Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (3) Show 3 proteins XML

Show more...Show more...Show more...

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2013-05-17 01:01:02 UTC

Update Date

2021-09-14 14:58:17 UTC

HMDB ID

HMDB0060415

Secondary Accession Numbers

HMDB60415

Metabolite Identification

Common Name

6-Thioguanosine monophosphate

Description

6-Thioguanosine monophosphate, also known as 6-TG nucleotide, 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. 6-Thioguanosine monophosphate is a metabolite of tioguanine. 6-Thioguanosine monophosphate is a strong basic compound (based on its pKa). 6-Thioguanosine monophosphate exists in all living organisms, ranging from bacteria to humans. 6-thioguanosine monophosphate and pyrophosphate can be biosynthesized from thioguanine and phosphoribosyl pyrophosphate; which is catalyzed by the enzyme hypoxanthine-guanine phosphoribosyltransferase. It is a guanine analog. In humans, 6-thioguanosine monophosphate is involved in thioguanine metabolism pathway. Tioguanine, formerly thioguanine, is a drug that is used in the treatment of cancer.

Structure

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

HMDB0060415
     RDKit          3D
6-Thioguanosine monophosphate
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.2270    1.9531   -1.9416 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0211    0.9503   -0.9127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0874    0.3375   -0.3046 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0155   -0.5530    0.6882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2770   -1.3625    1.3172 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7096   -0.8302    1.0933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2452   -1.6840    2.0348 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9042   -1.6410    2.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5546   -0.7417    1.0433 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1612   -0.5729    0.6687 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3652    0.5936    0.3210 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6150    0.1999   -0.0623 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7033    1.0703   -0.5044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413    1.9330    0.5746 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7456    1.8204    0.7594 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.8964    1.5543    2.2721 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6511    3.0602    0.2346 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2617    0.3565   -0.0123 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4485   -1.0180   -0.9337 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2493   -2.0612   -0.4520 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0151   -1.3318   -0.6981 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3606   -2.6563   -0.5759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6265   -0.2557    0.5181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7808    0.6359   -0.4860 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1353    2.9461   -1.6582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4366    1.7326   -2.9388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3104   -2.2343    2.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5337   -1.1107    1.3431 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0130   -0.2572    0.9907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3137    1.7902   -1.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5709    0.5713   -0.8982 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5823    3.4076   -0.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7499   -0.3814    0.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6928   -0.7947   -1.9892 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7177   -2.7476   -0.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5926   -0.7708   -1.4667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7181   -3.0211   -1.3975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9724    1.1134   -0.9278 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
  4  6  1  0
  6  7  1  0
  7  8  2  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  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 12 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
  9 23  1  0
 23 24  1  0
 24  2  1  0
 23  6  2  0
 21 10  1  0
  1 25  1  0
  1 26  1  0
  8 27  1  0
 10 28  1  1
 12 29  1  1
 13 30  1  0
 13 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  6
 20 35  1  0
 21 36  1  6
 22 37  1  0
 24 38  1  0
M  END

  Mrv0541 09061309122D          

 24 26  0  0  0  0            999 V2000
   -1.8505   -3.7149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -3.2299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -3.4849    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0865   -2.8174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -2.1500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -4.2695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9115   -2.8174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9391   -4.3492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7565   -3.1968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7867   -4.5317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6042   -3.3793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -2.4049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2716   -3.8642    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  1  0  0  0
  5  3  1  0  0  0  0
  6  5  1  0  0  0  0
  7  4  2  0  0  0  0
  8  4  1  0  0  0  0
  9  6  1  0  0  0  0
 11 10  1  0  0  0  0
 12  2  2  0  0  0  0
 12  4  1  0  0  0  0
 13  7  1  0  0  0  0
 13 10  1  0  0  0  0
 14  8  1  0  0  0  0
 14 10  2  0  0  0  0
 15  2  1  0  0  0  0
 15  7  1  0  0  0  0
  9 15  1  1  0  0  0
  5 16  1  6  0  0  0
  6 17  1  6  0  0  0
 21  1  1  0  0  0  0
 22  3  1  0  0  0  0
 22  9  1  0  0  0  0
 23 18  1  0  0  0  0
 23 19  1  0  0  0  0
 23 20  2  0  0  0  0
 23 21  1  0  0  0  0
 24  8  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0060415

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=NC(=S)C2=C(N1)N(C=N2)[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C10H14N5O7PS/c11-10-13-7-4(8(24)14-10)12-2-15(7)9-6(17)5(16)3(22-9)1-21-23(18,19)20/h2-3,5-6,9,16-17H,1H2,(H2,18,19,20)(H3,11,13,14,24)/t3-,5-,6-,9-/m1/s1

> <INCHI_KEY>
BPZXYEUJBFHASJ-UUOKFMHZSA-N

> <FORMULA>
C10H14N5O7PS

> <MOLECULAR_WEIGHT>
379.286

> <EXACT_MASS>
379.035155029

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
33.25060305088701

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-1.39

> <JCHEM_LOGP>
-3.6099075506501905

> <ALOGPS_LOGS>
-2.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.250553716622566

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2313432649868896

> <JCHEM_PKA_STRONGEST_BASIC>
3.3934808641244985

> <JCHEM_POLAR_SURFACE_AREA>
184.67999999999995

> <JCHEM_REFRACTIVITY>
83.05149999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.81e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4R,5R)-5-(2-amino-6-sulfanylidene-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060415
     RDKit          3D
6-Thioguanosine monophosphate
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.2270    1.9531   -1.9416 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0211    0.9503   -0.9127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0874    0.3375   -0.3046 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0155   -0.5530    0.6882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2770   -1.3625    1.3172 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7096   -0.8302    1.0933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2452   -1.6840    2.0348 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9042   -1.6410    2.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5546   -0.7417    1.0433 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1612   -0.5729    0.6687 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3652    0.5936    0.3210 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6150    0.1999   -0.0623 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7033    1.0703   -0.5044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413    1.9330    0.5746 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7456    1.8204    0.7594 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.8964    1.5543    2.2721 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6511    3.0602    0.2346 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2617    0.3565   -0.0123 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4485   -1.0180   -0.9337 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2493   -2.0612   -0.4520 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0151   -1.3318   -0.6981 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3606   -2.6563   -0.5759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6265   -0.2557    0.5181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7808    0.6359   -0.4860 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1353    2.9461   -1.6582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4366    1.7326   -2.9388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3104   -2.2343    2.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5337   -1.1107    1.3431 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0130   -0.2572    0.9907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3137    1.7902   -1.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5709    0.5713   -0.8982 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5823    3.4076   -0.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7499   -0.3814    0.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6928   -0.7947   -1.9892 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7177   -2.7476   -0.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5926   -0.7708   -1.4667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7181   -3.0211   -1.3975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9724    1.1134   -0.9278 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
  4  6  1  0
  6  7  1  0
  7  8  2  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  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 12 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
  9 23  1  0
 23 24  1  0
 24  2  1  0
 23  6  2  0
 21 10  1  0
  1 25  1  0
  1 26  1  0
  8 27  1  0
 10 28  1  1
 12 29  1  1
 13 30  1  0
 13 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  6
 20 35  1  0
 21 36  1  6
 22 37  1  0
 24 38  1  0
M  END

HEADER    PROTEIN                                 06-SEP-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-13         0                                  
HETATM    1  C   UNK     0      -3.454  -6.934   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.208  -6.029   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.744  -6.505   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.161  -5.259   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.530   0.237   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.744  -4.013   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.864  -2.073   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       5.198  -2.843   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0      -0.268  -0.057   0.000  0.00  0.00           N+0
HETATM   13  N   UNK     0       2.530  -2.843   0.000  0.00  0.00           N+0
HETATM   14  N   UNK     0       3.864  -0.533   0.000  0.00  0.00           N+0
HETATM   15  N   UNK     0      -0.268  -2.549   0.000  0.00  0.00           N+0
HETATM   16  O   UNK     0      -0.268  -7.970   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       1.701  -5.259   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -7.353  -8.119   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -7.012  -5.967   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -5.202  -8.459   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -4.861  -6.308   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -2.208  -4.489   0.000  0.00  0.00           O+0
HETATM   23  P   UNK     0      -6.107  -7.213   0.000  0.00  0.00           P+0
HETATM   24  S   UNK     0       2.530   1.777   0.000  0.00  0.00           S+0
CONECT    1    3   21                                                       
CONECT    2   12   15                                                       
CONECT    3    1    5   22                                                  
CONECT    4    7    8   12                                                  
CONECT    5    3    6   16                                                  
CONECT    6    5    9   17                                                  
CONECT    7    4   13   15                                                  
CONECT    8    4   14   24                                                  
CONECT    9    6   15   22                                                  
CONECT   10   11   13   14                                                  
CONECT   11   10                                                            
CONECT   12    2    4                                                       
CONECT   13    7   10                                                       
CONECT   14    8   10                                                       
CONECT   15    2    7    9                                                  
CONECT   16    5                                                            
CONECT   17    6                                                            
CONECT   18   23                                                            
CONECT   19   23                                                            
CONECT   20   23                                                            
CONECT   21    1   23                                                       
CONECT   22    3    9                                                       
CONECT   23   18   19   20   21                                             
CONECT   24    8                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

COMPND    HMDB0060789
HETATM    1  N1  UNL     1      -5.409   2.453   0.648  1.00  0.00           N  
HETATM    2  C1  UNL     1      -4.818   1.211   0.229  1.00  0.00           C  
HETATM    3  N2  UNL     1      -5.600   0.156  -0.107  1.00  0.00           N  
HETATM    4  C2  UNL     1      -5.076  -1.019  -0.503  1.00  0.00           C  
HETATM    5  S1  UNL     1      -6.012  -2.299  -0.912  1.00  0.00           S  
HETATM    6  C3  UNL     1      -3.698  -1.096  -0.551  1.00  0.00           C  
HETATM    7  N3  UNL     1      -2.880  -2.096  -0.894  1.00  0.00           N  
HETATM    8  C4  UNL     1      -1.604  -1.660  -0.770  1.00  0.00           C  
HETATM    9  N4  UNL     1      -1.587  -0.389  -0.351  1.00  0.00           N  
HETATM   10  C5  UNL     1      -0.452   0.485  -0.080  1.00  0.00           C  
HETATM   11  O1  UNL     1       0.578   0.182  -0.933  1.00  0.00           O  
HETATM   12  C6  UNL     1       1.750   0.317  -0.212  1.00  0.00           C  
HETATM   13  C7  UNL     1       2.938  -0.298  -0.884  1.00  0.00           C  
HETATM   14  O2  UNL     1       4.048  -0.096  -0.064  1.00  0.00           O  
HETATM   15  P1  UNL     1       5.449  -0.757  -0.738  1.00  0.00           P  
HETATM   16  O3  UNL     1       5.314  -0.965  -2.224  1.00  0.00           O  
HETATM   17  O4  UNL     1       6.728   0.293  -0.404  1.00  0.00           O  
HETATM   18  O5  UNL     1       5.765  -2.231  -0.005  1.00  0.00           O  
HETATM   19  C8  UNL     1       1.385  -0.399   1.079  1.00  0.00           C  
HETATM   20  O6  UNL     1       2.290  -0.153   2.086  1.00  0.00           O  
HETATM   21  C9  UNL     1       0.048   0.314   1.336  1.00  0.00           C  
HETATM   22  O7  UNL     1       0.377   1.564   1.847  1.00  0.00           O  
HETATM   23  C10 UNL     1      -2.877  -0.030  -0.212  1.00  0.00           C  
HETATM   24  N5  UNL     1      -3.487   1.116   0.177  1.00  0.00           N  
HETATM   25  H1  UNL     1      -5.939   3.007  -0.039  1.00  0.00           H  
HETATM   26  H2  UNL     1      -5.311   2.792   1.616  1.00  0.00           H  
HETATM   27  H3  UNL     1      -0.679  -2.213  -0.967  1.00  0.00           H  
HETATM   28  H4  UNL     1      -0.774   1.527  -0.287  1.00  0.00           H  
HETATM   29  H5  UNL     1       1.959   1.367   0.004  1.00  0.00           H  
HETATM   30  H6  UNL     1       2.795  -1.371  -1.118  1.00  0.00           H  
HETATM   31  H7  UNL     1       3.100   0.246  -1.831  1.00  0.00           H  
HETATM   32  H8  UNL     1       6.452   1.226  -0.658  1.00  0.00           H  
HETATM   33  H9  UNL     1       4.996  -2.604   0.496  1.00  0.00           H  
HETATM   34  H10 UNL     1       1.229  -1.470   0.869  1.00  0.00           H  
HETATM   35  H11 UNL     1       2.830  -0.959   2.331  1.00  0.00           H  
HETATM   36  H12 UNL     1      -0.610  -0.266   1.977  1.00  0.00           H  
HETATM   37  H13 UNL     1      -0.382   2.205   1.747  1.00  0.00           H  
HETATM   38  H14 UNL     1      -2.835   1.910   0.428  1.00  0.00           H  
CONECT    1    2   25   26
CONECT    2    3    3   24
CONECT    3    4
CONECT    4    5    5    6
CONECT    6    7   23   23
CONECT    7    8    8
CONECT    8    9   27
CONECT    9   10   23
CONECT   10   11   21   28
CONECT   11   12
CONECT   12   13   19   29
CONECT   13   14   30   31
CONECT   14   15
CONECT   15   16   16   17   18
CONECT   17   32
CONECT   18   33
CONECT   19   20   21   34
CONECT   20   35
CONECT   21   22   36
CONECT   22   37
CONECT   23   24
CONECT   24   38
END

HMDB0060415
     RDKit          3D
6-Thioguanosine monophosphate
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.2270    1.9531   -1.9416 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0211    0.9503   -0.9127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0874    0.3375   -0.3046 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0155   -0.5530    0.6882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2770   -1.3625    1.3172 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7096   -0.8302    1.0933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2452   -1.6840    2.0348 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9042   -1.6410    2.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5546   -0.7417    1.0433 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1612   -0.5729    0.6687 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3652    0.5936    0.3210 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6150    0.1999   -0.0623 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7033    1.0703   -0.5044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0413    1.9330    0.5746 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7456    1.8204    0.7594 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.8964    1.5543    2.2721 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6511    3.0602    0.2346 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2617    0.3565   -0.0123 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4485   -1.0180   -0.9337 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2493   -2.0612   -0.4520 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0151   -1.3318   -0.6981 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3606   -2.6563   -0.5759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6265   -0.2557    0.5181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7808    0.6359   -0.4860 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1353    2.9461   -1.6582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4366    1.7326   -2.9388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3104   -2.2343    2.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5337   -1.1107    1.3431 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0130   -0.2572    0.9907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3137    1.7902   -1.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5709    0.5713   -0.8982 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5823    3.4076   -0.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7499   -0.3814    0.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6928   -0.7947   -1.9892 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7177   -2.7476   -0.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5926   -0.7708   -1.4667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7181   -3.0211   -1.3975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9724    1.1134   -0.9278 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
  4  6  1  0
  6  7  1  0
  7  8  2  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  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 12 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
  9 23  1  0
 23 24  1  0
 24  2  1  0
 23  6  2  0
 21 10  1  0
  1 25  1  0
  1 26  1  0
  8 27  1  0
 10 28  1  1
 12 29  1  1
 13 30  1  0
 13 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  6
 20 35  1  0
 21 36  1  6
 22 37  1  0
 24 38  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
6-Thioguanosine monophosphoric acid	Generator
6-TG Nucleotide	HMDB
6-Thioguanine nucleotide	HMDB
6-Thioguanosine-5'-phosphate	HMDB

Chemical Formula

C₁₀H₁₄N₅O₇PS

Average Molecular Weight

379.286

Monoisotopic Molecular Weight

379.035155029

IUPAC Name

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

Traditional Name

[(2R,3S,4R,5R)-5-(2-amino-6-sulfanylidene-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

NC1=NC(=S)C2=C(N1)N(C=N2)[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O

InChI Identifier

InChI=1S/C10H14N5O7PS/c11-10-13-7-4(8(24)14-10)12-2-15(7)9-6(17)5(16)3(22-9)1-21-23(18,19)20/h2-3,5-6,9,16-17H,1H2,(H2,18,19,20)(H3,11,13,14,24)/t3-,5-,6-,9-/m1/s1

InChI Key

BPZXYEUJBFHASJ-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
Monosaccharide phosphate
Pentose monosaccharide
Purinethione
Imidazopyrimidine
Purine
Aminopyrimidine
Monoalkyl phosphate
Pyrimidinethione
Alkyl phosphate
Pyrimidine
Phosphoric acid ester
Monosaccharide
N-substituted imidazole
Organic phosphoric acid derivative
Tetrahydrofuran
Azole
Imidazole
Heteroaromatic compound
Secondary alcohol
1,2-diol
Organoheterocyclic compound
Azacycle
Oxacycle
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Amine
Organic oxygen compound
Organic nitrogen compound
Primary amine
Alcohol
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

organic molecule (CHEBI:80613 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (HMDB: HMDB0060789)

Organ

Kidney (HMDB: HMDB0060789)
Liver (HMDB: HMDB0060789)

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0060789)

Cellular substructure

Cytoplasm (HMDB: HMDB0060789)

Source

Endogenous

Endogenous (HMDB: HMDB0060789)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.81 g/L	ALOGPS
logP	-1.4	ALOGPS
logP	-3.6	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	1.23	ChemAxon
pKa (Strongest Basic)	3.39	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	184.68 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	83.05 m³·mol⁻¹	ChemAxon
Polarizability	33.25 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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]+	182.768	31661259
DarkChem	[M-H]-	175.459	31661259
DeepCCS	[M+H]+	169.899	30932474
DeepCCS	[M-H]-	167.503	30932474
DeepCCS	[M-2H]-	201.225	30932474
DeepCCS	[M+Na]+	176.685	30932474
AllCCS	[M+H]+	180.3	32859911
AllCCS	[M+H-H2O]+	177.5	32859911
AllCCS	[M+NH4]+	182.8	32859911
AllCCS	[M+Na]+	183.5	32859911
AllCCS	[M-H]-	174.3	32859911
AllCCS	[M+Na-2H]-	174.1	32859911
AllCCS	[M+HCOO]-	174.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
6-Thioguanosine monophosphate	NC1=NC(=S)C2=C(N1)N(C=N2)[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O	4624.4	Standard polar	33892256
6-Thioguanosine monophosphate	NC1=NC(=S)C2=C(N1)N(C=N2)[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O	2407.1	Standard non polar	33892256
6-Thioguanosine monophosphate	NC1=NC(=S)C2=C(N1)N(C=N2)[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O	3826.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
6-Thioguanosine monophosphate,1TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@@H]1O	3367.9	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@@H]1O	3367.9	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3352.0	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3352.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TMS,isomer #3	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@H](O)[C@@H]1O	3459.6	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TMS,isomer #3	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@H](O)[C@@H]1O	3459.6	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TMS,isomer #4	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2	3399.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TMS,isomer #4	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2	3399.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TMS,isomer #5	C[Si](C)(C)N1C(N)=NC(=S)C2=C1N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2	3332.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TMS,isomer #5	C[Si](C)(C)N1C(N)=NC(=S)C2=C1N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2	3332.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3250.6	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3250.6	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #10	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O	3382.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #10	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O	3382.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #11	C[Si](C)(C)N(C1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2)[Si](C)(C)C	3293.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #11	C[Si](C)(C)N(C1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2)[Si](C)(C)C	3293.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #12	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C	3338.9	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #12	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C	3338.9	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3363.1	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3363.1	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #3	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N2	3257.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #3	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N2	3257.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O	3259.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O	3259.2	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3351.0	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3351.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #6	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N2	3236.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #6	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N2	3236.5	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC2=S	3237.3	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC2=S	3237.3	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #8	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3403.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #8	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3403.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #9	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N2	3374.3	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TMS,isomer #9	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N2	3374.3	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3285.5	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3351.0	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	5132.9	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #10	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N2	3283.3	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #10	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N2	3445.0	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #10	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N2	5021.1	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC2=S	3277.4	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC2=S	3406.5	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC2=S	5296.7	Standard polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3202.6	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3692.5	Standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	5309.8	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #13	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3201.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #13	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3614.3	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #13	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	5391.2	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #14	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N2	3339.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #14	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N2	3453.2	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #14	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N2	4817.3	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #15	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3340.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #15	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3416.6	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #15	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	5151.8	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	3294.3	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	3610.5	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	4998.5	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #17	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C	3363.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #17	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C	3549.9	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #17	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C	5087.7	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #18	C[Si](C)(C)N(C1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C)[Si](C)(C)C	3300.6	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #18	C[Si](C)(C)N(C1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C)[Si](C)(C)C	3780.9	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #18	C[Si](C)(C)N(C1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C)[Si](C)(C)C	5417.8	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #2	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N2	3162.9	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #2	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N2	3517.9	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #2	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N2	5350.2	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3143.6	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3464.5	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	5609.8	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3331.1	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3337.8	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	4917.6	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #5	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N2	3288.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #5	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N2	3430.7	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #5	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N2	4995.5	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O	3303.4	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O	3395.5	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O	5274.8	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3219.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3682.3	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	5289.0	Standard polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #8	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C	3225.7	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #8	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C	3603.8	Standard non polar	33892256
6-Thioguanosine monophosphate,3TMS,isomer #8	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C	5376.9	Standard polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3316.1	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3348.0	Standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	4950.6	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3265.2	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3228.1	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	4775.6	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3230.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3678.9	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	4967.5	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #11	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N2	3292.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #11	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N2	3336.4	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #11	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N2	4506.5	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC2=S	3263.2	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC2=S	3287.8	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC2=S	4902.1	Standard polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3256.5	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3516.6	Standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	4667.1	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #14	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3287.9	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #14	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3432.5	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #14	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	4756.8	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3215.3	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3685.7	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	4981.4	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #16	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3299.3	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #16	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3508.1	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #16	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	4470.5	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #17	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C	3357.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #17	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C	3423.6	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #17	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C	4564.3	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #18	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	3349.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #18	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	3612.3	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #18	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	4738.5	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #2	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N2	3249.7	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #2	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N2	3355.6	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #2	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N2	4726.6	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3226.7	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3308.4	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	5094.3	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3182.4	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3602.2	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	4926.4	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #5	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3174.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #5	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3506.9	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #5	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	5024.8	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #6	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N2	3294.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #6	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N2	3321.9	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #6	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N2	4468.0	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O	3281.7	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O	3279.0	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O	4873.8	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3262.2	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3506.3	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	4643.1	Standard polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #9	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C	3300.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #9	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C	3421.0	Standard non polar	33892256
6-Thioguanosine monophosphate,4TMS,isomer #9	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C	4737.8	Standard polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #1	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N2	3287.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #1	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N2	3245.0	Standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #1	C[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N2	4251.8	Standard polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #10	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3337.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #10	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3314.9	Standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #10	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	4277.5	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3323.8	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3515.5	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	4392.5	Standard polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3377.1	Semi standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3484.3	Standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C	4249.8	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3256.2	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	3196.2	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C	4750.3	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3263.4	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3435.4	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	4353.7	Standard polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #4	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3288.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #4	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3337.3	Standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #4	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	4457.1	Standard polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3226.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3585.1	Standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	4592.0	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3300.9	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3393.2	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	4142.3	Standard polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #7	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C	3344.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #7	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C	3302.8	Standard non polar	33892256
6-Thioguanosine monophosphate,5TMS,isomer #7	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C	4243.0	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3334.3	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3506.1	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	4373.3	Standard polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3299.7	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3409.4	Standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	4181.8	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3328.5	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3331.2	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3968.4	Standard polar	33892256
6-Thioguanosine monophosphate,6TMS,isomer #2	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3365.1	Semi standard non polar	33892256
6-Thioguanosine monophosphate,6TMS,isomer #2	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	3234.3	Standard non polar	33892256
6-Thioguanosine monophosphate,6TMS,isomer #2	C[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=N2)N1[Si](C)(C)C	4043.1	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3344.6	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3436.2	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	4114.7	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3396.6	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3399.0	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O	3949.1	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3384.2	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3409.3	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=S	3982.1	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3424.2	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3325.8	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C	3811.0	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3613.7	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3613.7	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3596.2	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3596.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@H](O)[C@@H]1O	3673.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@H](O)[C@@H]1O	3673.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2	3588.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2	3588.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N1C(N)=NC(=S)C2=C1N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2	3600.9	Semi standard non polar	33892256
6-Thioguanosine monophosphate,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N1C(N)=NC(=S)C2=C1N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2	3600.9	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3733.1	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3733.1	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O	3785.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O	3785.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2)[Si](C)(C)C(C)(C)C	3704.1	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N2)[Si](C)(C)C(C)(C)C	3704.1	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C	3739.6	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C	3739.6	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3791.7	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3791.7	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C=N2	3659.3	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C=N2	3659.3	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O	3729.1	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O	3729.1	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3777.6	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3777.6	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C=N2	3646.7	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C=N2	3646.7	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC2=S	3707.4	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC2=S	3707.4	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3802.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3802.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)C=N2	3748.1	Semi standard non polar	33892256
6-Thioguanosine monophosphate,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)C=N2	3748.1	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3870.7	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3832.4	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	5169.8	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C=N2	3848.4	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C=N2	4025.2	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C=N2	5048.8	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC2=S	3883.4	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC2=S	3930.4	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC2=S	5288.4	Standard polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=S	3785.7	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=S	4201.1	Standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=S	5203.1	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C=N2)N1[Si](C)(C)C(C)(C)C	3818.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C=N2)N1[Si](C)(C)C(C)(C)C	4169.3	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C=N2)N1[Si](C)(C)C(C)(C)C	5259.2	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O)C=N2	3894.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O)C=N2	3960.2	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O)C=N2	4906.8	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3923.5	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3878.7	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	5161.6	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	3856.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	4123.6	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	5001.6	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C	3921.7	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C	4103.0	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C	5055.7	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3895.3	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4262.5	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5242.9	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)C=N2	3747.9	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)C=N2	4087.6	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)C=N2	5275.2	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3820.5	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3983.5	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	5543.9	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3892.5	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	3777.3	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O	4985.9	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O)C=N2	3851.1	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O)C=N2	4008.0	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O)C=N2	5026.5	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O	3901.1	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O	3923.2	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O	5263.7	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O	3793.4	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O	4188.2	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O	5185.8	Standard polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C	3831.3	Semi standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C	4164.9	Standard non polar	33892256
6-Thioguanosine monophosphate,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C=N2)N1[Si](C)(C)C(C)(C)C	5245.3	Standard polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3881.2	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	3787.4	Standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N)=NC2=S	5021.1	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3992.7	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3765.2	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	4861.2	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O	4024.1	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O	4294.0	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O	4878.4	Standard polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O[Si](C)(C)C(C)(C)C)C=N2	4027.2	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O[Si](C)(C)C(C)(C)C)C=N2	3972.9	Standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O[Si](C)(C)C(C)(C)C)C=N2	4669.8	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC2=S	4032.9	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC2=S	3879.3	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC2=S	4959.2	Standard polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=S	3985.4	Semi standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=S	4160.1	Standard non polar	33892256
6-Thioguanosine 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=C1[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=S	4696.4	Standard polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C=N2)N1[Si](C)(C)C(C)(C)C	4040.7	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C=N2)N1[Si](C)(C)C(C)(C)C	4113.5	Standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C=N2)N1[Si](C)(C)C(C)(C)C	4771.7	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=S	4017.9	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=S	4297.9	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=S	4890.7	Standard polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	4006.4	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	4081.2	Standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	4596.2	Standard polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[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]3O)C=N2)N1[Si](C)(C)C(C)(C)C	4071.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[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]3O)C=N2)N1[Si](C)(C)C(C)(C)C	4043.7	Standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[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]3O)C=N2)N1[Si](C)(C)C(C)(C)C	4666.0	Standard polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	4060.1	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	4230.9	Standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@H](O)[C@@H]1O	4746.7	Standard polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O[Si](C)(C)C(C)(C)C)C=N2	3986.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O[Si](C)(C)C(C)(C)C)C=N2	4039.5	Standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O[Si](C)(C)C(C)(C)C)C=N2	4802.0	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	4020.7	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3937.8	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	5094.7	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	3927.5	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	4222.3	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O[Si](C)(C)C(C)(C)C	4867.7	Standard polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C=N2)N1[Si](C)(C)C(C)(C)C	3946.8	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C=N2)N1[Si](C)(C)C(C)(C)C	4183.6	Standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C=N2)N1[Si](C)(C)C(C)(C)C	4948.1	Standard polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O)C=N2	4034.0	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O)C=N2	3954.0	Standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C([NH]1)N([C@@H]1O[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]1O)C=N2	4634.7	Standard polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O	4049.6	Semi standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O	3872.6	Standard non polar	33892256
6-Thioguanosine 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([Si](C)(C)C(C)(C)C)C(N)=NC3=S)[C@@H]1O	4930.7	Standard polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O	3989.1	Semi standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O	4145.8	Standard non polar	33892256
6-Thioguanosine 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=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=S)[C@@H]1O	4674.9	Standard polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[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]3O)C=N2)N1[Si](C)(C)C(C)(C)C	4048.4	Semi standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[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]3O)C=N2)N1[Si](C)(C)C(C)(C)C	4106.9	Standard non polar	33892256
6-Thioguanosine monophosphate,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC(=S)C2=C(N([C@@H]3O[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]3O)C=N2)N1[Si](C)(C)C(C)(C)C	4754.3	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Thioguanosine monophosphate GC-MS (Non-derivatized) - 70eV, Positive	splash10-01ot-9532000000-554f8c59640cc644586e	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Thioguanosine monophosphate GC-MS (2 TMS) - 70eV, Positive	splash10-01ot-9311200000-aa4075f5626be7ed4fbe	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Thioguanosine monophosphate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Thioguanosine monophosphate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Thioguanosine 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
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 10V, Positive-QTOF	splash10-014i-0913000000-96a4f72bf492be7f7409	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 20V, Positive-QTOF	splash10-014i-0900000000-dfebaa4c8fd99d57db92	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 40V, Positive-QTOF	splash10-014i-1900000000-f58433842072d381834e	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 10V, Negative-QTOF	splash10-004i-6519000000-238224e8d8f10e7d2ce2	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 20V, Negative-QTOF	splash10-00or-9700000000-001e7924823178c2fa60	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 40V, Negative-QTOF	splash10-004i-9100000000-37c3f1a5f378f4931d75	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 10V, Positive-QTOF	splash10-014i-0902000000-30c23e5a6559ccfe66be	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 20V, Positive-QTOF	splash10-014i-0900000000-1be32560b8ce9213242d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 40V, Positive-QTOF	splash10-014i-2900000000-5d61f3ef8b8db880c9cf	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 10V, Negative-QTOF	splash10-004i-8009000000-e5d582d7d7e58132d773	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 20V, Negative-QTOF	splash10-004i-9011000000-3b33f78bf4d38dada3c3	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Thioguanosine monophosphate 40V, Negative-QTOF	splash10-004i-9100000000-261c2e81600445e5233e	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Urine

Tissue Locations

Kidney
Liver

Pathways

Name	SMPDB/PathBank	KEGG
Mercaptopurine Action Pathway		Not Available
Mercaptopurine Metabolism Pathway		Not Available
Thioguanine Action Pathway		Not Available
Azathioprine Action Pathway		Not Available
Thioguanine Metabolism Pathway		Not Available

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Available	Not Available	Normal	Not Available	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Normal	Not Available	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C16619

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3034646

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Magrane M: UniProt Knowledgebase: a hub of integrated protein data. Database (Oxford). 2011 Mar 29;2011:bar009. doi: 10.1093/database/bar009. Print 2011. [PubMed:21447597 ]

Enzymes

Enzyme Details

1. Thiopurine S-methyltransferase

General function:: Involved in thiopurine S-methyltransferase activity
Specific function:: Catalyzes the S-methylation of thiopurine drugs such as 6-mercaptopurine.
Gene Name:: TPMT
Uniprot ID:: P51580
Molecular weight:: 28180.09

Reactions

6-Thioguanosine monophosphate + S-Adenosylmethionine → 6-Methylthioguanosine monophosphate + S-Adenosylhomocysteine	details

Enzyme Details

2. Hypoxanthine-guanine phosphoribosyltransferase

General function:: Involved in hypoxanthine phosphoribosyltransferase activity
Specific function:: Converts guanine to guanosine monophosphate, and hypoxanthine to inosine monophosphate. Transfers the 5-phosphoribosyl group from 5-phosphoribosylpyrophosphate onto the purine. Plays a central role in the generation of purine nucleotides through the purine salvage pathway.
Gene Name:: HPRT1
Uniprot ID:: P00492
Molecular weight:: 24579.155

Reactions

Thioguanine + Phosphoribosyl pyrophosphate → 6-Thioguanosine monophosphate + Pyrophosphate	details

Enzyme Details

3. GMP synthase [glutamine-hydrolyzing]

General function:: Involved in catalytic activity
Specific function:: Involved in the de novo synthesis of guanine nucleotides which are not only essential for DNA and RNA synthesis, but also provide GTP, which is involved in a number of cellular processes important for cell division.
Gene Name:: GMPS
Uniprot ID:: P49915
Molecular weight:: 76714.79

Reactions

6-Thioxanthine 5'-monophosphate + Adenosine triphosphate + Glutamine + Water → 6-Thioguanosine monophosphate + Adenosine monophosphate + Pyrophosphate + Glutamic acid	details

Showing metabocard for 6-Thioguanosine monophosphate (HMDB0060415)

MOL for HMDB0060415 (6-Thioguanosine monophosphate)

3D MOL for HMDB0060415 (6-Thioguanosine monophosphate)

3D SDF for HMDB0060415 (6-Thioguanosine monophosphate)

3D-SDF for HMDB0060415 (6-Thioguanosine monophosphate)

PDB for HMDB0060415 (6-Thioguanosine monophosphate)

3D PDB for HMDB0060415 (6-Thioguanosine monophosphate)

SMILES for HMDB0060415 (6-Thioguanosine monophosphate)

INCHI for HMDB0060415 (6-Thioguanosine monophosphate)

Structure for HMDB0060415 (6-Thioguanosine monophosphate)

3D Structure for HMDB0060415 (6-Thioguanosine monophosphate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions

Reactions

Reactions