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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 00:18:06 UTC

Update Date

2021-09-26 22:56:54 UTC

HMDB ID

HMDB0247293

Secondary Accession Numbers

None

Metabolite Identification

Common Name

7,8-Dihydro-2'-deoxyguanosine

Description

7,8-Dihydro-2'-deoxyguanosine belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. Purine 2'-deoxyribonucleosides are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2. Based on a literature review a significant number of articles have been published on 7,8-Dihydro-2'-deoxyguanosine. This compound has been identified in human blood as reported by (PMID: 31557052 ). 7,8-dihydro-2'-deoxyguanosine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 7,8-Dihydro-2'-deoxyguanosine is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0247293
     RDKit          3D
7,8-Dihydro-2'-deoxyguanosine
 34 36  0  0  0  0  0  0  0  0999 V2000
   -3.0694    2.8007    0.4139 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8616    1.4346    0.0262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7385    0.8003    0.3996 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5583   -0.4829    0.0274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5165   -1.1311   -0.7262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6682   -0.4669   -1.1041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5242   -1.0589   -1.7820 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8008    0.8096   -0.7086 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0228   -2.4586   -0.9448 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9286   -2.6876    0.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4487   -1.3555    0.3053 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8843   -0.9696    0.7853 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9470   -1.3766   -0.1774 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8443   -0.1770   -0.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9287   -0.2713    0.6302 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9004    0.9283    0.1792 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    2.0330    0.8373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6000    2.5062   -0.1346 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9742    0.3697    1.0318 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7374    3.1239    1.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5376    3.4570   -0.2092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6663    1.3652   -0.9720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3991   -3.0957   -1.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1871   -3.3089   -0.5217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2958   -3.2268    0.8827 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0786   -1.5056    1.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5139   -1.5067   -1.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4698   -2.3053    0.1150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2225    0.0262   -1.2626 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5882   -0.4693    1.5378 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3783    1.3626   -0.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3233    1.6361    1.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0744    2.8864    1.1284 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5266    2.3146    0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  5  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
  8  2  1  0
 19 12  1  0
 11  4  1  0
  1 20  1  0
  1 21  1  0
  8 22  1  0
  9 23  1  0
 10 24  1  0
 10 25  1  0
 12 26  1  0
 13 27  1  0
 13 28  1  0
 14 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  0
 17 33  1  0
 18 34  1  0
M  END


  Mrv1652309112102182D          

 19 21  0  0  0  0            999 V2000
   -1.1831    1.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831    1.8341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    2.0890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0865    1.4216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.7541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.1271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6955    3.4867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8505    2.3190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  2  0  0  0  0
 12 16  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  0  0  0  0
  2 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0247293

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1

> <INCHI_IDENTIFIER>
InChI=1S/C10H15N5O4/c11-10-13-8-7(9(18)14-10)12-3-15(8)6-1-4(17)5(2-16)19-6/h4-6,12,16-17H,1-3H2,(H3,11,13,14,18)

> <INCHI_KEY>
DYQXERDJEYZBKH-UHFFFAOYSA-N

> <FORMULA>
C10H15N5O4

> <MOLECULAR_WEIGHT>
269.261

> <EXACT_MASS>
269.112403983

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
26.22757671916941

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-amino-9-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-6,7,8,9-tetrahydro-1H-purin-6-one

> <ALOGPS_LOGP>
-2.06

> <JCHEM_LOGP>
-1.8668718433333336

> <ALOGPS_LOGS>
-1.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.895517301259233

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.8142823797146885

> <JCHEM_PKA_STRONGEST_BASIC>
1.7479311160792055

> <JCHEM_POLAR_SURFACE_AREA>
132.44

> <JCHEM_REFRACTIVITY>
72.58269999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.22e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-amino-9-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7,8-dihydro-1H-purin-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0247293
     RDKit          3D
7,8-Dihydro-2'-deoxyguanosine
 34 36  0  0  0  0  0  0  0  0999 V2000
   -3.0694    2.8007    0.4139 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8616    1.4346    0.0262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7385    0.8003    0.3996 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5583   -0.4829    0.0274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5165   -1.1311   -0.7262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6682   -0.4669   -1.1041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5242   -1.0589   -1.7820 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8008    0.8096   -0.7086 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0228   -2.4586   -0.9448 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9286   -2.6876    0.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4487   -1.3555    0.3053 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8843   -0.9696    0.7853 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9470   -1.3766   -0.1774 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8443   -0.1770   -0.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9287   -0.2713    0.6302 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9004    0.9283    0.1792 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    2.0330    0.8373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6000    2.5062   -0.1346 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9742    0.3697    1.0318 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7374    3.1239    1.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5376    3.4570   -0.2092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6663    1.3652   -0.9720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3991   -3.0957   -1.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1871   -3.3089   -0.5217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2958   -3.2268    0.8827 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0786   -1.5056    1.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5139   -1.5067   -1.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4698   -2.3053    0.1150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2225    0.0262   -1.2626 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5882   -0.4693    1.5378 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3783    1.3626   -0.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3233    1.6361    1.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0744    2.8864    1.1284 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5266    2.3146    0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  5  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
  8  2  1  0
 19 12  1  0
 11  4  1  0
  1 20  1  0
  1 21  1  0
  8 22  1  0
  9 23  1  0
 10 24  1  0
 10 25  1  0
 12 26  1  0
 13 27  1  0
 13 28  1  0
 14 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  0
 17 33  1  0
 18 34  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -2.208   1.884   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.208   3.424   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.744   3.899   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.161   2.654   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.744   1.408   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -0.268  -0.057   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -0.268  -2.549   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       2.530   0.237   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       3.864  -0.533   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       3.864  -2.073   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.530  -4.383   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0       5.198   0.237   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -0.268   5.364   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.298   6.509   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -3.454   4.329   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1    3   19                                                  
CONECT    3    2    4   17                                                  
CONECT    4    3    5                                                       
CONECT    5    4    1    6                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9    6   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14                                                            
CONECT   16   12                                                            
CONECT   17    3   18                                                       
CONECT   18   17                                                            
CONECT   19    2                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

COMPND    HMDB0247293
HETATM    1  N1  UNL     1      -3.069   2.801   0.414  1.00  0.00           N  
HETATM    2  C1  UNL     1      -2.862   1.435   0.026  1.00  0.00           C  
HETATM    3  N2  UNL     1      -1.738   0.800   0.400  1.00  0.00           N  
HETATM    4  C2  UNL     1      -1.558  -0.483   0.027  1.00  0.00           C  
HETATM    5  C3  UNL     1      -2.516  -1.131  -0.726  1.00  0.00           C  
HETATM    6  C4  UNL     1      -3.668  -0.467  -1.104  1.00  0.00           C  
HETATM    7  O1  UNL     1      -4.524  -1.059  -1.782  1.00  0.00           O  
HETATM    8  N3  UNL     1      -3.801   0.810  -0.709  1.00  0.00           N  
HETATM    9  N4  UNL     1      -2.023  -2.459  -0.945  1.00  0.00           N  
HETATM   10  C5  UNL     1      -0.929  -2.688   0.011  1.00  0.00           C  
HETATM   11  N5  UNL     1      -0.449  -1.356   0.305  1.00  0.00           N  
HETATM   12  C6  UNL     1       0.884  -0.970   0.785  1.00  0.00           C  
HETATM   13  C7  UNL     1       1.947  -1.377  -0.177  1.00  0.00           C  
HETATM   14  C8  UNL     1       2.844  -0.177  -0.237  1.00  0.00           C  
HETATM   15  O2  UNL     1       3.929  -0.271   0.630  1.00  0.00           O  
HETATM   16  C9  UNL     1       1.900   0.928   0.179  1.00  0.00           C  
HETATM   17  C10 UNL     1       2.706   2.033   0.837  1.00  0.00           C  
HETATM   18  O3  UNL     1       3.600   2.506  -0.135  1.00  0.00           O  
HETATM   19  O4  UNL     1       0.974   0.370   1.032  1.00  0.00           O  
HETATM   20  H1  UNL     1      -2.737   3.124   1.343  1.00  0.00           H  
HETATM   21  H2  UNL     1      -3.538   3.457  -0.209  1.00  0.00           H  
HETATM   22  H3  UNL     1      -4.666   1.365  -0.972  1.00  0.00           H  
HETATM   23  H4  UNL     1      -2.399  -3.096  -1.654  1.00  0.00           H  
HETATM   24  H5  UNL     1      -0.187  -3.309  -0.522  1.00  0.00           H  
HETATM   25  H6  UNL     1      -1.296  -3.227   0.883  1.00  0.00           H  
HETATM   26  H7  UNL     1       1.079  -1.506   1.761  1.00  0.00           H  
HETATM   27  H8  UNL     1       1.514  -1.507  -1.207  1.00  0.00           H  
HETATM   28  H9  UNL     1       2.470  -2.305   0.115  1.00  0.00           H  
HETATM   29  H10 UNL     1       3.222   0.026  -1.263  1.00  0.00           H  
HETATM   30  H11 UNL     1       3.588  -0.469   1.538  1.00  0.00           H  
HETATM   31  H12 UNL     1       1.378   1.363  -0.702  1.00  0.00           H  
HETATM   32  H13 UNL     1       3.323   1.636   1.663  1.00  0.00           H  
HETATM   33  H14 UNL     1       2.074   2.886   1.128  1.00  0.00           H  
HETATM   34  H15 UNL     1       4.527   2.315   0.082  1.00  0.00           H  
CONECT    1    2   20   21
CONECT    2    3    3    8
CONECT    3    4
CONECT    4    5    5   11
CONECT    5    6    9
CONECT    6    7    7    8
CONECT    8   22
CONECT    9   10   23
CONECT   10   11   24   25
CONECT   11   12
CONECT   12   13   19   26
CONECT   13   14   27   28
CONECT   14   15   16   29
CONECT   15   30
CONECT   16   17   19   31
CONECT   17   18   32   33
CONECT   18   34
END

HMDB0247293
     RDKit          3D
7,8-Dihydro-2'-deoxyguanosine
 34 36  0  0  0  0  0  0  0  0999 V2000
   -3.0694    2.8007    0.4139 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8616    1.4346    0.0262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7385    0.8003    0.3996 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5583   -0.4829    0.0274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5165   -1.1311   -0.7262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6682   -0.4669   -1.1041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5242   -1.0589   -1.7820 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8008    0.8096   -0.7086 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0228   -2.4586   -0.9448 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9286   -2.6876    0.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4487   -1.3555    0.3053 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8843   -0.9696    0.7853 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9470   -1.3766   -0.1774 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8443   -0.1770   -0.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9287   -0.2713    0.6302 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9004    0.9283    0.1792 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    2.0330    0.8373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6000    2.5062   -0.1346 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9742    0.3697    1.0318 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7374    3.1239    1.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5376    3.4570   -0.2092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6663    1.3652   -0.9720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3991   -3.0957   -1.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1871   -3.3089   -0.5217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2958   -3.2268    0.8827 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0786   -1.5056    1.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5139   -1.5067   -1.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4698   -2.3053    0.1150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2225    0.0262   -1.2626 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5882   -0.4693    1.5378 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3783    1.3626   -0.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3233    1.6361    1.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0744    2.8864    1.1284 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5266    2.3146    0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  5  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
  8  2  1  0
 19 12  1  0
 11  4  1  0
  1 20  1  0
  1 21  1  0
  8 22  1  0
  9 23  1  0
 10 24  1  0
 10 25  1  0
 12 26  1  0
 13 27  1  0
 13 28  1  0
 14 29  1  0
 15 30  1  0
 16 31  1  0
 17 32  1  0
 17 33  1  0
 18 34  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₀H₁₅N₅O₄

Average Molecular Weight

269.261

Monoisotopic Molecular Weight

269.112403983

IUPAC Name

2-amino-9-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-6,7,8,9-tetrahydro-1H-purin-6-one

Traditional Name

2-amino-9-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7,8-dihydro-1H-purin-6-one

CAS Registry Number

Not Available

SMILES

NC1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1

InChI Identifier

InChI=1S/C10H15N5O4/c11-10-13-8-7(9(18)14-10)12-3-15(8)6-1-4(17)5(2-16)19-6/h4-6,12,16-17H,1-3H2,(H3,11,13,14,18)

InChI Key

DYQXERDJEYZBKH-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. Purine 2'-deoxyribonucleosides are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Sub Class

Purine 2'-deoxyribonucleosides

Direct Parent

Purine 2'-deoxyribonucleosides

Alternative Parents

Substituents

Purine 2'-deoxyribonucleoside
Pentose monosaccharide
Purinone
Imidazopyrimidine
Purine
Dialkylarylamine
Aminopyrimidine
Pyrimidone
Monosaccharide
Pyrimidine
Oxolane
Heteroaromatic compound
Vinylogous amide
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Primary alcohol
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
Primary amine
Amine
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-2.1	ALOGPS
logP	-1.9	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	7.81	ChemAxon
pKa (Strongest Basic)	1.75	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	132.44 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	72.58 m³·mol⁻¹	ChemAxon
Polarizability	26.23 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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
DeepCCS	[M+H]+	157.764	30932474
DeepCCS	[M-H]-	155.406	30932474
DeepCCS	[M-2H]-	188.372	30932474
DeepCCS	[M+Na]+	163.858	30932474
AllCCS	[M+H]+	161.2	32859911
AllCCS	[M+H-H2O]+	157.6	32859911
AllCCS	[M+NH4]+	164.5	32859911
AllCCS	[M+Na]+	165.5	32859911
AllCCS	[M-H]-	160.5	32859911
AllCCS	[M+Na-2H]-	160.1	32859911
AllCCS	[M+HCOO]-	159.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
7,8-Dihydro-2'-deoxyguanosine	NC1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1	3692.1	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine	NC1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1	2714.2	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine	NC1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1	3113.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O2)C(=O)[NH]1	2829.5	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O2)C(=O)[NH]1	2812.1	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O2)C(=O)[NH]1	5188.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C)O1	2725.2	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C)O1	2900.1	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C)O1	4075.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #11	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N)N([Si](C)(C)C)C3=O)CC1O	2774.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #11	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N)N([Si](C)(C)C)C3=O)CC1O	2886.6	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #11	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N)N([Si](C)(C)C)C3=O)CC1O	4048.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #12	C[Si](C)(C)N(C1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1[Si](C)(C)C)[Si](C)(C)C	2941.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #12	C[Si](C)(C)N(C1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1[Si](C)(C)C)[Si](C)(C)C	3011.7	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #12	C[Si](C)(C)N(C1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1[Si](C)(C)C)[Si](C)(C)C	5000.0	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #13	C[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2782.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #13	C[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	3042.0	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #13	C[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4021.4	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O)C(CO)O1	2820.1	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O)C(CO)O1	2967.2	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #14	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O)C(CO)O1	4078.4	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #2	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N)[NH]C3=O)CC1O[Si](C)(C)C	2679.4	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #2	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N)[NH]C3=O)CC1O[Si](C)(C)C	2770.2	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #2	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N)[NH]C3=O)CC1O[Si](C)(C)C	3856.7	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #3	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	2851.0	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #3	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	2764.1	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #3	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	4461.8	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #4	C[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)OC1CO	2912.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #4	C[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)OC1CO	2910.1	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #4	C[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)OC1CO	5151.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C)C(CO)O2)C(=O)N1[Si](C)(C)C	2888.4	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C)C(CO)O2)C(=O)N1[Si](C)(C)C	2867.6	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #5	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C)C(CO)O2)C(=O)N1[Si](C)(C)C	4912.3	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO)O1	2740.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO)O1	2845.3	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO)O1	4032.4	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #7	C[Si](C)(C)OC1CC(N2CN([Si](C)(C)C)C3=C2N=C(N)N([Si](C)(C)C)C3=O)OC1CO	2784.0	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #7	C[Si](C)(C)OC1CC(N2CN([Si](C)(C)C)C3=C2N=C(N)N([Si](C)(C)C)C3=O)OC1CO	2827.3	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #7	C[Si](C)(C)OC1CC(N2CN([Si](C)(C)C)C3=C2N=C(N)N([Si](C)(C)C)C3=O)OC1CO	4018.5	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #8	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O	2900.2	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #8	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O	2960.8	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #8	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O	5182.9	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O)C(CO[Si](C)(C)C)O2)C(=O)N1[Si](C)(C)C	2877.2	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O)C(CO[Si](C)(C)C)O2)C(=O)N1[Si](C)(C)C	2923.3	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TMS,isomer #9	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O)C(CO[Si](C)(C)C)O2)C(=O)N1[Si](C)(C)C	4951.7	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #1	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C	2871.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #1	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C	2911.7	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #1	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C	4894.5	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C)O1	2800.2	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C)O1	2972.3	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #10	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C)O1	3730.7	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #11	C[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2871.3	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #11	C[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	3124.3	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #11	C[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	3720.0	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O2)C(=O)N1[Si](C)(C)C	2860.4	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O2)C(=O)N1[Si](C)(C)C	2847.1	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O2)C(=O)N1[Si](C)(C)C	4631.1	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #3	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O1	2712.6	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #3	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O1	2825.1	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #3	C[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O1	3674.3	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #4	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	2779.4	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #4	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	2831.7	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #4	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	3798.9	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #5	C[Si](C)(C)OC1CC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)OC1CO	2788.2	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #5	C[Si](C)(C)OC1CC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)OC1CO	3002.9	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #5	C[Si](C)(C)OC1CC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)OC1CO	3620.7	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #6	C[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)OC1CO	2933.6	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #6	C[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)OC1CO	2991.0	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #6	C[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)OC1CO	4593.6	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #7	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO)O1	2812.7	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #7	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO)O1	2922.4	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #7	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO)O1	3684.3	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #8	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O	2785.7	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #8	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O	3045.9	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #8	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O	3667.4	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #9	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O	2921.0	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #9	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O	3038.8	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TMS,isomer #9	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O	4631.3	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #1	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C	2804.4	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #1	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C	2955.1	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #1	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C	3332.5	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #2	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	2942.3	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #2	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	2973.3	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #2	C[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	4343.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #3	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O1	2824.0	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #3	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O1	2895.8	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #3	C[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N([Si](C)(C)C)CN2C1CC(O[Si](C)(C)C)C(CO[Si](C)(C)C)O1	3393.8	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #4	C[Si](C)(C)OC1CC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)OC1CO	2889.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #4	C[Si](C)(C)OC1CC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)OC1CO	3078.5	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #4	C[Si](C)(C)OC1CC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)OC1CO	3371.6	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #5	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O	2881.1	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #5	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O	3118.2	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TMS,isomer #5	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O	3421.6	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,6TMS,isomer #1	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	2916.9	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,6TMS,isomer #1	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	3043.5	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,6TMS,isomer #1	C[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C)C3=C2N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C3=O)CC1O[Si](C)(C)C	3116.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]1	3449.5	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]1	3425.9	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]1	5156.8	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C(C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C(C)(C)C)O1	3329.5	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C(C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C(C)(C)C)O1	3622.4	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C(C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C(C)(C)C)O1	4126.5	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)CC1O	3426.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)CC1O	3611.6	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)CC1O	4074.7	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N(C1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3522.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N(C1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3634.0	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N(C1=NC2=C(NCN2C2CC(O)C(CO)O2)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4768.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3367.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3751.3	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4030.9	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O)C(CO)O1	3451.6	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O)C(CO)O1	3705.4	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O)C(CO)O1	4059.9	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)[NH]C3=O)CC1O[Si](C)(C)C(C)(C)C	3290.0	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)[NH]C3=O)CC1O[Si](C)(C)C(C)(C)C	3488.0	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)[NH]C3=O)CC1O[Si](C)(C)C(C)(C)C	3926.1	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)CC1O[Si](C)(C)C(C)(C)C	3516.0	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)CC1O[Si](C)(C)C(C)(C)C	3400.4	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)CC1O[Si](C)(C)C(C)(C)C	4384.9	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)OC1CO	3455.0	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)OC1CO	3505.5	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)OC1CO	5068.6	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C(C)(C)C)C(CO)O2)C(=O)N1[Si](C)(C)C(C)(C)C	3543.4	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C(C)(C)C)C(CO)O2)C(=O)N1[Si](C)(C)C(C)(C)C	3497.5	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C(C)(C)C)C(CO)O2)C(=O)N1[Si](C)(C)C(C)(C)C	4787.3	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO)O1	3321.9	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO)O1	3567.2	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO)O1	4076.4	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1CC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)OC1CO	3428.0	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1CC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)OC1CO	3541.9	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1CC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)OC1CO	4034.5	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O	3451.2	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O	3554.4	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O	5107.1	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O)C(CO[Si](C)(C)C(C)(C)C)O2)C(=O)N1[Si](C)(C)C(C)(C)C	3538.3	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O)C(CO[Si](C)(C)C(C)(C)C)O2)C(=O)N1[Si](C)(C)C(C)(C)C	3548.3	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O)C(CO[Si](C)(C)C(C)(C)C)O2)C(=O)N1[Si](C)(C)C(C)(C)C	4827.1	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C(C)(C)C	3625.2	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C(C)(C)C	3669.6	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C(C)(C)C	4877.0	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C(C)(C)C)O1	3620.4	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C(C)(C)C)O1	3885.1	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O)C(CO[Si](C)(C)C(C)(C)C)O1	3862.3	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3644.7	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4020.5	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N1CN(C2CC(O)C(CO)O2)C2=C1C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3835.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O2)C(=O)N1[Si](C)(C)C(C)(C)C	3699.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O2)C(=O)N1[Si](C)(C)C(C)(C)C	3650.6	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(NCN2C2CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O2)C(=O)N1[Si](C)(C)C(C)(C)C	4564.4	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O1	3476.5	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O1	3734.2	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O1	3873.0	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)CC1O[Si](C)(C)C(C)(C)C	3596.6	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)CC1O[Si](C)(C)C(C)(C)C	3717.3	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N)N([Si](C)(C)C(C)(C)C)C3=O)CC1O[Si](C)(C)C(C)(C)C	3926.6	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1CC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)OC1CO	3520.1	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1CC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)OC1CO	3879.9	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1CC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)OC1CO	3782.8	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)OC1CO	3709.5	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)OC1CO	3764.5	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1CC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)OC1CO	4484.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO)O1	3608.8	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO)O1	3817.6	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO)O1	3818.9	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O	3535.1	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O	3945.6	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O	3827.0	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)CC1O	3715.4	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)CC1O	3818.2	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)CC1O	4529.2	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C(C)(C)C	3666.1	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C(C)(C)C	3993.8	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C3=O)CC1O[Si](C)(C)C(C)(C)C	3646.6	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)CC1O[Si](C)(C)C(C)(C)C	3872.5	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)CC1O[Si](C)(C)C(C)(C)C	3891.6	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(N2CNC3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)CC1O[Si](C)(C)C(C)(C)C	4335.9	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O1	3754.9	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O1	3933.8	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)CN2C1CC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)O1	3710.6	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1CC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)OC1CO	3796.6	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1CC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)OC1CO	4076.9	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1CC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)OC1CO	3636.0	Standard polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)CC1O	3818.5	Semi standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)CC1O	4141.5	Standard non polar	33892256
7,8-Dihydro-2'-deoxyguanosine,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(N2CN([Si](C)(C)C(C)(C)C)C3=C2N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C3=O)CC1O	3682.2	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-8590000000-0a46254ec2192b54b603	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TBDMS_1_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TBDMS_1_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-03	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 - 7,8-Dihydro-2'-deoxyguanosine 10V, Positive-QTOF	splash10-0udi-0900000000-42cdd828a6c4e37d7d70	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine 20V, Positive-QTOF	splash10-0udi-0900000000-42cdd828a6c4e37d7d70	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine 40V, Positive-QTOF	splash10-0udr-0900000000-c2d754b1b965629c967e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine 10V, Negative-QTOF	splash10-0gb9-0490000000-4a5f3eb74355cc032f77	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine 20V, Negative-QTOF	splash10-0udi-0910000000-1bc597cd4ca778168eca	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 7,8-Dihydro-2'-deoxyguanosine 40V, Negative-QTOF	splash10-000i-2900000000-d6d41d9b2186dc1925f4	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90295342

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 7,8-Dihydro-2'-deoxyguanosine (HMDB0247293)

MOL for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

3D MOL for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

3D SDF for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

3D-SDF for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

PDB for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

3D PDB for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

SMILES for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

INCHI for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

Structure for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

3D Structure for HMDB0247293 (7,8-Dihydro-2'-deoxyguanosine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra