5.316   2.321  -0.635  1.00  0.00           O  
HETATM   26  C11 UNL     1       5.710   0.004  -0.845  1.00  0.00           C  
HETATM   27  O13 UNL     1       6.578  -0.827  -1.503  1.00  0.00           O  
HETATM   28  C12 UNL     1      -3.536  -1.903   0.163  1.00  0.00           C  
HETATM   29  O14 UNL     1      -2.875  -2.106   1.360  1.00  0.00           O  
HETATM   30  C13 UNL     1      -4.813  -1.119   0.373  1.00  0.00           C  
HETATM   31  O15 UNL     1      -5.105  -0.818   1.661  1.00  0.00           O  
HETATM   32  C14 UNL     1      -5.625   2.187   0.190  1.00  0.00           C  
HETATM   33  O16 UNL     1      -4.559   2.776   0.383  1.00  0.00           O  
HETATM   34  N2  UNL     1      -6.876   2.720   0.550  1.00  0.00           N  
HETATM   35  H1  UNL     1      -8.955   0.374  -0.513  1.00  0.00           H  
HETATM   36  H2  UNL     1      -6.822  -0.606  -1.203  1.00  0.00           H  
HETATM   37  H3  UNL     1      -3.741   0.673   0.349  1.00  0.00           H  
HETATM   38  H4  UNL     1      -2.373  -0.129  -0.005  1.00  0.00           H  
HETATM   39  H5  UNL     1      -0.943  -0.761  -1.809  1.00  0.00           H  
HETATM   40  H6  UNL     1      -1.892  -2.294  -2.130  1.00  0.00           H  
HETATM   41  H7  UNL     1       0.136   0.538   1.007  1.00  0.00           H  
HETATM   42  H8  UNL     1       2.862  -2.429  -2.197  1.00  0.00           H  
HETATM   43  H9  UNL     1       4.760   0.043   1.096  1.00  0.00           H  
HETATM   44  H10 UNL     1       8.465  -0.007   0.963  1.00  0.00           H  
HETATM   45  H11 UNL     1       7.523   0.247   2.450  1.00  0.00           H  
HETATM   46  H12 UNL     1       7.754   2.145   0.738  1.00  0.00           H  
HETATM   47  H13 UNL     1       5.227   2.424   1.330  1.00  0.00           H  
HETATM   48  H14 UNL     1       7.043   1.595  -1.358  1.00  0.00           H  
HETATM   49  H15 UNL     1       4.386   2.037  -0.543  1.00  0.00           H  
HETATM   50  H16 UNL     1       4.763   0.076  -1.420  1.00  0.00           H  
HETATM   51  H17 UNL     1       6.057  -1.532  -1.981  1.00  0.00           H  
HETATM   52  H18 UNL     1      -3.727  -2.869  -0.370  1.00  0.00           H  
HETATM   53  H19 UNL     1      -2.557  -1.245   1.710  1.00  0.00           H  
HETATM   54  H20 UNL     1      -5.625  -1.641  -0.158  1.00  0.00           H  
HETATM   55  H21 UNL     1      -4.488  -0.163   2.061  1.00  0.00           H  
HETATM   56  H22 UNL     1      -6.876   3.671   0.997  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   34
CONECT    3    4    4   35
CONECT    4    5   36
CONECT    5    6   32
CONECT    6    7   30   37
CONECT    7    8
CONECT    8    9   28   38
CONECT    9   10   39   40
CONECT   10   11
CONECT   11   12   12   13   14
CONECT   13   41
CONECT   14   15
CONECT   15   16   16   17   18
CONECT   17   42
CONECT   18   19
CONECT   19   20   26   43
CONECT   20   21
CONECT   21   22   44   45
CONECT   22   23   24   46
CONECT   23   47
CONECT   24   25   26   48
CONECT   25   49
CONECT   26   27   50
CONECT   27   51
CONECT   28   29   30   52
CONECT   29   53
CONECT   30   31   54
CONECT   31   55
CONECT   32   33   33   34
CONECT   34   56
END

HMDB0012303
     RDKit          3D
UDP-L-arabinose
 56 58  0  0  0  0  0  0  0  0999 V2000
   -9.0882    2.7129    0.6892 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0080    2.0862    0.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0252    0.9018   -0.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7782    0.3008   -0.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6631    0.9583   -0.3962 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4348    0.2128   -0.3549 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7799   -0.2694   -1.4028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7977   -0.9778   -0.7178 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5962   -1.4774   -1.4067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9184   -2.1589   -0.2981 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5280   -1.4196   -0.1020 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.8003   -0.4356   -1.2360 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3573   -0.3634    1.3073 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8721   -2.3289    0.2655 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1799   -1.3345   -0.2851 P   0  0  0  0  0  5  0  0  0  0  0  0
    2.8141    0.0618    0.1592 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0811   -1.4690   -1.9920 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6734   -1.8048    0.2712 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3947   -0.6377    0.5461 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5723   -0.9115    1.1357 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4260    0.1330    1.3287 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8953    1.4548    0.8323 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0105    2.0342    1.7474 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2927    1.3480   -0.5563 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3160    2.3212   -0.6352 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7096    0.0041   -0.8452 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5783   -0.8267   -1.5032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5360   -1.9029    0.1634 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8754   -2.1060    1.3600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8126   -1.1192    0.3726 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1054   -0.8182    1.6608 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6246    2.1874    0.1903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5591    2.7759    0.3833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8756    2.7198    0.5504 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9548    0.3741   -0.5129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8218   -0.6058   -1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7411    0.6732    0.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3730   -0.1288   -0.0055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9425   -0.7610   -1.8090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8924   -2.2943   -2.1301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365    0.5384    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8621   -2.4294   -2.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7601    0.0433    1.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4648   -0.0068    0.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5226    0.2467    2.4502 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7540    2.1448    0.7382 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2272    2.4240    1.3296 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0434    1.5953   -1.3577 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3864    2.0373   -0.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7629    0.0762   -1.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0567   -1.5320   -1.9811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7273   -2.8691   -0.3703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5572   -1.2453    1.7103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6253   -1.6406   -0.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4882   -0.1626    2.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8760    3.6710    0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  8 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  5 32  1  0
 32 33  2  0
 32 34  1  0
 34  2  1  0
 30  6  1  0
 26 19  1  0
  3 35  1  0
  4 36  1  0
  6 37  1  1
  8 38  1  1
  9 39  1  0
  9 40  1  0
 13 41  1  0
 17 42  1  0
 19 43  1  1
 21 44  1  0
 21 45  1  0
 22 46  1  6
 23 47  1  0
 24 48  1  6
 25 49  1  0
 26 50  1  6
 27 51  1  0
 28 52  1  6
 29 53  1  0
 30 54  1  6
 31 55  1  0
 34 56  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
UDP-beta-L-Arabinose	ChEBI
UDP-beta-L-Arap	ChEBI
Uridine 5'-diphospho-beta-L-arabinopyranose	ChEBI
UDP-b-L-Arabinose	Generator
UDP-Β-L-arabinose	Generator
UDP-b-L-Arap	Generator
UDP-Β-L-arap	Generator
Uridine 5'-diphospho-b-L-arabinopyranose	Generator
Uridine 5'-diphospho-β-L-arabinopyranose	Generator
UDP-b-L-Arabinopyranose	Generator
UDP-β-L-arabinopyranose	Generator
UDP-L-arabinose	HMDB
UDP-arabinose	HMDB
UDP-beta-L-arabinopyranose	HMDB
Uridine 5'-(trihydrogen diphosphate) mono-L-arabinopyranosyl ester	HMDB
Uridine 5'-(trihydrogen pyrophosphate) mono-L-arabinopyranosyl ester	HMDB
Uridine 5'-(trihydrogen pyrophosphate) mono-L-arabinosyl ester	HMDB
Uridine 5'-diphosphate arabinoside	HMDB
Uridine 5'-pyrophosphate, beta-L-arabinosyl ester	HMDB
Uridine 5'-pyrophosphate, β-L-arabinosyl ester	HMDB
Uridine 5’-(trihydrogen diphosphate) mono-L-arabinopyranosyl ester	HMDB
Uridine 5’-(trihydrogen pyrophosphate) mono-L-arabinopyranosyl ester	HMDB
Uridine 5’-(trihydrogen pyrophosphate) mono-L-arabinosyl ester	HMDB
Uridine 5’-diphosphate arabinoside	HMDB
Uridine 5’-pyrophosphate, β-L-arabinosyl ester	HMDB
Uridine diphosphate arabinose	HMDB
Uridine diphospho-beta-L-arabinopyranose	HMDB
Uridine diphospho-β-L-arabinopyranose	HMDB
Uridine diphosphoarabinose	HMDB

Chemical Formula

C₁₄H₂₂N₂O₁₆P₂

Average Molecular Weight

536.2758

Monoisotopic Molecular Weight

536.04445569

IUPAC Name

{[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-hydroxy-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}({[hydroxy({[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy})phosphoryl]oxy})phosphinic acid

Traditional Name

[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-hydroxy-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy([hydroxy([(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy)phosphoryl]oxy)phosphinic acid

CAS Registry Number

15839-78-8

SMILES

O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O

InChI Identifier

InChI=1S/C14H22N2O16P2/c17-5-3-28-13(11(22)8(5)19)31-34(26,27)32-33(24,25)29-4-6-9(20)10(21)12(30-6)16-2-1-7(18)15-14(16)23/h1-2,5-6,8-13,17,19-22H,3-4H2,(H,24,25)(H,26,27)(H,15,18,23)/t5-,6+,8-,9+,10+,11+,12+,13+/m0/s1

InChI Key

DQQDLYVHOTZLOR-IAZOVDBXSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrimidine ribonucleoside diphosphates. These are pyrimidine ribonucleotides with diphosphate group linked to the ribose moiety.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Sub Class

Pyrimidine ribonucleotides

Direct Parent

Pyrimidine ribonucleoside diphosphates

Alternative Parents

Substituents

Pyrimidine ribonucleoside diphosphate
Pentose phosphate
Pentose-5-phosphate
Glycosyl compound
N-glycosyl compound
Monosaccharide phosphate
Organic pyrophosphate
Pyrimidone
Monoalkyl phosphate
Hydropyrimidine
Monosaccharide
Organic phosphoric acid derivative
Oxane
Phosphoric acid ester
Pyrimidine
Alkyl phosphate
Vinylogous amide
Heteroaromatic compound
Tetrahydrofuran
Lactam
Urea
Secondary alcohol
Oxacycle
Polyol
Organoheterocyclic compound
Azacycle
Alcohol
Organic nitrogen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

UDP-L-arabinose (CHEBI:61455 )

Ontology

Not Available

Endogenous (HMDB: HMDB0012303)

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Nut

Peanut (FooDB: FOOD00016)
Cashew nut (FooDB: FOOD00011)
Brazil nut (FooDB: FOOD00024)
Pecan nut (FooDB: FOOD00044)
Chestnut (FooDB: FOOD00045)
Common hazelnut (FooDB: FOOD00062)
Black walnut (FooDB: FOOD00093)
Common walnut (FooDB: FOOD00094)
Pine nut (FooDB: FOOD00138)
Pistachio (FooDB: FOOD00140)
Almond (FooDB: FOOD00148)
Macadamia nut (M. tetraphylla) (FooDB: FOOD00225)
Japanese walnut (FooDB: FOOD00240)
Acorn (FooDB: FOOD00282)
Beech nut (FooDB: FOOD00299)
Butternut (FooDB: FOOD00316)
Chinese chestnut (FooDB: FOOD00331)
European chestnut (FooDB: FOOD00363)
Hazelnut (FooDB: FOOD00376)
Hickory nut (FooDB: FOOD00377)
Japanese chestnut (FooDB: FOOD00385)
Pili nut (FooDB: FOOD00432)
Colorado pinyon (FooDB: FOOD00433)
Macadamia nut (FooDB: FOOD00525)
Walnut (FooDB: FOOD00608)

Herb and spice mixture

Curry powder (FooDB: FOOD00678)

Vegetable

Cabbage

Onion-family vegetable

Root vegetable

Shoot vegetable

Leaf vegetable

Common beet (FooDB: FOOD00025)
Endive (FooDB: FOOD00048)
Rocket salad (ssp.) (FooDB: FOOD00077)
Swamp cabbage (FooDB: FOOD00091)
Lettuce (FooDB: FOOD00095)
Garden cress (FooDB: FOOD00099)
Spinach (FooDB: FOOD00178)
Swiss chard (FooDB: FOOD00237)
Chicory leaves (FooDB: FOOD00250)
Garland chrysanthemum (FooDB: FOOD00333)
Corn salad (FooDB: FOOD00340)
Jute (FooDB: FOOD00389)
Lambsquarters (FooDB: FOOD00394)
Malabar spinach (FooDB: FOOD00404)
New Zealand spinach (FooDB: FOOD00415)
Yautia (FooDB: FOOD00510)
Ostrich fern (FooDB: FOOD00556)
Romaine lettuce (FooDB: FOOD00888)
Iceberg lettuce (FooDB: FOOD00973)
Pea shoots (FooDB: FOOD00975)
Yau choy (FooDB: FOOD00976)
Water spinach (FooDB: FOOD00977)

Fruit vegetable

Pepper (FooDB: FOOD00040)
Olive (FooDB: FOOD00121)
Avocado (FooDB: FOOD00130)
Garden tomato (FooDB: FOOD00171)
Cherry tomato (FooDB: FOOD00172)
Garden tomato (var.) (FooDB: FOOD00173)
Eggplant (FooDB: FOOD00174)
Pepper (C. baccatum) (FooDB: FOOD00231)
Pepper (C. chinense) (FooDB: FOOD00232)
Pepper (Capsicum) (FooDB: FOOD00233)
Groundcherry (FooDB: FOOD00371)
Pepper (C. frutescens) (FooDB: FOOD00428)
Mexican groundcherry (FooDB: FOOD00491)
Pepper (C. pubescens) (FooDB: FOOD00849)
Green bell pepper (FooDB: FOOD00877)
Yellow bell pepper (FooDB: FOOD00878)
Orange bell pepper (FooDB: FOOD00879)
Red bell pepper (FooDB: FOOD00880)
Italian sweet red pepper (FooDB: FOOD00881)
Jalapeno pepper (FooDB: FOOD00955)
Cubanelle pepper (FooDB: FOOD00971)

Tuber

Stalk vegetable

Other vegetable

Giant butterbur (FooDB: FOOD00314)
Carob (FooDB: FOOD00321)
Chinese water chestnut (FooDB: FOOD00332)
Horseradish tree (FooDB: FOOD00379)
Sacred lotus (FooDB: FOOD00402)
Nopal (FooDB: FOOD00416)
Okra (FooDB: FOOD00420)
Sesbania flower (FooDB: FOOD00469)
Agave (FooDB: FOOD00563)
Narrowleaf cattail (FooDB: FOOD00564)
Heart of palm (FooDB: FOOD00718)
Tree fern (FooDB: FOOD00797)

Mushroom

Castanospermum australe (FooDB: FOOD00893)
Gentiana lutea (FooDB: FOOD00894)
Juniperus communis (FooDB: FOOD00895)
Albizia gummifera (FooDB: FOOD00896)

Fruit

Tropical fruit

Citrus

Lime (FooDB: FOOD00053)
Lemon (FooDB: FOOD00054)
Pummelo (FooDB: FOOD00055)
Mandarin orange (Clementine, Tangerine) (FooDB: FOOD00056)
Sweet orange (FooDB: FOOD00057)
Grapefruit/Pummelo hybrid (FooDB: FOOD00255)
Grapefruit (FooDB: FOOD00256)
Persian lime (FooDB: FOOD00543)
Sour orange (FooDB: FOOD00918)
Mikan (FooDB: FOOD00932)
Clementine (FooDB: FOOD00959)

Pome

Berry

Black crowberry (FooDB: FOOD00075)
Strawberry (FooDB: FOOD00083)
Black huckleberry (FooDB: FOOD00084)
Sea-buckthornberry (FooDB: FOOD00087)
Mulberry (FooDB: FOOD00116)
Black mulberry (FooDB: FOOD00117)
Black chokeberry (FooDB: FOOD00136)
Blackcurrant (FooDB: FOOD00155)
Redcurrant (FooDB: FOOD00156)
Gooseberry (FooDB: FOOD00157)
Cloudberry (FooDB: FOOD00161)
Red raspberry (FooDB: FOOD00162)
Black raspberry (FooDB: FOOD00163)
Black elderberry (FooDB: FOOD00166)
Rowanberry (FooDB: FOOD00176)
Vaccinium (Blueberry, Cranberry, Huckleberry) (FooDB: FOOD00188)
Lowbush blueberry (FooDB: FOOD00189)
Sparkleberry (FooDB: FOOD00190)
Highbush blueberry (FooDB: FOOD00191)
American cranberry (FooDB: FOOD00192)
Bilberry (FooDB: FOOD00193)
Lingonberry (FooDB: FOOD00194)
Muscadine grape (FooDB: FOOD00203)
Common grape (FooDB: FOOD00204)
Arctic blackberry (FooDB: FOOD00207)
Bayberry (FooDB: FOOD00209)
Elliott's blueberry (FooDB: FOOD00210)
Canada blueberry (FooDB: FOOD00211)
Bog bilberry (FooDB: FOOD00212)
Buffalo currant (FooDB: FOOD00213)
European cranberry (FooDB: FOOD00217)
Deerberry (FooDB: FOOD00218)
Cascade huckleberry (FooDB: FOOD00220)
Oval-leaf huckleberry (FooDB: FOOD00221)
Evergreen huckleberry (FooDB: FOOD00222)
Red huckleberry (FooDB: FOOD00223)
Summer grape (FooDB: FOOD00227)
Fox grape (FooDB: FOOD00228)
Half-highbush blueberry (FooDB: FOOD00248)
Jostaberry (FooDB: FOOD00257)
Sweet rowanberry (FooDB: FOOD00265)
Skunk currant (FooDB: FOOD00267)
Squashberry (FooDB: FOOD00344)
Elderberry (FooDB: FOOD00358)
Grape (FooDB: FOOD00369)
Alaska blueberry (FooDB: FOOD00380)
Loganberry (FooDB: FOOD00400)
Ohelo berry (FooDB: FOOD00419)
Salmonberry (FooDB: FOOD00456)
Strawberry guava (FooDB: FOOD00482)
Boysenberry (FooDB: FOOD00542)
Chinese bayberry (FooDB: FOOD00852)
Saskatoon berry (FooDB: FOOD00884)
Nanking cherry (FooDB: FOOD00885)
Rabbiteye blueberry (FooDB: FOOD00898)
Blackberry (FooDB: FOOD00906)
Partridge berry (FooDB: FOOD00931)
Green grape (FooDB: FOOD00964)
Red grape (FooDB: FOOD00965)
Black plum (FooDB: FOOD00966)
Black raisin (FooDB: FOOD00968)
Chinese plum (FooDB: FOOD00978)
Green plum (FooDB: FOOD00979)
Wampee (FooDB: FOOD00980)
Goji (FooDB: FOOD00982)
Monk fruit (FooDB: FOOD00983)
Hawthorn (FooDB: FOOD00985)
Lantern fruit (FooDB: FOOD00986)
Cape gooseberry (FooDB: FOOD00988)

Other fruit

Fig (FooDB: FOOD00081)
Date (FooDB: FOOD00135)
Jujube (FooDB: FOOD00388)

Drupe

Prunus (Cherry, Plum) (FooDB: FOOD00143)
Apricot (FooDB: FOOD00144)
Sweet cherry (FooDB: FOOD00145)
Sour cherry (FooDB: FOOD00146)
European plum (FooDB: FOOD00147)
Peach (FooDB: FOOD00149)
Nectarine (FooDB: FOOD00229)
Peach (var.) (FooDB: FOOD00230)
Common chokecherry (FooDB: FOOD00562)

Cereal and cereal product

Cereal

Cereal product

Pasta (FooDB: FOOD00273)
Bulgur (FooDB: FOOD00741)
Semolina (FooDB: FOOD00745)
Flour (FooDB: FOOD00799)

Dough

Sourdough (FooDB: FOOD00275)

Leavened bread

Flat bread

Other bread

Potato bread (FooDB: FOOD00811)

Sweet bread

Raisin bread (FooDB: FOOD00817)

Pulse

Pea

Lentil

Lentils (FooDB: FOOD00098)

Other pulse

Lupine (FooDB: FOOD00104)
White lupine (FooDB: FOOD00403)

Bean

Green lentil (FooDB: FOOD00970)

Gourd

Watermelon (FooDB: FOOD00052)
Muskmelon (FooDB: FOOD00064)
Cucumber (FooDB: FOOD00065)
Cucurbita (FooDB: FOOD00066)
Bitter gourd (FooDB: FOOD00115)
Winter squash (FooDB: FOOD00283)
Butternut squash (FooDB: FOOD00317)
Calabash (FooDB: FOOD00318)
Chayote (FooDB: FOOD00325)
Towel gourd (FooDB: FOOD00492)
Wax gourd (FooDB: FOOD00499)
Tinda (FooDB: FOOD00559)
Horned melon (FooDB: FOOD00761)
Sunburst squash (pattypan squash) (FooDB: FOOD00874)
Green zucchini (FooDB: FOOD00875)
Yellow zucchini (FooDB: FOOD00876)
Japanese pumpkin (FooDB: FOOD00886)
Acorn squash (FooDB: FOOD00972)
Cantaloupe melon (FooDB: FOOD00984)

Coffee and coffee product

Coffee

Arabica coffee (FooDB: FOOD00059)
Robusta coffee (FooDB: FOOD00060)

Soy

Soy bean (FooDB: FOOD00085)

Soy product

Soy sauce (FooDB: FOOD00694)
Miso (FooDB: FOOD00695)
Tofu (FooDB: FOOD00696)
Soy milk (FooDB: FOOD00736)
Soy cream (FooDB: FOOD00784)

Dish

Other dish

Taco shell (FooDB: FOOD00991)
Tostada shell (FooDB: FOOD00992)

Tea

Herbal tea

Hibiscus tea (FooDB: FOOD00723)
Greenthread tea (FooDB: FOOD00820)

Baking good

Wrapper

Wonton wrapper (FooDB: FOOD00818)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	13.6 g/L	ALOGPS
logP	-1.2	ALOGPS
logP	-4	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	1.73	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	274.8 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	100.82 m³·mol⁻¹	ChemAxon
Polarizability	43.61 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	214.853	31661259
DarkChem	[M-H]-	204.196	31661259
DeepCCS	[M+H]+	197.323	30932474
DeepCCS	[M-H]-	195.498	30932474
DeepCCS	[M-2H]-	228.734	30932474
DeepCCS	[M+Na]+	202.929	30932474
AllCCS	[M+H]+	208.3	32859911
AllCCS	[M+H-H2O]+	206.6	32859911
AllCCS	[M+NH4]+	209.8	32859911
AllCCS	[M+Na]+	210.2	32859911
AllCCS	[M-H]-	200.6	32859911
AllCCS	[M+Na-2H]-	201.3	32859911
AllCCS	[M+HCOO]-	202.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
UDP-L-arabinose	O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O	4576.3	Standard polar	33892256
UDP-L-arabinose	O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O	3106.5	Standard non polar	33892256
UDP-L-arabinose	O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O	4539.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
UDP-L-arabinose,1TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4037.7	Semi standard non polar	33892256
UDP-L-arabinose,1TMS,isomer #2	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O	4039.5	Semi standard non polar	33892256
UDP-L-arabinose,1TMS,isomer #3	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O	3992.4	Semi standard non polar	33892256
UDP-L-arabinose,1TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O	4015.4	Semi standard non polar	33892256
UDP-L-arabinose,1TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)[NH]C1=O	4029.9	Semi standard non polar	33892256
UDP-L-arabinose,1TMS,isomer #6	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O	4123.1	Semi standard non polar	33892256
UDP-L-arabinose,1TMS,isomer #7	C[Si](C)(C)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O	4133.9	Semi standard non polar	33892256
UDP-L-arabinose,1TMS,isomer #8	C[Si](C)(C)N1C(=O)C=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3OC[C@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C1=O	4138.2	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #1	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	3900.5	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #10	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	3872.8	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #11	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O	3991.5	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #12	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O	3984.2	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #13	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O	4068.1	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #14	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O	3846.2	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #15	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C	3874.6	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #16	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O	3935.3	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #17	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O	3929.5	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #18	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@@H]1O	4010.7	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #19	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O	3869.6	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #2	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H]1O	3855.6	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #20	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O	3960.5	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #21	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3951.6	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #22	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O	4034.0	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #23	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)[NH]C1=O	3959.0	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #24	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(=O)[NH]C1=O	3969.8	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #25	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O	4044.3	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #26	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C	4056.0	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #27	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O	4109.5	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #28	C[Si](C)(C)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O	4123.2	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3877.4	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C	3905.7	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3972.2	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3980.1	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	4049.1	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #8	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O	3889.2	Semi standard non polar	33892256
UDP-L-arabinose,2TMS,isomer #9	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	3881.8	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #1	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	3777.3	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O	3804.8	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #11	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H]1O	3889.8	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3768.3	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #13	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3814.4	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #14	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3820.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3899.2	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #16	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C	3839.1	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #17	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C	3849.2	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #18	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C	3931.4	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #19	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3888.8	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #2	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3759.0	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #20	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3981.6	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #21	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3981.7	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #22	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	3751.3	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #23	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	3742.8	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #24	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O	3830.0	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #25	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O	3825.4	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #26	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O	3925.7	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #27	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3787.0	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #28	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	3820.1	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #29	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3816.0	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3749.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #30	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	3912.1	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #31	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	3815.5	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #32	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3805.4	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #33	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	3912.3	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #34	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O	3894.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #35	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O	4006.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #36	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O	4006.3	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #37	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C	3757.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #38	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O	3807.3	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #39	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O	3797.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #4	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	3834.4	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #40	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O	3882.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #41	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C	3827.6	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #42	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3816.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #43	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C	3901.5	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #44	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O	3860.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #45	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@@H]1O	3951.8	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #46	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O	3945.0	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #47	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O	3817.8	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #48	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	3811.0	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #49	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O	3892.4	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #5	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O	3830.7	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #50	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3868.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #51	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O	3967.7	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #52	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3962.4	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #53	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(=O)[NH]C1=O	3887.1	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #54	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O	3972.4	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #55	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O	3976.5	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #56	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C	4035.2	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #6	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	3933.4	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #7	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O	3754.9	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3764.3	Semi standard non polar	33892256
UDP-L-arabinose,3TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H]1O	3814.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #1	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3713.1	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3754.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3769.0	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3830.4	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #13	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O	3825.4	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #14	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	3889.1	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #15	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O	3892.6	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #16	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3714.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #17	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O	3766.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #18	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O	3752.6	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #19	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O	3838.4	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #2	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3710.6	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #20	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3761.2	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #21	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3775.0	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #22	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3839.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #23	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O	3817.0	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #24	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H]1O	3877.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #25	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O	3877.4	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #26	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3758.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #27	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	3750.4	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #28	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3835.7	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #29	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3809.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #3	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	3773.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #30	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3869.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #31	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3867.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #32	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C	3820.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #33	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C	3893.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #34	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C	3890.3	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #35	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3925.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #36	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3719.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #37	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	3758.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #38	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3750.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #39	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	3825.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #4	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O	3765.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #40	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	3759.1	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #41	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3745.1	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #42	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	3823.7	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #43	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O	3822.2	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #44	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O	3885.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #45	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O	3888.7	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #46	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3787.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #47	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3776.1	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #48	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3862.4	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #49	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3818.2	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #5	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	3852.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #50	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	3877.3	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #51	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3877.6	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #52	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3817.0	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #53	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	3878.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #54	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3873.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #55	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O	3935.4	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #56	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C	3768.1	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #57	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3754.4	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #58	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C	3832.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #59	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O	3811.4	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #6	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3727.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #60	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O	3871.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #61	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O	3870.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #62	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3817.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #63	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C	3879.7	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #64	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3877.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #65	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O	3918.5	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #66	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	3805.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #67	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O	3865.0	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #68	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	3865.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #69	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3913.8	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #7	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3767.7	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #70	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O	3923.9	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #8	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3759.2	Semi standard non polar	33892256
UDP-L-arabinose,4TMS,isomer #9	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3831.8	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #1	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3711.6	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #10	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O	3870.9	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #11	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3759.4	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #12	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3747.9	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #13	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3846.3	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #14	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3781.6	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #15	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3867.5	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #16	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3865.7	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #17	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3790.1	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #18	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3869.6	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #19	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3875.8	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #2	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3739.4	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #20	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O	3909.9	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #21	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3743.3	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #22	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3733.0	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #23	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3832.3	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #24	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O	3774.5	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #25	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O	3871.4	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #26	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O	3864.6	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #27	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	3784.4	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #28	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3871.2	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #29	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3875.9	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #3	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3730.6	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #30	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O	3911.5	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #31	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	3749.9	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #32	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3852.3	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #33	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)O[Si](C)(C)C	3848.1	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #34	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O	3892.1	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #35	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C	3898.9	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #36	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3752.5	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #37	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3739.2	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #38	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3835.3	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #39	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3770.9	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #4	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3829.7	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #40	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O	3854.6	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #41	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3854.4	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #42	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3777.0	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #43	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	3862.4	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #44	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3856.3	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #45	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O	3900.9	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #46	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3778.6	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #47	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3883.3	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #48	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3878.1	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #49	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3899.5	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #5	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3749.3	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #50	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3902.2	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #51	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3775.8	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #52	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C	3864.9	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #53	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3859.8	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #54	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O	3899.3	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #55	C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3900.2	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #56	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](O[Si](C)(C)C)[C@@H]1O)O[Si](C)(C)C	3883.1	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #6	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3735.1	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #7	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3833.5	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #8	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H]1O	3771.8	Semi standard non polar	33892256
UDP-L-arabinose,5TMS,isomer #9	C[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C)C3=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	3871.7	Semi standard non polar	33892256
UDP-L-arabinose,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4252.3	Semi standard non polar	33892256
UDP-L-arabinose,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O	4231.3	Semi standard non polar	33892256
UDP-L-arabinose,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O	4201.5	Semi standard non polar	33892256
UDP-L-arabinose,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O	4215.1	Semi standard non polar	33892256
UDP-L-arabinose,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)[NH]C1=O	4250.3	Semi standard non polar	33892256
UDP-L-arabinose,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O	4325.3	Semi standard non polar	33892256
UDP-L-arabinose,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O	4339.2	Semi standard non polar	33892256
UDP-L-arabinose,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N1C(=O)C=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)O[C@H]3OC[C@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H]2O)C1=O	4366.3	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4303.8	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4248.7	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O	4360.3	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4354.3	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O	4431.5	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O	4260.1	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	4266.7	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O	4330.8	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H]1O	4314.2	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@@H]1O	4387.8	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4271.3	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	4269.2	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O	4334.0	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	4320.2	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O	4399.4	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)[NH]C1=O	4362.9	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(=O)[NH]C1=O	4369.6	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O	4434.6	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4422.3	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O)OP(=O)(O)O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O	4484.4	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O	4492.6	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4276.4	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C	4316.1	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4365.3	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4372.6	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O	4434.3	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O	4296.8	Semi standard non polar	33892256
UDP-L-arabinose,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4259.5	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4407.5	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O	4423.6	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	4493.0	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4377.0	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4414.4	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4424.5	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O	4492.4	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C	4455.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C	4458.4	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C	4533.1	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4491.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4379.3	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O	4557.5	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O	4558.7	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4379.4	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4372.3	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O	4446.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4442.1	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H]1O	4523.4	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4371.6	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4418.1	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4410.2	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4373.7	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4480.2	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4412.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4395.9	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4468.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4478.4	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@H](O)[C@H]1O	4544.9	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4545.7	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	4388.2	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O	4437.0	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H]1O	4421.9	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4446.4	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H]1O	4496.5	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	4430.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4416.1	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	4479.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H]1O	4462.7	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)[C@@H]1O	4526.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H]1O	4513.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4427.6	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)O[Si](C)(C)C(C)(C)C	4416.2	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4496.3	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4441.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	4459.2	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O	4523.0	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O)CO[C@@H]1OP(=O)(O)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	4515.7	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #53	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(=O)[NH]C1=O	4492.7	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #54	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O	4561.0	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]2OC[C@H](O)[C@H](O)[C@H]2O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O	4561.2	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #56	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](O)[C@@H]1O)OP(=O)(O[C@H]1OC[C@H](O)[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4576.8	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@H]1CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4519.2	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	4396.4	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]2OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1O	4389.0	Semi standard non polar	33892256
UDP-L-arabinose,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(=O)[NH]C3=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	4439.5	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 - UDP-L-arabinose GC-MS (Non-derivatized) - 70eV, Positive	splash10-016r-4936760000-00f37a38fe624376e23d	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (2 TMS) - 70eV, Positive	splash10-0300-4642229000-26e6ed2c6eb4497585c2	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-10-13	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - UDP-L-arabinose GC-MS (TMS_2_16) - 70eV, Positive	Not Available	2021-10-13	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 - UDP-L-arabinose 10V, Positive-QTOF	splash10-03di-0901110000-8ae0db777cff3d445c4c	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 20V, Positive-QTOF	splash10-03di-4910000000-67006286cf564f62ff42	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 40V, Positive-QTOF	splash10-03di-5900000000-da262c67a1973399a755	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 10V, Negative-QTOF	splash10-000f-8713790000-946e0081f7ad1a09d3d6	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 20V, Negative-QTOF	splash10-01ox-9622010000-7089747eea74980128f4	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 40V, Negative-QTOF	splash10-06tf-4900000000-53eebd3beb66a7fd8d3f	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 10V, Negative-QTOF	splash10-000i-0001090000-5cb9330b784831a318c0	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 20V, Negative-QTOF	splash10-0btc-5913210000-b3ea7476b5c2e48ecb1f	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 40V, Negative-QTOF	splash10-0a4l-4956200000-d7160be3d1a922677c83	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 10V, Positive-QTOF	splash10-03dr-1800690000-ee1b02fe5fb340e69a4b	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 20V, Positive-QTOF	splash10-03di-4961210000-998fdbdb53c26f8dfaa2	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - UDP-L-arabinose 40V, Positive-QTOF	splash10-03ea-5921000000-c5798a971977016536d7	2021-09-25	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

FDB028926

KNApSAcK ID

Not Available

Chemspider ID

559145

KEGG Compound ID

C00935

BioCyc ID

CPD-12513

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

644105

PDB ID

Not Available

ChEBI ID

61455

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 UDP-L-arabinose (HMDB0012303)

MOL for HMDB0012303 (UDP-L-arabinose)

3D MOL for HMDB0012303 (UDP-L-arabinose)

3D SDF for HMDB0012303 (UDP-L-arabinose)

3D-SDF for HMDB0012303 (UDP-L-arabinose)

PDB for HMDB0012303 (UDP-L-arabinose)

3D PDB for HMDB0012303 (UDP-L-arabinose)

SMILES for HMDB0012303 (UDP-L-arabinose)

INCHI for HMDB0012303 (UDP-L-arabinose)

Structure for HMDB0012303 (UDP-L-arabinose)

3D Structure for HMDB0012303 (UDP-L-arabinose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra