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Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2021-09-14 15:48:15 UTC

HMDB ID

HMDB0001397

Secondary Accession Numbers

HMDB01397

Metabolite Identification

Common Name

Guanosine monophosphate

Description

Guanosine monophosphate (GMP), also known as 5′-guanidylic acid or guanylic acid (conjugate base guanylate), is a nucleotide that is used as a monomer in RNA. It is an ester of phosphoric acid with the nucleoside guanosine. GMP consists of the phosphate group, the pentose sugar ribose, and the nucleobase guanine; hence it is a ribonucleoside monophosphate. Guanosine monophosphate is commercially produced by microbial fermentation. Guanosine monophosphate, also known as guanylic acid or 5'-GMP, belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached. A guanine nucleotide containing one phosphate group esterified to the sugar moiety and found widely in nature. Guanosine monophosphate exists in all living species, ranging from bacteria to humans. Within humans, guanosine monophosphate participates in a number of enzymatic reactions. In particular, guanosine triphosphate and guanosine monophosphate can be biosynthesized from diguanosine tetraphosphate through its interaction with the enzyme bis(5'-nucleosyl)-tetraphosphatase [asymmetrical]. In addition, guanosine monophosphate can be biosynthesized from guanosine diphosphate; which is mediated by the enzyme ectonucleoside triphosphate diphosphohydrolase 5. In humans, guanosine monophosphate is involved in the metabolic disorder called the lesch-nyhan syndrome (lns) pathway. Outside of the human body, guanosine monophosphate has been detected, but not quantified in several different foods, such as common cabbages, tea, winter squash, spearmints, and sugar apples.

Structure

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

HMDB0001397
     RDKit          3D
Guanosine monophosphate
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.8188   -0.6570   -2.0425 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2468    0.1029   -0.9763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0314   -0.1991   -0.4791 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5523    0.5514    0.5192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2813    1.6024    1.0237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5373    2.1485    2.0025 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4022    1.4782    2.1086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3955    0.4775    1.1895 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2830   -0.4247    1.0673 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9494    0.2612    0.9968 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8143   -0.7852    0.7138 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2122   -0.3230    0.3951 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2767    0.5149   -0.6995 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9100    0.9350   -0.9133 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.7008   -0.2504   -1.4633 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0768    2.2544   -1.9457 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6188    1.3295    0.5717 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1582   -1.4365   -0.4823 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5296   -2.7476   -0.6625 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3287   -1.3020   -0.1247 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7602   -2.5751    0.2323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5292    1.9140    0.5145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2034    2.8731    0.9691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9839    1.1298   -0.4993 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5625   -1.6572   -2.1905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4998   -0.2376   -2.6941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242    1.7215    2.8297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2274   -1.0266    2.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8553   -1.4414    1.5872 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8102   -1.2271    0.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6231    0.1647    1.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6455    2.9752   -1.5708 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0689    0.5395    0.9821 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4057   -0.7942   -1.3667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9402   -3.0991    0.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8188   -0.8986   -1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5833   -3.2499   -0.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9257    1.3589   -0.8891 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 14 17  1  0
 11 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
  5 22  1  0
 22 23  2  0
 22 24  1  0
 24  2  1  0
  8  4  1  0
 20  9  1  0
  1 25  1  0
  1 26  1  0
  7 27  1  0
  9 28  1  1
 11 29  1  1
 12 30  1  0
 12 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  6
 19 35  1  0
 20 36  1  6
 21 37  1  0
 24 38  1  0
M  END

  Mrv1652309042000222D          

 24 26  0  0  1  0            999 V2000
    1.4657    0.1111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8336    0.5557    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2020    0.6564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5456   -0.7329    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0695    0.3022    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1183    1.3823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9797    1.3789    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9453    0.3230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3306   -1.0767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6043    0.8127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1875   -0.4411    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0426   -0.5592    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6052    0.8162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4209   -1.8999    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2608    0.3369    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0108   -0.4411    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2952   -1.1115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0457    0.5974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2712   -1.2226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6675    0.0417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4941    0.0417    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4975   -0.7849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208    0.0417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4975    0.8683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  2  0  0  0  0
  1  4  1  0  0  0  0
  5  2  1  1  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  3  8  1  0  0  0  0
  4  9  2  0  0  0  0
  5 10  1  0  0  0  0
  5 11  1  0  0  0  0
  8 12  1  0  0  0  0
  8 13  2  0  0  0  0
  9 14  1  0  0  0  0
 10 15  1  0  0  0  0
 11 16  1  0  0  0  0
 11 17  1  6  0  0  0
 15 18  1  1  0  0  0
 16 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  2  0  0  0  0
  6  7  2  0  0  0  0
  9 12  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0001397

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)C(=O)N1

> <INCHI_IDENTIFIER>
InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1

> <INCHI_KEY>
RQFCJASXJCIDSX-UUOKFMHZSA-N

> <FORMULA>
C10H14N5O8P

> <MOLECULAR_WEIGHT>
363.2206

> <EXACT_MASS>
363.057998961

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
30.69674158026033

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4R,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

> <ALOGPS_LOGP>
-1.99

> <JCHEM_LOGP>
-3.1266968802741064

> <ALOGPS_LOGS>
-2.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.250470034590121

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.291332123072766

> <JCHEM_PKA_STRONGEST_BASIC>
0.3777087267091779

> <JCHEM_POLAR_SURFACE_AREA>
201.74999999999994

> <JCHEM_REFRACTIVITY>
75.49399999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.56e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
guanylate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0001397
     RDKit          3D
Guanosine monophosphate
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.8188   -0.6570   -2.0425 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2468    0.1029   -0.9763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0314   -0.1991   -0.4791 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5523    0.5514    0.5192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2813    1.6024    1.0237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5373    2.1485    2.0025 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4022    1.4782    2.1086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3955    0.4775    1.1895 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2830   -0.4247    1.0673 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9494    0.2612    0.9968 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8143   -0.7852    0.7138 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2122   -0.3230    0.3951 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2767    0.5149   -0.6995 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9100    0.9350   -0.9133 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.7008   -0.2504   -1.4633 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0768    2.2544   -1.9457 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6188    1.3295    0.5717 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1582   -1.4365   -0.4823 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5296   -2.7476   -0.6625 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3287   -1.3020   -0.1247 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7602   -2.5751    0.2323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5292    1.9140    0.5145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2034    2.8731    0.9691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9839    1.1298   -0.4993 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5625   -1.6572   -2.1905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4998   -0.2376   -2.6941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242    1.7215    2.8297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2274   -1.0266    2.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8553   -1.4414    1.5872 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8102   -1.2271    0.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6231    0.1647    1.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6455    2.9752   -1.5708 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0689    0.5395    0.9821 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4057   -0.7942   -1.3667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9402   -3.0991    0.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8188   -0.8986   -1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5833   -3.2499   -0.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9257    1.3589   -0.8891 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 14 17  1  0
 11 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
  5 22  1  0
 22 23  2  0
 22 24  1  0
 24  2  1  0
  8  4  1  0
 20  9  1  0
  1 25  1  0
  1 26  1  0
  7 27  1  0
  9 28  1  1
 11 29  1  1
 12 30  1  0
 12 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  6
 19 35  1  0
 20 36  1  6
 21 37  1  0
 24 38  1  0
M  END

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  C   UNK     0       2.736   0.207   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       1.556   1.037   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       4.110   1.225   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       2.885  -1.368   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       0.130   0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.087   2.580   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       3.695   2.574   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       5.498   0.603   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.350  -2.010   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.128   1.517   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.350  -0.823   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       5.680  -1.044   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0       6.730   1.524   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       4.519  -3.546   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -2.353   0.629   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.887  -0.823   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.551  -2.075   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.819   1.115   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.373  -2.282   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -4.979   0.078   0.000  0.00  0.00           O+0
HETATM   21  P   UNK     0      -6.522   0.078   0.000  0.00  0.00           P+0
HETATM   22  O   UNK     0      -6.529  -1.465   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -8.065   0.078   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -6.529   1.621   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7    8                                                  
CONECT    4    1    9                                                       
CONECT    5    2   10   11                                                  
CONECT    6    2    7                                                       
CONECT    7    3    6                                                       
CONECT    8    3   12   13                                                  
CONECT    9    4   14   12                                                  
CONECT   10    5   15                                                       
CONECT   11    5   16   17                                                  
CONECT   12    8    9                                                       
CONECT   13    8                                                            
CONECT   14    9                                                            
CONECT   15   10   18   16                                                  
CONECT   16   11   19   15                                                  
CONECT   17   11                                                            
CONECT   18   15   20                                                       
CONECT   19   16                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

COMPND    HMDB0001397
HETATM    1  N1  UNL     1      -4.819  -0.657  -2.043  1.00  0.00           N  
HETATM    2  C1  UNL     1      -4.247   0.103  -0.976  1.00  0.00           C  
HETATM    3  N2  UNL     1      -3.031  -0.199  -0.479  1.00  0.00           N  
HETATM    4  C2  UNL     1      -2.552   0.551   0.519  1.00  0.00           C  
HETATM    5  C3  UNL     1      -3.281   1.602   1.024  1.00  0.00           C  
HETATM    6  N3  UNL     1      -2.537   2.148   2.002  1.00  0.00           N  
HETATM    7  C4  UNL     1      -1.402   1.478   2.109  1.00  0.00           C  
HETATM    8  N4  UNL     1      -1.395   0.477   1.189  1.00  0.00           N  
HETATM    9  C5  UNL     1      -0.283  -0.425   1.067  1.00  0.00           C  
HETATM   10  O1  UNL     1       0.949   0.261   0.997  1.00  0.00           O  
HETATM   11  C6  UNL     1       1.814  -0.785   0.714  1.00  0.00           C  
HETATM   12  C7  UNL     1       3.212  -0.323   0.395  1.00  0.00           C  
HETATM   13  O2  UNL     1       3.277   0.515  -0.700  1.00  0.00           O  
HETATM   14  P1  UNL     1       4.910   0.935  -0.913  1.00  0.00           P  
HETATM   15  O3  UNL     1       5.701  -0.250  -1.463  1.00  0.00           O  
HETATM   16  O4  UNL     1       5.077   2.254  -1.946  1.00  0.00           O  
HETATM   17  O5  UNL     1       5.619   1.330   0.572  1.00  0.00           O  
HETATM   18  C8  UNL     1       1.158  -1.437  -0.482  1.00  0.00           C  
HETATM   19  O6  UNL     1       1.530  -2.748  -0.662  1.00  0.00           O  
HETATM   20  C9  UNL     1      -0.329  -1.302  -0.125  1.00  0.00           C  
HETATM   21  O7  UNL     1      -0.760  -2.575   0.232  1.00  0.00           O  
HETATM   22  C10 UNL     1      -4.529   1.914   0.515  1.00  0.00           C  
HETATM   23  O8  UNL     1      -5.203   2.873   0.969  1.00  0.00           O  
HETATM   24  N5  UNL     1      -4.984   1.130  -0.499  1.00  0.00           N  
HETATM   25  H1  UNL     1      -4.563  -1.657  -2.190  1.00  0.00           H  
HETATM   26  H2  UNL     1      -5.500  -0.238  -2.694  1.00  0.00           H  
HETATM   27  H3  UNL     1      -0.624   1.721   2.830  1.00  0.00           H  
HETATM   28  H4  UNL     1      -0.227  -1.027   2.001  1.00  0.00           H  
HETATM   29  H5  UNL     1       1.855  -1.441   1.587  1.00  0.00           H  
HETATM   30  H6  UNL     1       3.810  -1.227   0.167  1.00  0.00           H  
HETATM   31  H7  UNL     1       3.623   0.165   1.300  1.00  0.00           H  
HETATM   32  H8  UNL     1       5.645   2.975  -1.571  1.00  0.00           H  
HETATM   33  H9  UNL     1       6.069   0.540   0.982  1.00  0.00           H  
HETATM   34  H10 UNL     1       1.406  -0.794  -1.367  1.00  0.00           H  
HETATM   35  H11 UNL     1       1.940  -3.099   0.148  1.00  0.00           H  
HETATM   36  H12 UNL     1      -0.819  -0.899  -1.007  1.00  0.00           H  
HETATM   37  H13 UNL     1      -0.583  -3.250  -0.472  1.00  0.00           H  
HETATM   38  H14 UNL     1      -5.926   1.359  -0.889  1.00  0.00           H  
CONECT    1    2   25   26
CONECT    2    3    3   24
CONECT    3    4
CONECT    4    5    5    8
CONECT    5    6   22
CONECT    6    7    7
CONECT    7    8   27
CONECT    8    9
CONECT    9   10   20   28
CONECT   10   11
CONECT   11   12   18   29
CONECT   12   13   30   31
CONECT   13   14
CONECT   14   15   15   16   17
CONECT   16   32
CONECT   17   33
CONECT   18   19   20   34
CONECT   19   35
CONECT   20   21   36
CONECT   21   37
CONECT   22   23   23   24
CONECT   24   38
END

HMDB0001397
     RDKit          3D
Guanosine monophosphate
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.8188   -0.6570   -2.0425 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2468    0.1029   -0.9763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0314   -0.1991   -0.4791 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5523    0.5514    0.5192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2813    1.6024    1.0237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5373    2.1485    2.0025 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4022    1.4782    2.1086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3955    0.4775    1.1895 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2830   -0.4247    1.0673 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9494    0.2612    0.9968 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8143   -0.7852    0.7138 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2122   -0.3230    0.3951 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2767    0.5149   -0.6995 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9100    0.9350   -0.9133 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.7008   -0.2504   -1.4633 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0768    2.2544   -1.9457 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6188    1.3295    0.5717 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1582   -1.4365   -0.4823 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5296   -2.7476   -0.6625 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3287   -1.3020   -0.1247 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7602   -2.5751    0.2323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5292    1.9140    0.5145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2034    2.8731    0.9691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9839    1.1298   -0.4993 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5625   -1.6572   -2.1905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4998   -0.2376   -2.6941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242    1.7215    2.8297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2274   -1.0266    2.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8553   -1.4414    1.5872 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8102   -1.2271    0.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6231    0.1647    1.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6455    2.9752   -1.5708 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0689    0.5395    0.9821 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4057   -0.7942   -1.3667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9402   -3.0991    0.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8188   -0.8986   -1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5833   -3.2499   -0.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9257    1.3589   -0.8891 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 14 17  1  0
 11 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
  5 22  1  0
 22 23  2  0
 22 24  1  0
 24  2  1  0
  8  4  1  0
 20  9  1  0
  1 25  1  0
  1 26  1  0
  7 27  1  0
  9 28  1  1
 11 29  1  1
 12 30  1  0
 12 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  6
 19 35  1  0
 20 36  1  6
 21 37  1  0
 24 38  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
5'-GMP	ChEBI
GMP	ChEBI
Guanosine 5'-phosphate	ChEBI
Guanosine-5'-monophosphate	ChEBI
Guanylic acid	ChEBI
pG	ChEBI
Guanosine 5'-monophosphate	Kegg
Guanosine 5'-phosphoric acid	Generator
Guanosine-5'-monophosphoric acid	Generator
Guanylate	Generator
Guanosine 5'-monophosphoric acid	Generator
Guanosine monophosphoric acid	Generator
e 626	HMDB
Guanidine monophosphate	HMDB
Guanosine 5'-phosphorate	HMDB
Guanosine-5'-phosphate	HMDB
Guanosine-phosphate	HMDB
5' Guanylic acid	HMDB
Acid, 5'-guanylic	HMDB
Acid, guanylic	HMDB
Guanosine 5' monophosphate	HMDB
5'-monoPhosphate, guanosine	HMDB
monoPhosphate, guanosine	HMDB
5'-Guanylic acid	HMDB

Chemical Formula

C₁₀H₁₄N₅O₈P

Average Molecular Weight

363.2206

Monoisotopic Molecular Weight

363.057998961

IUPAC Name

{[(2R,3S,4R,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

Traditional Name

guanylate

CAS Registry Number

85-32-5

SMILES

NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)C(=O)N1

InChI Identifier

InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1

InChI Key

RQFCJASXJCIDSX-UUOKFMHZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Sub Class

Purine ribonucleotides

Direct Parent

Purine ribonucleoside monophosphates

Alternative Parents

Substituents

Purine ribonucleoside monophosphate
Pentose phosphate
Pentose-5-phosphate
Glycosyl compound
N-glycosyl compound
6-oxopurine
Hypoxanthine
Monosaccharide phosphate
Pentose monosaccharide
Imidazopyrimidine
Purine
Aminopyrimidine
Monoalkyl phosphate
Pyrimidone
Alkyl phosphate
Pyrimidine
Monosaccharide
N-substituted imidazole
Organic phosphoric acid derivative
Phosphoric acid ester
Tetrahydrofuran
Azole
Imidazole
Heteroaromatic compound
Vinylogous amide
1,2-diol
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Primary amine
Organic nitrogen compound
Amine
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Alcohol
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

guanosine 5'-phosphate (CHEBI:17345 )
purine ribonucleoside 5'-monophosphate (CHEBI:17345 )
Ribonucleotides (C00144 )

Ontology

Physiological effect

Organoleptic effect

Odor

Odorless

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (HMDB: HMDB0001397)
Saliva (HMDB: HMDB0001397)

Organ

Tissue

Epithelium

Epidermis (HMDB: HMDB0001397)

Muscle tissue

Smooth muscle (HMDB: HMDB0001397)

Cell

Neuron (HMDB: HMDB0001397)

Hematocyte

Platelet (HMDB: HMDB0001397)

Cellular substructure

Extracellular (HMDB: HMDB0001397)

Organelle

Source

Exogenous

Exogenous (HMDB: HMDB0001397)

Food

Milk and milk product

Unfermented milk

Milk (Cow) (FooDB: FOOD00618)

Endogenous

Endogenous (HMDB: HMDB0001397)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Glutamate Metabolism (PathBank: SMP0087278)
Purine Nucleotides De Novo Biosynthesis 2 (PathBank: SMP0122223)
Purine Nucleotides De Novo Biosynthesis (PathBank: SMP0002377)
Purine Metabolism (PathBank: SMP0063668)
Purine Nucleotides De Novo Biosynthesis (PathBank: SMP0121307)
Guanine and Guanosine Salvage (PathBank: SMP0002086)

Disease pathway

4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency (PathBank: SMP0120445)
Xanthinuria Type II (PathBank: SMP0120578)
Succinic Semialdehyde Dehydrogenase Deficiency (PathBank: SMP0120631)
Gout or Kelley-Seegmiller Syndrome (PathBank: SMP0120709)
Xanthine Dehydrogenase Deficiency (Xanthinuria) (PathBank: SMP0120717)
Mitochondrial DNA Depletion Syndrome (PathBank: SMP0120820)
Adenylosuccinate Lyase Deficiency (PathBank: SMP0120670)
AICA-Ribosiduria (PathBank: SMP0120673)
Purine Nucleoside Phosphorylase Deficiency (PathBank: SMP0120756)
Adenine Phosphoribosyltransferase Deficiency (APRT) (PathBank: SMP0120819)
Myoadenylate Deaminase Deficiency (PathBank: SMP0120821)
Homocarnosinosis (PathBank: SMP0120494)
Lesch-Nyhan Syndrome (LNS) (PathBank: SMP0120508)
Adenosine Deaminase Deficiency (PathBank: SMP0120448)
2-Hydroxyglutric Aciduria (D and L Form) (PathBank: SMP0120659)
Molybdenum Cofactor Deficiency (PathBank: SMP0120752)
Hyperinsulinism-Hyperammonemia Syndrome (PathBank: SMP0120496)
Xanthinuria Type I (PathBank: SMP0120577)
Mitochondrial DNA Depletion Syndrome (PathBank: SMP0000536)

Drug action pathway

Methacycline Action Pathway (PathBank: SMP0000727)
Lincomycin Action Pathway (PathBank: SMP0000728)
Chloramphenicol Action Pathway (PathBank: SMP0000729)
Troleandomycin Action Pathway (PathBank: SMP0000730)
Josamycin Action Pathway (PathBank: SMP0000731)
Azathioprine Action Pathway (PathBank: SMP0000427)
Mercaptopurine Action Pathway (PathBank: SMP0000428)
Clomocycline Action Pathway (PathBank: SMP0000262)
Azithromycin Action Pathway (PathBank: SMP0000247)
Clarithromycin Action Pathway (PathBank: SMP0000248)
Clindamycin Action Pathway (PathBank: SMP0000249)
Erythromycin Action Pathway (PathBank: SMP0000250)
Roxithromycin Action Pathway (PathBank: SMP0000251)
Telithromycin Action Pathway (PathBank: SMP0000252)
Amikacin Action Pathway (PathBank: SMP0000253)
Gentamicin Action Pathway (PathBank: SMP0000254)
Kanamycin Action Pathway (PathBank: SMP0000255)
Neomycin Action Pathway (PathBank: SMP0000256)
Netilmicin Action Pathway (PathBank: SMP0000257)
Spectinomycin Action Pathway (PathBank: SMP0000258)
Streptomycin Action Pathway (PathBank: SMP0000259)
Demeclocycline Action Pathway (PathBank: SMP0000290)
Doxycycline Action Pathway (PathBank: SMP0000291)
Minocycline Action Pathway (PathBank: SMP0000292)
Oxytetracycline Action Pathway (PathBank: SMP0000293)
Tetracycline Action Pathway (PathBank: SMP0000294)
Lymecycline Action Pathway (PathBank: SMP0000295)
Thioguanine Action Pathway (PathBank: SMP0000430)
Tobramycin Action Pathway (PathBank: SMP0000711)
Tigecycline Action Pathway (PathBank: SMP0000712)
Arbekacin Action Pathway (PathBank: SMP0000713)
Paromomycin Action Pathway (PathBank: SMP0000714)
Rolitetracycline Action Pathway (PathBank: SMP0000726)

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	369 mg/mL	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct Type	Data Source	CCS Value (Å²)	Reference
[M-H]-	Not Available	170.4	http://allccs.zhulab.cn/database/detail?ID=AllCCS00000168
[M+H]+	Not Available	180.1	http://allccs.zhulab.cn/database/detail?ID=AllCCS00000168

Predicted Molecular Properties

Property	Value	Source
Water Solubility	3.56 g/L	ALOGPS
logP	-2	ALOGPS
logP	-3.1	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	1.29	ChemAxon
pKa (Strongest Basic)	0.38	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	201.75 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	75.49 m³·mol⁻¹	ChemAxon
Polarizability	30.7 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	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	180.391	31661259
DarkChem	[M-H]-	173.738	31661259
AllCCS	[M+H]+	176.976	32859911
AllCCS	[M-H]-	171.985	32859911
DeepCCS	[M+H]+	171.954	30932474
DeepCCS	[M-H]-	169.558	30932474
DeepCCS	[M-2H]-	203.465	30932474
DeepCCS	[M+Na]+	177.909	30932474
AllCCS	[M+H]+	177.0	32859911
AllCCS	[M+H-H2O]+	174.2	32859911
AllCCS	[M+NH4]+	179.6	32859911
AllCCS	[M+Na]+	180.3	32859911
AllCCS	[M-H]-	172.0	32859911
AllCCS	[M+Na-2H]-	171.6	32859911
AllCCS	[M+HCOO]-	171.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Guanosine monophosphate	NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)C(=O)N1	3886.4	Standard polar	33892256
Guanosine monophosphate	NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)C(=O)N1	2145.8	Standard non polar	33892256
Guanosine monophosphate	NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)C(=O)N1	3721.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Guanosine monophosphate,1TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	3117.3	Semi standard non polar	33892256
Guanosine monophosphate,1TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	3094.8	Semi standard non polar	33892256
Guanosine monophosphate,1TMS,isomer #3	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@H](O)[C@@H]1O	3248.6	Semi standard non polar	33892256
Guanosine monophosphate,1TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)[NH]1	3158.2	Semi standard non polar	33892256
Guanosine monophosphate,1TMS,isomer #5	C[Si](C)(C)N1C(N)=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C1=O	3156.6	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C	2983.9	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #10	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O	3211.2	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #11	C[Si](C)(C)N(C1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)[NH]1)[Si](C)(C)C	3102.3	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #12	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C	3151.2	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	3155.1	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #3	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)[NH]1	3018.6	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O	3070.4	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	3129.6	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	2997.8	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	3048.5	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #8	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3192.7	Semi standard non polar	33892256
Guanosine monophosphate,2TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)[NH]1	3170.1	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3058.0	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3211.7	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C	5003.5	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	3081.0	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	3289.1	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	4917.3	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	3109.7	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	3208.8	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	5184.3	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	3005.0	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	3471.4	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	5194.8	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #13	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3037.6	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #13	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3354.7	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #13	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	5285.9	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)[NH]1	3148.7	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)[NH]1	3287.1	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)[NH]1	4703.3	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #15	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3174.3	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #15	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3204.6	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #15	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	5024.0	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O	3133.7	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O	3417.4	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O	4873.3	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #17	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C	3181.6	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #17	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C	3313.4	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #17	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C	4962.9	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #18	C[Si](C)(C)N(C1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C)[Si](C)(C)C	3155.7	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #18	C[Si](C)(C)N(C1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C)[Si](C)(C)C	3505.3	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #18	C[Si](C)(C)N(C1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C)[Si](C)(C)C	5302.5	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	2956.8	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	3321.7	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	5255.4	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	2989.6	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3228.5	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	5512.4	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	3129.2	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	3204.9	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	4778.8	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)[NH]1	3090.8	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)[NH]1	3271.4	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)[NH]1	4890.0	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O	3131.0	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O	3188.1	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O	5154.6	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O	3025.7	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O	3456.3	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O	5172.3	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C	3056.2	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C	3333.5	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #8	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C	5264.4	Standard polar	33892256
Guanosine monophosphate,3TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	3109.2	Semi standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	3221.1	Standard non polar	33892256
Guanosine monophosphate,3TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	4813.6	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3074.1	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3121.7	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C	4645.9	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O	3100.3	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O	3423.4	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O	4843.3	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #11	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	3115.4	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #11	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	3212.5	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #11	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	4388.2	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	3141.3	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	3123.1	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	4783.8	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #13	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	3106.4	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #13	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	3357.7	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #13	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	4536.1	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3143.0	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3235.7	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	4632.8	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	3082.7	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	3444.5	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	4863.7	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #16	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3164.7	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #16	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3340.3	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #16	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	4332.0	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #17	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C	3203.5	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #17	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C	3217.6	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #17	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C	4424.4	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #18	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O	3217.3	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #18	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O	3387.9	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #18	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O	4610.5	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	3075.0	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	3212.3	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	4617.2	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3100.1	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3132.2	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	4983.9	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3016.3	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3398.9	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C	4797.7	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3032.0	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3274.4	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	4906.9	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)[NH]1	3121.1	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)[NH]1	3185.1	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)[NH]1	4348.0	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O	3162.0	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O	3103.0	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O	4746.8	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O	3119.5	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O	3338.0	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O	4510.7	Standard polar	33892256
Guanosine monophosphate,4TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C	3156.7	Semi standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C	3213.3	Standard non polar	33892256
Guanosine monophosphate,4TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C	4607.3	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	3133.3	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	3138.5	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)[NH]1	4133.3	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3201.8	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3144.5	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	4142.2	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	3181.4	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	3333.1	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	4263.5	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3250.1	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3298.5	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C	4111.1	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3145.6	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3048.0	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	4635.3	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3128.8	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3296.4	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C	4214.2	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3151.7	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3165.9	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	4326.3	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3093.2	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3378.3	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	4463.6	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O	3172.7	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O	3253.9	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O	4001.4	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #7	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C	3212.0	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #7	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C	3121.3	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #7	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C	4101.5	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O	3196.2	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O	3311.8	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O	4238.8	Standard polar	33892256
Guanosine monophosphate,5TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	3164.0	Semi standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	3281.2	Standard non polar	33892256
Guanosine monophosphate,5TMS,isomer #9	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	4040.6	Standard polar	33892256
Guanosine monophosphate,6TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3203.9	Semi standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3203.0	Standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C	3836.0	Standard polar	33892256
Guanosine monophosphate,6TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3230.4	Semi standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3086.2	Standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3918.8	Standard polar	33892256
Guanosine monophosphate,6TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3215.6	Semi standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3270.3	Standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3989.3	Standard polar	33892256
Guanosine monophosphate,6TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O	3273.7	Semi standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O	3219.2	Standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O	3820.2	Standard polar	33892256
Guanosine monophosphate,6TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	3260.9	Semi standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	3246.8	Standard non polar	33892256
Guanosine monophosphate,6TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	3856.9	Standard polar	33892256
Guanosine monophosphate,7TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3313.6	Semi standard non polar	33892256
Guanosine monophosphate,7TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3188.6	Standard non polar	33892256
Guanosine monophosphate,7TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C	3694.4	Standard polar	33892256
Guanosine monophosphate,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	3360.8	Semi standard non polar	33892256
Guanosine monophosphate,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	3339.7	Semi standard non polar	33892256
Guanosine monophosphate,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@H](O)[C@@H]1O	3463.2	Semi standard non polar	33892256
Guanosine monophosphate,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)[NH]1	3350.7	Semi standard non polar	33892256
Guanosine monophosphate,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N1C(N)=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C1=O	3389.7	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3459.5	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]1O	3616.7	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)[NH]1)[Si](C)(C)C(C)(C)C	3499.9	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	3553.9	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	3563.5	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)[NH]1	3440.5	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	3533.7	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	3543.5	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3423.8	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	3510.6	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3590.3	Semi standard non polar	33892256
Guanosine monophosphate,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)[NH]1	3558.2	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3656.6	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3723.8	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	5048.2	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3687.2	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3825.5	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	4933.8	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	3753.0	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	3759.9	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	5175.0	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	3612.7	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	3994.9	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	5067.7	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3680.8	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3900.0	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	5132.1	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)[NH]1	3733.5	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)[NH]1	3745.4	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)[NH]1	4779.8	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3791.1	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3685.8	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	5034.0	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O	3707.7	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O	3909.0	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O	4859.1	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	3793.4	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	3810.6	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	4917.0	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3747.7	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4006.4	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5113.9	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3566.5	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3887.0	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	5166.1	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3680.9	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3794.5	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	5439.0	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	3696.9	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	3651.5	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O	4854.3	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)[NH]1	3694.0	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)[NH]1	3796.4	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)[NH]1	4910.2	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	3771.0	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	3732.0	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	5144.0	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@@H]1O	3624.1	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@@H]1O	3973.6	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@@H]1O	5049.4	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	3697.6	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	3874.1	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	5113.4	Standard polar	33892256
Guanosine monophosphate,3TBDMS,isomer #9	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)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	3676.3	Semi standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #9	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)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	3680.6	Standard non polar	33892256
Guanosine monophosphate,3TBDMS,isomer #9	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)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=O	4890.5	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3836.1	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3712.5	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	4729.6	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	3907.4	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	4079.4	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	4742.4	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3887.0	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3864.0	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	4544.0	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #12	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)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	3940.0	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #12	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)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	3759.5	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #12	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)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O	4836.9	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	3862.8	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	4028.9	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	4549.4	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3952.8	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3921.6	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	4633.5	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O	3897.8	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O	4106.7	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O	4758.6	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3877.9	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3941.1	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	4451.7	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	3967.7	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	3828.3	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	4523.2	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]1O	3957.5	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]1O	4016.5	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)[C@H](O)[C@@H]1O	4610.6	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3854.6	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3911.5	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	4679.0	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3938.9	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3812.4	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	4976.0	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	3785.6	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	4072.6	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@@H]1O[Si](C)(C)C(C)(C)C	4721.3	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3847.8	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3971.6	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	4813.1	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)[NH]1	3893.2	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)[NH]1	3825.4	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)[NH]1	4508.6	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	3954.0	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	3728.3	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)[C@@H]1O	4801.5	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@@H]1O	3872.9	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@@H]1O	3998.0	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)[C@@H]1O	4528.1	Standard polar	33892256
Guanosine monophosphate,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	3962.4	Semi standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	3887.1	Standard non polar	33892256
Guanosine monophosphate,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(=O)N1[Si](C)(C)C(C)(C)C	4611.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental GC-MS	GC-MS Spectrum - Guanosine monophosphate GC-MS (6 TMS)	splash10-014i-1942000000-27fc2e135f86071ba4d7	2014-06-16	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Guanosine monophosphate GC-MS (Non-derivatized)	splash10-014i-1942000000-27fc2e135f86071ba4d7	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Guanosine monophosphate GC-EI-TOF (Non-derivatized)	splash10-014i-0941000000-245c5258141d8d2a9fa5	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Guanosine monophosphate GC-MS (Non-derivatized) - 70eV, Positive	splash10-0002-9722000000-9155df338c7516c297b6	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Guanosine monophosphate GC-MS (2 TMS) - 70eV, Positive	splash10-01ot-9522200000-3e2591b21841c753ec13	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Guanosine monophosphate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate Quattro_QQQ 10V, Positive-QTOF (Annotated)	splash10-0udi-0901000000-fbce35f7dfa73ab5fc11	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate Quattro_QQQ 25V, Positive-QTOF (Annotated)	splash10-0udi-0900000000-764722cc1b8cc2aaa480	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate Quattro_QQQ 40V, Positive-QTOF (Annotated)	splash10-0udi-0900000000-c268cdce8dfd6c39fa3c	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) , Positive-QTOF	splash10-03di-0409000000-309e438ad8b6162df850	2012-08-31	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) 30V, Positive-QTOF	splash10-0udi-0904000000-cf72d0459316801b014e	2012-08-31	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) , Positive-QTOF	splash10-0udi-0900000000-abc7bfe7620db1c34775	2012-08-31	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) , Negative-QTOF	splash10-01t9-9114000000-9a1071a2e17ea3ca268c	2012-08-31	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) , Negative-QTOF	splash10-01t9-9113000000-05a8989070e3b89138f1	2012-08-31	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF , negative-QTOF	splash10-01t9-9114000000-9a1071a2e17ea3ca268c	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF , negative-QTOF	splash10-01t9-9113000000-05a8989070e3b89138f1	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF , positive-QTOF	splash10-03di-0409000000-309e438ad8b6162df850	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF , positive-QTOF	splash10-0udi-0904000000-cf72d0459316801b014e	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate LC-ESI-QTOF , positive-QTOF	splash10-0udi-0900000000-abc7bfe7620db1c34775	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate 40V, Negative-QTOF	splash10-004i-9000000000-c340c748805ec82deb0d	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate 10V, Negative-QTOF	splash10-03di-3009000000-5d594db970a4fea1099e	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate 20V, Negative-QTOF	splash10-004i-9011000000-8335076473133728e58f	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate 30V, Positive-QTOF	splash10-0udi-0904000000-cf72d0459316801b014e	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate 20V, Positive-QTOF	splash10-0udi-0900000000-1f479e6ff94baf0265bc	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Guanosine monophosphate 40V, Positive-QTOF	splash10-0udi-1900000000-1dd27aac9ee9a0882191	2021-09-20	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Guanosine monophosphate 10V, Positive-QTOF	splash10-0udi-0913000000-05cd931f142e4b624c8b	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Guanosine monophosphate 20V, Positive-QTOF	splash10-0udi-0900000000-318d089a94a5bcfd20f2	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Guanosine monophosphate 40V, Positive-QTOF	splash10-0udi-0900000000-e616291ba80c4abf405c	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Guanosine monophosphate 10V, Negative-QTOF	splash10-0imi-7709000000-6c811759b6f078f642a2	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Guanosine monophosphate 20V, Negative-QTOF	splash10-0fb9-9800000000-59c4ae8bf5bfa0d23da1	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Guanosine monophosphate 40V, Negative-QTOF	splash10-004i-9100000000-73f60c52b80206170819	2016-09-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Experimental 1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, experimental)	2012-12-04	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Experimental 2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, H₂O, experimental)	2012-12-05	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Mitochondria
Nucleus
Lysosome
Golgi apparatus

Biospecimen Locations

Blood
Saliva

Tissue Locations

Bladder
Epidermis
Heart
Intestine
Neuron
Platelet
Smooth Muscle

Pathways

Name	SMPDB/PathBank	KEGG
Transcription/Translation	SMP00019	Not Available
Purine metabolism	Not Available
Glutamate Metabolism
Adenosine Deaminase Deficiency		Not Available
Adenylosuccinate Lyase Deficiency		Not Available

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	0.0099 +/- 0.0024 uM	Adult (>18 years old)	Male	Normal	Geigy Scientific ...	details
Blood	Detected and Quantified	0.0095 +/- 0.0021 uM	Adult (>18 years old)	Female	Normal	Geigy Scientific ...	details
Saliva	Detected and Quantified	0.0898 +/- 0.212 uM	Adult (>18 years old)	Female	Normal	Sugimoto et al. (...	details
Saliva	Detected and Quantified	0.199 +/- 0.245 uM	Adult (>18 years old)	Both	Normal	Sugimoto et al. (...	details
Saliva	Detected and Quantified	0.262 +/- 0.501 uM	Adult (>18 years old)	Female	Normal	Sugimoto et al. (...	details
Saliva	Detected and Quantified	0.312 +/- 0.229 uM	Adult (>18 years old)	Both	Normal	Sugimoto et al. (...	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

DB01972

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Wikipedia Link

Guanosine_monophosphate

METLIN ID

6216

PubChem Compound

6804

PDB ID

Not Available

ChEBI ID

17345

Food Biomarker Ontology

Not Available

VMH ID

GMP

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Sato, Katsuaki; Matsui, Hiroshi; Ei, Hitoshi; Takinami, Koichi. Guanosine-5'-monophosphate. Jpn. Kokai Tokkyo Koho (1979), 3 pp.

Material Safety Data Sheet (MSDS)

Not Available

General References

Scheen AJ: [Medication of the month. Vardenafil (Levitra)]. Rev Med Liege. 2003 Sep;58(9):576-9. [PubMed:14626653 ]
Begonja AJ, Gambaryan S, Geiger J, Aktas B, Pozgajova M, Nieswandt B, Walter U: Platelet NAD(P)H-oxidase-generated ROS production regulates alphaIIbbeta3-integrin activation independent of the NO/cGMP pathway. Blood. 2005 Oct 15;106(8):2757-60. Epub 2005 Jun 23. [PubMed:15976180 ]
Zhao L, Gray L, Leonardi-Bee J, Weaver CS, Heptinstall S, Bath PM: Effect of aspirin, clopidogrel and dipyridamole on soluble markers of vascular function in normal volunteers and patients with prior ischaemic stroke. Platelets. 2006 Mar;17(2):100-4. [PubMed:16421011 ]
Matata BM, Galinanes M: Effect of diabetes on nitric oxide metabolism during cardiac surgery. Diabetes. 2001 Nov;50(11):2603-10. [PubMed:11679441 ]
Sales ME, Espanol AJ, Sterin-Borda L, Borda E, de Bracco MM: Protein kinase C regulates NO-cGMP pathway in muscarinic receptor activation by HIV+-IgA. Int J Mol Med. 1999 Jun;3(6):633-7. [PubMed:10341295 ]
Boehning D, Moon C, Sharma S, Hurt KJ, Hester LD, Ronnett GV, Shugar D, Snyder SH: Carbon monoxide neurotransmission activated by CK2 phosphorylation of heme oxygenase-2. Neuron. 2003 Sep 25;40(1):129-37. [PubMed:14527438 ]
Favory R, Lancel S, Tissier S, Mathieu D, Decoster B, Neviere R: Myocardial dysfunction and potential cardiac hypoxia in rats induced by carbon monoxide inhalation. Am J Respir Crit Care Med. 2006 Aug 1;174(3):320-5. Epub 2006 May 11. [PubMed:16690979 ]
Yildiz O, Gul H, Ozgok Y, Onguru O, Kilciler M, Aydin A, Isimer A, Harmankaya AC: Increased vasoconstrictor reactivity and decreased endothelial function in high grade varicocele; functional and morphological study. Urol Res. 2003 Oct;31(5):323-8. Epub 2003 Jul 11. [PubMed:14574537 ]
Seftel AD: Phosphodiesterase type 5 inhibitor differentiation based on selectivity, pharmacokinetic, and efficacy profiles. Clin Cardiol. 2004 Apr;27(4 Suppl 1):I14-19. [PubMed:15115191 ]
Salomon P, Przewlocka-Kosmala M, Orda A: [Plasma levels of brain natriuretic peptide, cyclic 3'5'-guanosine monophosphate, endothelin 1, and noradrenaline in patients with chronic congestive heart failure]. Pol Arch Med Wewn. 2003 Jan;109(1):43-8. [PubMed:12879765 ]
Khush KK, De Marco T, Vakharia KT, Harmon C, Fineman JR, Chatterjee K, Michaels AD: Nesiritide acutely increases pulmonary and systemic levels of nitric oxide in patients with pulmonary hypertension. J Card Fail. 2006 Sep;12(7):507-13. [PubMed:16952783 ]
Yoshimura N, Seki S, Chancellor MB, de Groat WC, Ueda T: Targeting afferent hyperexcitability for therapy of the painful bladder syndrome. Urology. 2002 May;59(5 Suppl 1):61-7. [PubMed:12007524 ]
Ralph DJ: Normal erectile function. Clin Cornerstone. 2005;7(1):13-8. [PubMed:16156419 ]
Rosen RC, McKenna KE: PDE-5 inhibition and sexual response: pharmacological mechanisms and clinical outcomes. Annu Rev Sex Res. 2002;13:36-88. [PubMed:12836729 ]
Zusman RM, Morales A, Glasser DB, Osterloh IH: Overall cardiovascular profile of sildenafil citrate. Am J Cardiol. 1999 Mar 4;83(5A):35C-44C. [PubMed:10078541 ]
Hamed EA, Meki AR, Gaafar AA, Hamed SA: Role of some vasoactive mediators in patients with erectile dysfunction: their relationship with angiotensin-converting enzyme and growth hormone. Int J Impot Res. 2003 Dec;15(6):418-25. [PubMed:14671660 ]
Ehsan A, Sommer F, Schmidt A, Klotz T, Koslowski J, Niggemann S, Jacobs G, Engelmann U, Addicks K, Bloch W: Nitric oxide pathways in human bladder carcinoma. The distribution of nitric oxide synthases, soluble guanylyl cyclase, cyclic guanosine monophosphate, and nitrotyrosine. Cancer. 2002 Dec 1;95(11):2293-301. [PubMed:12436434 ]
Lepore JJ, Maroo A, Bigatello LM, Dec GW, Zapol WM, Bloch KD, Semigran MJ: Hemodynamic effects of sildenafil in patients with congestive heart failure and pulmonary hypertension: combined administration with inhaled nitric oxide. Chest. 2005 May;127(5):1647-53. [PubMed:15888841 ]
Kekilli M, Beyazit Y, Purnak T, Dogan S, Atalar E: Acute myocardial infarction after sildenafil citrate ingestion. Ann Pharmacother. 2005 Jul-Aug;39(7-8):1362-4. Epub 2005 May 24. [PubMed:15914518 ]
Ivanovic Z, Duchez P, Dazey B, Hermitte F, Lamrissi-Garcia I, Mazurier F, Praloran V, Reiffers J, Vezon G, Boiron JM: A clinical-scale expansion of mobilized CD 34+ hematopoietic stem and progenitor cells by use of a new serum-free medium. Transfusion. 2006 Jan;46(1):126-31. [PubMed:16398741 ]

Only showing the first 10 proteins. There are 198 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details

1. 5'-nucleotidase

General function:: Involved in hydrolase activity
Specific function:: Hydrolyzes extracellular nucleotides into membrane permeable nucleosides.
Gene Name:: NT5E
Uniprot ID:: P21589
Molecular weight:: 57948.125

Reactions

Guanosine monophosphate + Water → Guanosine + Phosphate	details

Enzyme Details

2. Cytosolic 5'-nucleotidase 1B

General function:: Involved in nucleotide binding
Specific function:: Dephosphorylates the 5' and 2'(3')-phosphates of deoxyribonucleotides. Helps to regulate adenosine levels (By similarity).
Gene Name:: NT5C1B
Uniprot ID:: Q96P26
Molecular weight:: 68803.055

Reactions

Guanosine monophosphate + Water → Guanosine + Phosphate	details

Enzyme Details

3. Cytosolic 5'-nucleotidase 1A

General function:: Involved in nucleotide binding
Specific function:: Dephosphorylates the 5' and 2'(3')-phosphates of deoxyribonucleotides and has a broad substrate specificity. Helps to regulate adenosine levels in heart during ischemia and hypoxia.
Gene Name:: NT5C1A
Uniprot ID:: Q9BXI3
Molecular weight:: 41020.145

Reactions

Guanosine monophosphate + Water → Guanosine + Phosphate	details

Enzyme Details

4. 5'(3')-deoxyribonucleotidase, cytosolic type

General function:: Involved in metal ion binding
Specific function:: Dephosphorylates the 5' and 2'(3')-phosphates of deoxyribonucleotides, with a preference for dUMP and dTMP, intermediate activity towards dGMP, and low activity towards dCMP and dAMP.
Gene Name:: NT5C
Uniprot ID:: Q8TCD5
Molecular weight:: Not Available

Reactions

Guanosine monophosphate + Water → Guanosine + Phosphate	details

Enzyme Details

5. 5'(3')-deoxyribonucleotidase, mitochondrial

General function:: Involved in phosphatase activity
Specific function:: Dephosphorylates specifically the 5' and 2'(3')-phosphates of uracil and thymine deoxyribonucleotides, and so protects mitochondrial DNA replication from excess dTTP. Has only marginal activity towards dIMP and dGMP.
Gene Name:: NT5M
Uniprot ID:: Q9NPB1
Molecular weight:: Not Available

Reactions

Guanosine monophosphate + Water → Guanosine + Phosphate	details

Enzyme Details

6. Ectonucleoside triphosphate diphosphohydrolase 1

General function:: Involved in hydrolase activity
Specific function:: In the nervous system, could hydrolyze ATP and other nucleotides to regulate purinergic neurotransmission. Could also be implicated in the prevention of platelet aggregation by hydrolyzing platelet-activating ADP to AMP. Hydrolyzes ATP and ADP equally well.
Gene Name:: ENTPD1
Uniprot ID:: P49961
Molecular weight:: 58706.0

Reactions

Guanosine diphosphate + Water → Guanosine monophosphate + Phosphate	details

Enzyme Details

7. Soluble calcium-activated nucleotidase 1

General function:: Involved in calcium ion binding
Specific function:: Calcium-dependent nucleotidase with a preference for UDP. The order of activity with different substrates is UDP > GDP > UTP > GTP. Has very low activity towards ADP and even lower activity towards ATP. Does not hydrolyze AMP and GMP. Involved in proteoglycan synthesis.
Gene Name:: CANT1
Uniprot ID:: Q8WVQ1
Molecular weight:: 44839.24

Reactions

Guanosine diphosphate + Water → Guanosine monophosphate + Phosphate	details

Enzyme Details

8. Ectonucleoside triphosphate diphosphohydrolase 3

General function:: Involved in hydrolase activity
Specific function:: Has a threefold preference for the hydrolysis of ATP over ADP.
Gene Name:: ENTPD3
Uniprot ID:: O75355
Molecular weight:: 59104.76

Reactions

Guanosine diphosphate + Water → Guanosine monophosphate + Phosphate	details

Enzyme Details

9. Inosine triphosphate pyrophosphatase

General function:: Involved in hydrolase activity
Specific function:: Pyrophosphatase that hydrolyzes the non-canonical purine nucleotides inosine triphosphate (ITP), deoxyinosine triphosphate (dITP) as well as 2'-deoxy-N-6-hydroxylaminopurine triposphate (dHAPTP) and xanthosine 5'-triphosphate (XTP) to their respective monophosphate derivatives. The enzyme does not distinguish between the deoxy- and ribose forms. Probably excludes non-canonical purines from RNA and DNA precursor pools, thus preventing their incorporation into RNA and DNA and avoiding chromosomal lesions.
Gene Name:: ITPA
Uniprot ID:: Q9BY32
Molecular weight:: 16833.23

Reactions

Guanosine triphosphate + Water → Guanosine monophosphate + Pyrophosphate	details

Enzyme Details

10. Adenine phosphoribosyltransferase

General function:: Involved in adenine phosphoribosyltransferase activity
Specific function:: Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis.
Gene Name:: APRT
Uniprot ID:: P07741
Molecular weight:: 19607.535

Reactions

Guanosine monophosphate + Pyrophosphate → Guanine + Phosphoribosyl pyrophosphate	details

Only showing the first 10 proteins. There are 198 proteins in total.

Show all enzymes and transporters

Showing metabocard for Guanosine monophosphate (HMDB0001397)

MOL for HMDB0001397 (Guanosine monophosphate)

3D MOL for HMDB0001397 (Guanosine monophosphate)

3D SDF for HMDB0001397 (Guanosine monophosphate)

3D-SDF for HMDB0001397 (Guanosine monophosphate)

PDB for HMDB0001397 (Guanosine monophosphate)

3D PDB for HMDB0001397 (Guanosine monophosphate)

SMILES for HMDB0001397 (Guanosine monophosphate)

INCHI for HMDB0001397 (Guanosine monophosphate)

Structure for HMDB0001397 (Guanosine monophosphate)

3D Structure for HMDB0001397 (Guanosine monophosphate)

Experimental Collision Cross Sections

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

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