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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (4) Show 4 proteins XML

enzymes (4) Show 4 proteins

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2009-02-04 09:30:46 UTC

Update Date

2021-09-14 14:57:17 UTC

HMDB ID

HMDB0011670

Secondary Accession Numbers

HMDB11670

Metabolite Identification

Common Name

8-Oxo-dGMP

Description

8-Oxo-dGMP is a metabolite of 8-oxo-dGTP. 8-Oxo-7,8-dihydro-2'-deoxyguanosine 5'-triphosphate (8-oxo-dGTP) is a potent mutagenic substrate for DNA synthesis. 8-Oxo-dGTP is rapidly degraded to 8-oxo-dGMP by cellular 8-oxo-dGTPase activity. 8-Oxo-dGMP is further degraded to 8-oxo-deoxyguanosine by a nucleotidase. 8-Oxo-dGMP is the most preferred substrate of this nucleotidase enzyme (PMID: 7819228 ). The human MutT homologue (hMTH1), an 8-oxo-dGTPase, prevents misincorporation of 8-oxo-dGTP into DNA by hydrolyzing it to 8-oxo-dGMP. hMTH1 mRNA is overexpressed in human renal cell carcinomas and breast tumors. Likewise, elevated levels of hMTH1 protein have also been detected in brain tumors. (PMID: 12757855 ).

Structure

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

HMDB0011670
     RDKit          3D
8-Oxo-dGMP
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.3382    2.4822   -0.4116 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1703    1.0834   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1883    0.2060   -0.5528 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9917   -1.1214   -0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9206   -1.9450   -0.6903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6737   -1.6236   -0.5060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1404   -2.8246   -0.5076 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8119   -2.7083   -0.3767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0322   -3.6926   -0.3325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4980   -1.3747   -0.2977 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2619   -0.8969    0.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1522    0.5114    0.5298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2265    0.2790    1.2189 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7915    1.5340    1.4280 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8409   -0.4166    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6617    0.6150   -0.6682 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7667   -0.0300   -1.2752 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1131    0.6747   -0.4077 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.7926    0.3013    1.1000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2189    2.2909   -0.5091 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4496   -0.2444   -0.7728 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8949   -0.9883   -0.7760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493   -0.7242   -0.3924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9536    0.5854   -0.3757 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5369    3.1310   -0.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2864    2.8777   -0.2854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6966   -3.7043   -0.5804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1044   -1.5162    0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1535    1.2656   -0.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8729    0.7767    1.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1302   -0.3394    2.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3042    1.5145    2.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5604   -1.2259    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095    0.9611   -1.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230    1.5345   -0.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1549    2.6575   -0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2342   -1.1807   -0.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1556    1.2752   -0.3571 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  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 18 21  1  0
 15 22  1  0
 10 23  1  0
 23 24  1  0
 24  2  1  0
 23  6  2  0
 22 11  1  0
  1 25  1  0
  1 26  1  0
  7 27  1  0
 11 28  1  0
 12 29  1  0
 12 30  1  0
 13 31  1  1
 14 32  1  0
 15 33  1  0
 16 34  1  0
 16 35  1  0
 20 36  1  0
 21 37  1  0
 24 38  1  0
M  END


  Mrv0541 02241201492D          

 24 26  0  0  1  0            999 V2000
   13.4695   -4.2214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8821   -4.9358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6445   -4.2214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4695   -5.6504    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.2320   -4.9358    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.6445   -5.6504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0216   -3.6083    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.7753   -3.9438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6891   -4.7643    0.0000 N   0  0  2  0  0  0  0  0  0  0  0  0
   12.2320   -3.5069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4898   -3.5313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2320   -6.3648    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.3022   -5.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1091   -5.1448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2159   -6.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9696   -6.4724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.5216   -5.8593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1411   -7.2794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.3421   -5.9456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6777   -6.6992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4982   -6.7855    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   18.4120   -7.6059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.5844   -5.9650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.3187   -6.8717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  6  5  2  0  0  0  0
  7  1  1  0  0  0  0
  2  1  2  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
  9  2  1  0  0  0  0
 10  3  2  0  0  0  0
 11  8  2  0  0  0  0
 12  6  1  0  0  0  0
  9 13  1  6  0  0  0
 15 13  1  0  0  0  0
 14 13  1  0  0  0  0
 16 15  1  0  0  0  0
 17 14  1  0  0  0  0
 17 16  1  0  0  0  0
 16 18  1  1  0  0  0
 19 17  1  0  0  0  0
 22 21  2  0  0  0  0
 23 21  1  0  0  0  0
 24 21  1  0  0  0  0
 20 21  1  0  0  0  0
 19 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0011670

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=NC(=O)C2=C(N1)N(C1C[C@H](O)C(COP(O)(O)=O)O1)C(=O)N2

> <INCHI_IDENTIFIER>
InChI=1S/C10H14N5O8P/c11-9-13-7-6(8(17)14-9)12-10(18)15(7)5-1-3(16)4(23-5)2-22-24(19,20)21/h3-5,16H,1-2H2,(H,12,18)(H2,19,20,21)(H3,11,13,14,17)/t3-,4?,5?/m0/s1

> <INCHI_KEY>
AQIVLFLYHYFRKU-KLFYCJEISA-N

> <FORMULA>
C10H14N5O8P

> <MOLECULAR_WEIGHT>
363.2206

> <EXACT_MASS>
363.057998961

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
30.657131487553443

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(3S)-5-(2-amino-6,8-dioxo-6,7,8,9-tetrahydro-3H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}phosphonic acid

> <ALOGPS_LOGP>
-1.42

> <JCHEM_LOGP>
-3.5766463929517296

> <ALOGPS_LOGS>
-1.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.235017332411092

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.284118870061798

> <JCHEM_PKA_STRONGEST_BASIC>
2.5860690099456285

> <JCHEM_POLAR_SURFACE_AREA>
196.03999999999996

> <JCHEM_REFRACTIVITY>
83.5663

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.97e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(3S)-5-(2-amino-6,8-dioxo-3,7-dihydropurin-9-yl)-3-hydroxyoxolan-2-yl]methoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0011670
     RDKit          3D
8-Oxo-dGMP
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.3382    2.4822   -0.4116 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1703    1.0834   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1883    0.2060   -0.5528 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9917   -1.1214   -0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9206   -1.9450   -0.6903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6737   -1.6236   -0.5060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1404   -2.8246   -0.5076 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8119   -2.7083   -0.3767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0322   -3.6926   -0.3325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4980   -1.3747   -0.2977 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2619   -0.8969    0.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1522    0.5114    0.5298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2265    0.2790    1.2189 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7915    1.5340    1.4280 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8409   -0.4166    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6617    0.6150   -0.6682 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7667   -0.0300   -1.2752 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1131    0.6747   -0.4077 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.7926    0.3013    1.1000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2189    2.2909   -0.5091 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4496   -0.2444   -0.7728 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8949   -0.9883   -0.7760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493   -0.7242   -0.3924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9536    0.5854   -0.3757 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5369    3.1310   -0.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2864    2.8777   -0.2854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6966   -3.7043   -0.5804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1044   -1.5162    0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1535    1.2656   -0.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8729    0.7767    1.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1302   -0.3394    2.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3042    1.5145    2.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5604   -1.2259    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095    0.9611   -1.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230    1.5345   -0.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1549    2.6575   -0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2342   -1.1807   -0.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1556    1.2752   -0.3571 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  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 18 21  1  0
 15 22  1  0
 10 23  1  0
 23 24  1  0
 24  2  1  0
 23  6  2  0
 22 11  1  0
  1 25  1  0
  1 26  1  0
  7 27  1  0
 11 28  1  0
 12 29  1  0
 12 30  1  0
 13 31  1  1
 14 32  1  0
 15 33  1  0
 16 34  1  0
 16 35  1  0
 20 36  1  0
 21 37  1  0
 24 38  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      25.143  -7.880   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      25.913  -9.213   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      23.603  -7.880   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      25.143 -10.547   0.000  0.00  0.00           N+0
HETATM    5  N   UNK     0      22.833  -9.213   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      23.603 -10.547   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      26.174  -6.735   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      27.581  -7.362   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      27.420  -8.893   0.000  0.00  0.00           N+0
HETATM   10  O   UNK     0      22.833  -6.546   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      28.914  -6.592   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0      22.833 -11.881   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      28.564  -9.924   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      30.070  -9.604   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      28.403 -11.456   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      29.810 -12.082   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      30.840 -10.937   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      30.130 -13.588   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      32.372 -11.098   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      32.998 -12.505   0.000  0.00  0.00           O+0
HETATM   21  P   UNK     0      34.530 -12.666   0.000  0.00  0.00           P+0
HETATM   22  O   UNK     0      34.369 -14.198   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      34.691 -11.135   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      36.062 -12.827   0.000  0.00  0.00           O+0
CONECT    1    3    7    2                                                  
CONECT    2    4    1    9                                                  
CONECT    3    1    5   10                                                  
CONECT    4    2    6                                                       
CONECT    5    3    6                                                       
CONECT    6    4    5   12                                                  
CONECT    7    1    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8    2   13                                                  
CONECT   10    3                                                            
CONECT   11    8                                                            
CONECT   12    6                                                            
CONECT   13    9   15   14                                                  
CONECT   14   13   17                                                       
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   14   16   19                                                  
CONECT   18   16                                                            
CONECT   19   17   20                                                       
CONECT   20   21   19                                                       
CONECT   21   22   23   24   20                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

COMPND    HMDB0011670
HETATM    1  N1  UNL     1      -4.338   2.482  -0.412  1.00  0.00           N  
HETATM    2  C1  UNL     1      -4.170   1.083  -0.444  1.00  0.00           C  
HETATM    3  N2  UNL     1      -5.188   0.206  -0.553  1.00  0.00           N  
HETATM    4  C2  UNL     1      -4.992  -1.121  -0.589  1.00  0.00           C  
HETATM    5  O1  UNL     1      -5.921  -1.945  -0.690  1.00  0.00           O  
HETATM    6  C3  UNL     1      -3.674  -1.624  -0.506  1.00  0.00           C  
HETATM    7  N3  UNL     1      -3.140  -2.825  -0.508  1.00  0.00           N  
HETATM    8  C4  UNL     1      -1.812  -2.708  -0.377  1.00  0.00           C  
HETATM    9  O2  UNL     1      -1.032  -3.693  -0.333  1.00  0.00           O  
HETATM   10  N4  UNL     1      -1.498  -1.375  -0.298  1.00  0.00           N  
HETATM   11  C5  UNL     1      -0.262  -0.897   0.000  1.00  0.00           C  
HETATM   12  C6  UNL     1      -0.152   0.511   0.530  1.00  0.00           C  
HETATM   13  C7  UNL     1       1.227   0.279   1.219  1.00  0.00           C  
HETATM   14  O3  UNL     1       1.791   1.534   1.428  1.00  0.00           O  
HETATM   15  C8  UNL     1       1.841  -0.417   0.022  1.00  0.00           C  
HETATM   16  C9  UNL     1       2.662   0.615  -0.668  1.00  0.00           C  
HETATM   17  O4  UNL     1       3.767  -0.030  -1.275  1.00  0.00           O  
HETATM   18  P1  UNL     1       5.113   0.675  -0.408  1.00  0.00           P  
HETATM   19  O5  UNL     1       4.793   0.301   1.100  1.00  0.00           O  
HETATM   20  O6  UNL     1       5.219   2.291  -0.509  1.00  0.00           O  
HETATM   21  O7  UNL     1       6.450  -0.244  -0.773  1.00  0.00           O  
HETATM   22  O8  UNL     1       0.895  -0.988  -0.776  1.00  0.00           O  
HETATM   23  C10 UNL     1      -2.649  -0.724  -0.392  1.00  0.00           C  
HETATM   24  N5  UNL     1      -2.954   0.585  -0.376  1.00  0.00           N  
HETATM   25  H1  UNL     1      -3.537   3.131  -0.519  1.00  0.00           H  
HETATM   26  H2  UNL     1      -5.286   2.878  -0.285  1.00  0.00           H  
HETATM   27  H3  UNL     1      -3.697  -3.704  -0.580  1.00  0.00           H  
HETATM   28  H4  UNL     1       0.104  -1.516   0.941  1.00  0.00           H  
HETATM   29  H5  UNL     1       0.154   1.266  -0.216  1.00  0.00           H  
HETATM   30  H6  UNL     1      -0.873   0.777   1.281  1.00  0.00           H  
HETATM   31  H7  UNL     1       1.130  -0.339   2.103  1.00  0.00           H  
HETATM   32  H8  UNL     1       2.304   1.514   2.267  1.00  0.00           H  
HETATM   33  H9  UNL     1       2.560  -1.226   0.420  1.00  0.00           H  
HETATM   34  H10 UNL     1       2.010   0.961  -1.614  1.00  0.00           H  
HETATM   35  H11 UNL     1       2.923   1.534  -0.233  1.00  0.00           H  
HETATM   36  H12 UNL     1       6.155   2.657  -0.556  1.00  0.00           H  
HETATM   37  H13 UNL     1       6.234  -1.181  -0.422  1.00  0.00           H  
HETATM   38  H14 UNL     1      -2.156   1.275  -0.357  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   27
CONECT    8    9    9   10
CONECT   10   11   23
CONECT   11   12   22   28
CONECT   12   13   29   30
CONECT   13   14   15   31
CONECT   14   32
CONECT   15   16   22   33
CONECT   16   17   34   35
CONECT   17   18
CONECT   18   19   19   20   21
CONECT   20   36
CONECT   21   37
CONECT   23   24
CONECT   24   38
END

HMDB0011670
     RDKit          3D
8-Oxo-dGMP
 38 40  0  0  0  0  0  0  0  0999 V2000
   -4.3382    2.4822   -0.4116 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1703    1.0834   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1883    0.2060   -0.5528 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9917   -1.1214   -0.5891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9206   -1.9450   -0.6903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6737   -1.6236   -0.5060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1404   -2.8246   -0.5076 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8119   -2.7083   -0.3767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0322   -3.6926   -0.3325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4980   -1.3747   -0.2977 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2619   -0.8969    0.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1522    0.5114    0.5298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2265    0.2790    1.2189 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7915    1.5340    1.4280 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8409   -0.4166    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6617    0.6150   -0.6682 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7667   -0.0300   -1.2752 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1131    0.6747   -0.4077 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.7926    0.3013    1.1000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2189    2.2909   -0.5091 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4496   -0.2444   -0.7728 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8949   -0.9883   -0.7760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6493   -0.7242   -0.3924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9536    0.5854   -0.3757 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5369    3.1310   -0.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2864    2.8777   -0.2854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6966   -3.7043   -0.5804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1044   -1.5162    0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1535    1.2656   -0.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8729    0.7767    1.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1302   -0.3394    2.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3042    1.5145    2.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5604   -1.2259    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095    0.9611   -1.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230    1.5345   -0.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1549    2.6575   -0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2342   -1.1807   -0.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1556    1.2752   -0.3571 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  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 18 21  1  0
 15 22  1  0
 10 23  1  0
 23 24  1  0
 24  2  1  0
 23  6  2  0
 22 11  1  0
  1 25  1  0
  1 26  1  0
  7 27  1  0
 11 28  1  0
 12 29  1  0
 12 30  1  0
 13 31  1  1
 14 32  1  0
 15 33  1  0
 16 34  1  0
 16 35  1  0
 20 36  1  0
 21 37  1  0
 24 38  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
8-oxo-7,8-Dihydro-2'-deoxyguanosine 5'-triphosphate	HMDB
8OG	HMDB
{[(3S)-5-(6,8-dihydroxy-2-imino-3,9-dihydro-2H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}phosphonate	HMDB

Chemical Formula

C₁₀H₁₄N₅O₈P

Average Molecular Weight

363.2206

Monoisotopic Molecular Weight

363.057998961

IUPAC Name

{[(3S)-5-(2-amino-6,8-dioxo-6,7,8,9-tetrahydro-3H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}phosphonic acid

Traditional Name

[(3S)-5-(2-amino-6,8-dioxo-3,7-dihydropurin-9-yl)-3-hydroxyoxolan-2-yl]methoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

NC1=NC(=O)C2=C(N1)N(C1C[C@H](O)C(COP(O)(O)=O)O1)C(=O)N2

InChI Identifier

InChI=1S/C10H14N5O8P/c11-9-13-7-6(8(17)14-9)12-10(18)15(7)5-1-3(16)4(23-5)2-22-24(19,20)21/h3-5,16H,1-2H2,(H,12,18)(H2,19,20,21)(H3,11,13,14,17)/t3-,4?,5?/m0/s1

InChI Key

AQIVLFLYHYFRKU-KLFYCJEISA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Sub Class

Purine deoxyribonucleotides

Direct Parent

Purine 2'-deoxyribonucleoside monophosphates

Alternative Parents

Substituents

Purine 2'-deoxyribonucleoside monophosphate
6-oxopurine
Hypoxanthine
Purinone
Imidazopyrimidine
Purine
Aminopyrimidine
Monoalkyl phosphate
Pyrimidone
N-substituted imidazole
Organic phosphoric acid derivative
Phosphoric acid ester
Alkyl phosphate
Pyrimidine
Heteroaromatic compound
Azole
Imidazole
Vinylogous amide
Tetrahydrofuran
Urea
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Azacycle
Organopnictogen compound
Primary amine
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Amine
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Endogenous (HMDB: HMDB0011670)

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

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

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

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

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

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	5.97 g/L	ALOGPS
logP	-1.4	ALOGPS
logP	-3.6	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	1.28	ChemAxon
pKa (Strongest Basic)	2.59	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	196.04 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	83.57 m³·mol⁻¹	ChemAxon
Polarizability	30.66 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]+	179.092	31661259
DarkChem	[M-H]-	176.348	31661259
DeepCCS	[M+H]+	169.852	30932474
DeepCCS	[M-H]-	167.455	30932474
DeepCCS	[M-2H]-	202.028	30932474
DeepCCS	[M+Na]+	178.194	30932474
AllCCS	[M+H]+	176.8	32859911
AllCCS	[M+H-H2O]+	173.9	32859911
AllCCS	[M+NH4]+	179.4	32859911
AllCCS	[M+Na]+	180.2	32859911
AllCCS	[M-H]-	172.3	32859911
AllCCS	[M+Na-2H]-	171.9	32859911
AllCCS	[M+HCOO]-	171.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
8-Oxo-dGMP	NC1=NC(=O)C2=C(N1)N(C1C[C@H](O)C(COP(O)(O)=O)O1)C(=O)N2	4085.0	Standard polar	33892256
8-Oxo-dGMP	NC1=NC(=O)C2=C(N1)N(C1C[C@H](O)C(COP(O)(O)=O)O1)C(=O)N2	2164.9	Standard non polar	33892256
8-Oxo-dGMP	NC1=NC(=O)C2=C(N1)N(C1C[C@H](O)C(COP(O)(O)=O)O1)C(=O)N2	3812.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
8-Oxo-dGMP,1TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O	3187.6	Semi standard non polar	33892256
8-Oxo-dGMP,1TMS,isomer #2	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)C[C@@H]1O	3195.0	Semi standard non polar	33892256
8-Oxo-dGMP,1TMS,isomer #3	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	3153.2	Semi standard non polar	33892256
8-Oxo-dGMP,1TMS,isomer #4	C[Si](C)(C)N1C(N)=NC(=O)C2=C1N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	3147.2	Semi standard non polar	33892256
8-Oxo-dGMP,1TMS,isomer #5	C[Si](C)(C)N1C(=O)N(C2C[C@H](O)C(COP(=O)(O)O)O2)C2=C1C(=O)N=C(N)[NH]2	3214.1	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3173.3	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3276.1	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	5268.8	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #10	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3176.1	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #10	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3360.9	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #10	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	5774.5	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #11	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	3140.4	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #11	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	3482.2	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #11	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	5755.5	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #12	C[Si](C)(C)N1C(N)=NC(=O)C2=C1N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3203.1	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #12	C[Si](C)(C)N1C(N)=NC(=O)C2=C1N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3354.9	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #12	C[Si](C)(C)N1C(N)=NC(=O)C2=C1N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	5909.3	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #2	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	3114.1	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #2	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	3354.0	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #2	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	5675.8	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #3	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O	3182.4	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #3	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O	3213.7	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #3	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O	5671.4	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	3119.1	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	3333.4	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	5820.4	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #5	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3155.6	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #5	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3351.7	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #5	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	5115.0	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #6	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	3148.7	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #6	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	3386.7	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #6	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	5296.2	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #7	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O	3174.6	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #7	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O	3287.9	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #7	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O	5310.0	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #8	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O	3139.9	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #8	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O	3388.5	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #8	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O	5460.5	Standard polar	33892256
8-Oxo-dGMP,2TMS,isomer #9	C[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C	3098.9	Semi standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #9	C[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C	3506.3	Standard non polar	33892256
8-Oxo-dGMP,2TMS,isomer #9	C[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C	5683.5	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3134.6	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3255.6	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	4821.9	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #10	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3132.5	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #10	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3267.0	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #10	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	4829.3	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #11	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3111.7	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #11	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3389.8	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #11	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	4986.6	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #12	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	3110.2	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #12	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	3479.1	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #12	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	4848.2	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #13	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3132.4	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #13	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3316.8	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #13	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	4964.5	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #14	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	3116.0	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #14	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	3457.9	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #14	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	4945.7	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #15	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O	3171.7	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #15	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O	3324.1	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #15	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O	5197.6	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #16	C[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C)[Si](C)(C)C	3143.6	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #16	C[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C)[Si](C)(C)C	3483.8	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #16	C[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C)[Si](C)(C)C	5208.2	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #17	C[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C	3127.3	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #17	C[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C	3603.1	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #17	C[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C	5229.1	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #18	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3193.7	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #18	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3427.5	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #18	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	5352.6	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #2	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	3128.8	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #2	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	3299.8	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #2	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	4886.4	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #3	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3146.8	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #3	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3160.3	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #3	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	4987.0	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3113.4	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3287.7	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	5150.4	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #5	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	3064.7	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #5	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	3471.5	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #5	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	5140.4	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #6	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3123.6	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #6	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3263.7	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #6	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	5260.6	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #7	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	3092.6	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #7	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	3405.9	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #7	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	5242.4	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #8	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	3162.4	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #8	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	3248.7	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #8	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	5513.0	Standard polar	33892256
8-Oxo-dGMP,3TMS,isomer #9	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	3145.4	Semi standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #9	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	3387.7	Standard non polar	33892256
8-Oxo-dGMP,3TMS,isomer #9	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	4700.8	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #1	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	3141.2	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #1	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	3263.8	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #1	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	4344.2	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #10	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3172.0	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #10	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	3289.7	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #10	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C	4905.6	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #11	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3139.7	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #11	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3471.6	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #11	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	4303.9	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #12	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3165.7	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #12	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3286.1	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #12	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	4437.2	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #13	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	3151.4	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #13	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	3411.0	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #13	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	4407.3	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #14	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3178.3	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #14	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3274.3	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #14	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	4780.8	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #15	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	3166.4	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #15	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	3426.1	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #15	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	4522.3	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	3146.2	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	3553.4	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	4540.4	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #17	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3192.4	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #17	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3344.4	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #17	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	4686.4	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #18	C[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C)[Si](C)(C)C	3183.8	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #18	C[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C)[Si](C)(C)C	3533.1	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #18	C[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C)[Si](C)(C)C	4871.0	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #2	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3127.1	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #2	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3112.6	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #2	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	4589.3	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #3	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3116.3	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #3	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3232.7	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #3	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	4751.2	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3113.7	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3397.5	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	4454.1	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #5	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3149.6	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #5	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3182.6	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #5	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	4593.7	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #6	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	3129.5	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #6	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	3305.1	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #6	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)[NH]2	4566.9	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #7	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3179.2	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #7	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3188.2	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #7	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	4940.2	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #8	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	3109.7	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #8	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	3381.7	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #8	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	4718.2	Standard polar	33892256
8-Oxo-dGMP,4TMS,isomer #9	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	3098.9	Semi standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #9	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	3509.4	Standard non polar	33892256
8-Oxo-dGMP,4TMS,isomer #9	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	4739.9	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3173.7	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3357.4	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3979.9	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #10	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3204.4	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #10	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3511.7	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #10	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	4043.8	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #11	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3249.7	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #11	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3294.2	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #11	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	4195.1	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #12	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	3251.0	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #12	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	3454.4	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #12	C[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O	4260.9	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #2	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3203.8	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #2	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3151.7	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #2	C[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	4099.2	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #3	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	3186.9	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #3	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	3262.9	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #3	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)[NH]2	4072.2	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3213.8	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3138.7	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	4563.3	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #5	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3195.8	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #5	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3296.0	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #5	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	4121.9	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #6	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3186.3	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #6	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3428.9	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #6	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	4137.9	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #7	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3239.6	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #7	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3208.1	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #7	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	4298.6	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #8	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	3198.0	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #8	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	3410.8	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #8	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O	4386.7	Standard polar	33892256
8-Oxo-dGMP,5TMS,isomer #9	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3214.2	Semi standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #9	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3375.9	Standard non polar	33892256
8-Oxo-dGMP,5TMS,isomer #9	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	4029.1	Standard polar	33892256
8-Oxo-dGMP,6TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3264.4	Semi standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3250.3	Standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3751.4	Standard polar	33892256
8-Oxo-dGMP,6TMS,isomer #2	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3259.4	Semi standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #2	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3372.6	Standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #2	C[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3769.5	Standard polar	33892256
8-Oxo-dGMP,6TMS,isomer #3	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3294.7	Semi standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #3	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3168.2	Standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #3	C[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C)N(C1C[C@H](O[Si](C)(C)C)C(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O1)C(=O)N2[Si](C)(C)C	3897.6	Standard polar	33892256
8-Oxo-dGMP,6TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3305.9	Semi standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3331.1	Standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #4	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C	3914.2	Standard polar	33892256
8-Oxo-dGMP,6TMS,isomer #5	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3301.2	Semi standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #5	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3400.7	Standard non polar	33892256
8-Oxo-dGMP,6TMS,isomer #5	C[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C	3859.7	Standard polar	33892256
8-Oxo-dGMP,7TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3372.6	Semi standard non polar	33892256
8-Oxo-dGMP,7TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3282.3	Standard non polar	33892256
8-Oxo-dGMP,7TMS,isomer #1	C[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C)C3=C2N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)OC1COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3632.4	Standard polar	33892256
8-Oxo-dGMP,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O	3390.2	Semi standard non polar	33892256
8-Oxo-dGMP,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)C[C@@H]1O	3415.0	Semi standard non polar	33892256
8-Oxo-dGMP,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	3354.4	Semi standard non polar	33892256
8-Oxo-dGMP,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N1C(N)=NC(=O)C2=C1N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	3379.9	Semi standard non polar	33892256
8-Oxo-dGMP,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N1C(=O)N(C2C[C@H](O)C(COP(=O)(O)O)O2)C2=C1C(=O)N=C(N)[NH]2	3436.0	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	3545.3	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	3685.5	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	5234.9	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3559.4	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3791.6	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	5506.2	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	3555.9	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	3890.8	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2	5465.4	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N1C(N)=NC(=O)C2=C1N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3604.9	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N1C(N)=NC(=O)C2=C1N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3771.7	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N1C(N)=NC(=O)C2=C1N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	5662.1	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	3477.6	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	3789.0	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	5480.0	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O	3579.5	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O	3639.4	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O	5519.7	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	3534.5	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	3759.3	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	5637.3	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	3546.1	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	3707.4	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	5124.4	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3527.3	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3791.0	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	5240.7	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O	3584.5	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O	3669.8	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O	5249.5	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O	3549.3	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O	3783.8	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O	5361.8	Standard polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C(C)(C)C	3506.1	Semi standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C(C)(C)C	3893.8	Standard non polar	33892256
8-Oxo-dGMP,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C(C)(C)C	5436.9	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3654.9	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3778.7	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4848.5	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	3707.5	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	3790.9	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	4863.5	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	3695.9	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	3920.3	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	4986.3	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)C[C@@H]1O	3665.6	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)C[C@@H]1O	4041.9	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)C[C@@H]1O	4821.0	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3756.1	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3914.4	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	4933.1	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3741.4	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	4019.8	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	4885.7	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O	3773.7	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O	3893.3	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O	5140.6	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3774.7	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4053.0	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5010.3	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C(C)(C)C	3734.8	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C(C)(C)C	4152.1	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)[NH]2)[Si](C)(C)C(C)(C)C	5029.7	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3806.6	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	4019.3	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	5131.0	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3689.4	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3906.7	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	4889.5	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	3720.1	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	3739.0	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	4974.1	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	3704.4	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	3875.6	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	5104.1	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)OC1COP(=O)(O)O	3635.7	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)OC1COP(=O)(O)O	4042.7	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)OC1COP(=O)(O)O	4987.8	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3717.6	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3883.1	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	5103.9	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	3702.6	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	3992.1	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)[NH]2	5056.0	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	3774.2	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	3848.8	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O	5363.1	Standard polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3702.5	Semi standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3936.6	Standard non polar	33892256
8-Oxo-dGMP,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	4782.1	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3873.3	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3969.2	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	4507.4	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3967.2	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	4032.7	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C	4755.4	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	3835.5	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	4155.6	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	4421.3	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3936.5	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3986.2	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	4552.5	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3915.9	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	4098.2	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	4503.1	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	3940.7	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	3958.3	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)C[C@@H]1O)O[Si](C)(C)C(C)(C)C	4805.3	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)C[C@@H]1O	3940.9	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)C[C@@H]1O	4127.9	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)C[C@@H]1O	4503.6	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=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=O)C[C@@H]1O	3906.8	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=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=O)C[C@@H]1O	4237.7	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OCC1OC(N2C(=O)[NH]C3=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=O)C[C@@H]1O	4522.6	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3997.8	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	4076.4	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	4647.4	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4004.3	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4223.8	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O)C(COP(=O)(O)O)O1)C(=O)N2[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4715.2	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3850.2	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3775.1	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4645.5	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3872.6	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3914.4	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4764.4	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	3826.9	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	4106.2	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	4471.2	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3934.5	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	3934.6	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)N2[Si](C)(C)C(C)(C)C	4618.9	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	3920.0	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	4039.5	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N1[Si](C)(C)C(C)(C)C)N(C1C[C@H](O[Si](C)(C)C(C)(C)C)C(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O1)C(=O)[NH]2	4564.0	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	3967.3	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	3909.0	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2N([Si](C)(C)C(C)(C)C)C(N)=NC3=O)OC1COP(=O)(O)O[Si](C)(C)C(C)(C)C	4889.9	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)OC1COP(=O)(O)O	3917.3	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)OC1COP(=O)(O)O	4091.6	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)N([Si](C)(C)C(C)(C)C)C3=C2[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)OC1COP(=O)(O)O	4597.7	Standard polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=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=O)OC1COP(=O)(O)O	3876.4	Semi standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=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=O)OC1COP(=O)(O)O	4191.7	Standard non polar	33892256
8-Oxo-dGMP,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1CC(N2C(=O)[NH]C3=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=O)OC1COP(=O)(O)O	4619.2	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Oxo-dGMP GC-MS (Non-derivatized) - 70eV, Positive	splash10-0002-9322000000-a96a87df1eb6a033b2c6	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Oxo-dGMP GC-MS (1 TMS) - 70eV, Positive	splash10-0002-9220100000-a730acbf06167a837d65	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Oxo-dGMP GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Oxo-dGMP 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 - 8-Oxo-dGMP 10V, Positive-QTOF	splash10-014i-0900000000-17afa8db0a103a9d78cf	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 20V, Positive-QTOF	splash10-014i-0900000000-730d6cf8a8af3b2f4896	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 40V, Positive-QTOF	splash10-0gb9-0900000000-75da77bef96bdce1d716	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 10V, Negative-QTOF	splash10-03fr-5209000000-640c16b49b93300fd79f	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 20V, Negative-QTOF	splash10-004i-9400000000-fe0220f3e0d0d30586b0	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 40V, Negative-QTOF	splash10-004i-9100000000-644bcc4b9ebe6d9229a3	2016-09-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 10V, Positive-QTOF	splash10-03xr-0149000000-e56c08bb8b99b0293f4e	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 20V, Positive-QTOF	splash10-014i-0920000000-ccb69db0d7b30b629305	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 40V, Positive-QTOF	splash10-014i-1930000000-a2811cea8c32b84be9f0	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 10V, Negative-QTOF	splash10-03di-1009000000-9f44f66efd9e707294ff	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 20V, Negative-QTOF	splash10-004i-9002000000-d9e3a2dca5a81da5a6de	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Oxo-dGMP 40V, Negative-QTOF	splash10-004i-9100000000-f2e971234f651dc6d224	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB028359

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53481020

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

Hayakawa H, Taketomi A, Sakumi K, Kuwano M, Sekiguchi M: Generation and elimination of 8-oxo-7,8-dihydro-2'-deoxyguanosine 5'-triphosphate, a mutagenic substrate for DNA synthesis, in human cells. Biochemistry. 1995 Jan 10;34(1):89-95. [PubMed:7819228 ]
Kennedy CH, Pass HI, Mitchell JB: Expression of human MutT homologue (hMTH1) protein in primary non-small-cell lung carcinomas and histologically normal surrounding tissue. Free Radic Biol Med. 2003 Jun 1;34(11):1447-57. [PubMed:12757855 ]

Enzymes

Enzyme Details

1. ADP-sugar pyrophosphatase

General function:: Involved in hydrolase activity
Specific function:: Hydrolyzes with similar activities ADP-ribose ADP-mannose, ADP-glucose, 8-oxo-GDP and 8-oxo-dGDP. Can also hydrolyze other nucleotide sugars with low activity.
Gene Name:: NUDT5
Uniprot ID:: Q9UKK9
Molecular weight:: 24327.41

Reactions

8-oxo-dGDP + Water → 8-Oxo-dGMP + Phosphate	details

Enzyme Details

2. 7,8-dihydro-8-oxoguanine triphosphatase

General function:: Involved in 8-oxo-7,8-dihydroguanosine triphosphate pyrophosphatase activity
Specific function:: Antimutagenic. Acts as a sanitizing enzyme for oxidized nucleotide pools, thus suppressing cell dysfunction and death induced by oxidative stress. Hydrolyzes 8-oxo-dGTP, 8-oxo-dATP and 2-OH-dATP, thus preventing misincorporation of oxidized purine nucleoside triphosphates into DNA and subsequently preventing A:T to C:G and G:C to T:A transversions. Able to hydrolyze also the corresponding ribonucleotides, 2-OH-ATP, 8-oxo-GTP and 8-oxo-ATP.
Gene Name:: NUDT1
Uniprot ID:: P36639
Molecular weight:: 17951.435

Reactions

8-Oxo-dGTP + Water → 8-Oxo-dGMP + Pyrophosphate	details

Enzyme Details

3. Probable 8-oxo-dGTP diphosphatase NUDT15

General function:: Involved in hydrolase activity
Specific function:: Mediates the hydrolysis of some nucleoside diphosphate derivatives. Can degrade 8-oxo-dGTP in vitro, suggesting that it may remove an oxidatively damaged form of guanine (7,8-dihydro-8-oxoguanine) from DNA and the nucleotide pool, thereby preventing misincorporation of 8-oxo-dGTP into DNA thus preventing A:T to C:G transversions. Its substrate specificity in vivo however remains unclear (By similarity). May have a role in DNA synthesis and cell cycle progression through the interaction with PCNA.
Gene Name:: NUDT15
Uniprot ID:: Q9NV35
Molecular weight:: 18608.965

Reactions

8-Oxo-dGTP + Water → 8-Oxo-dGMP + Pyrophosphate	details

Enzyme Details

4. 8-oxo-dGDP phosphatase NUDT18

General function:: Involved in hydrolase activity
Specific function:: Mediates the hydrolyzis of oxidized nucleoside diphosphate derivatives. Hydrolyzes 8-oxo-7,8-dihydroguanine (8-oxo-Gua)-containing deoxyribo- and ribonucleoside diphosphates to the monophosphates. Hydrolyzes 8-oxo-dGDP and 8-oxo-GDP with the same efficiencies. Hydrolyzes also 8-OH-dADP and 2-OH-dADP. Exhibited no or minimal hydrolyzis activity against 8-oxo-dGTP, 8-oxo-GTP, dGTP, GTP, dGDP and GDP. Probably removes oxidized guanine nucleotides from both the DNA and RNA precursor pools.
Gene Name:: NUDT18
Uniprot ID:: Q6ZVK8
Molecular weight:: 35500.76

Reactions

8-oxo-dGDP + Water → 8-Oxo-dGMP + Phosphate	details

Showing metabocard for 8-Oxo-dGMP (HMDB0011670)

MOL for HMDB0011670 (8-Oxo-dGMP)

3D MOL for HMDB0011670 (8-Oxo-dGMP)

3D SDF for HMDB0011670 (8-Oxo-dGMP)

3D-SDF for HMDB0011670 (8-Oxo-dGMP)

PDB for HMDB0011670 (8-Oxo-dGMP)

3D PDB for HMDB0011670 (8-Oxo-dGMP)

SMILES for HMDB0011670 (8-Oxo-dGMP)

INCHI for HMDB0011670 (8-Oxo-dGMP)

Structure for HMDB0011670 (8-Oxo-dGMP)

3D Structure for HMDB0011670 (8-Oxo-dGMP)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions

Reactions

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