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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 00:34:39 UTC

Update Date

2021-09-26 22:57:20 UTC

HMDB ID

HMDB0247573

Secondary Accession Numbers

None

Metabolite Identification

Common Name

9-(3,4-Dihydroxybutyl)guanine

Description

9-(3,4-Dihydroxybutyl)guanine belongs to the class of organic compounds known as hypoxanthines. Hypoxanthines are compounds containing the purine derivative 1H-purin-6(9H)-one. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring. Based on a literature review a significant number of articles have been published on 9-(3,4-Dihydroxybutyl)guanine. This compound has been identified in human blood as reported by (PMID: 31557052 ). 9-(3,4-dihydroxybutyl)guanine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 9-(3,4-Dihydroxybutyl)guanine 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

HMDB0247573
     RDKit          3D
9-(3,4-Dihydroxybutyl)guanine
 30 31  0  0  0  0  0  0  0  0999 V2000
    3.5708    2.2827   -0.1605 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1406    0.9384   -0.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8785    0.5767   -0.4224 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966   -0.7022   -0.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4152   -1.6792   -0.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7465   -2.8376   -0.1510 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4693   -2.5798   -0.4861 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2884   -1.2644   -0.6473 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9024   -0.5557   -1.0014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7207   -0.1457    0.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9330    0.5852   -0.3202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6222   -0.3117   -1.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8390    1.0577    0.7948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1092    1.9530    1.5937 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7152   -1.3108    0.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5719   -2.1873    0.4818 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0340    0.0002    0.1557 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5140    2.8270   -1.0339 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9382    2.7072    0.7047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3183   -3.3125   -0.6134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5880   -1.1251   -1.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828    0.4046   -1.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9912   -1.0127    0.8394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1026    0.5741    0.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5482    1.4277   -0.9280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6688   -1.1695   -0.6296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2220    0.2102    1.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6687    1.6315    0.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8743    2.7422    1.0807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0123    0.2755    0.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
  5 15  1  0
 15 16  2  0
 15 17  1  0
 17  2  1  0
  8  4  1  0
  1 18  1  0
  1 19  1  0
  7 20  1  0
  9 21  1  0
  9 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 12 26  1  0
 13 27  1  0
 13 28  1  0
 14 29  1  0
 17 30  1  0
M  END

  Mrv1652309112102342D          

 17 18  0  0  0  0            999 V2000
   -3.4873   -0.1731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2942   -0.0016    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7067   -0.7161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1547   -1.3292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4010   -0.9936    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6866   -1.4061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9721   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2576   -1.4061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5432   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1713   -1.4061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2576   -2.2311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4097   -2.1138    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2166   -2.2853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7687   -1.6722    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5137   -0.8876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0658   -0.2745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4716   -3.0699    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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  1  0  0  0  0
  8 11  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  3 15  1  0  0  0  0
 15 16  2  0  0  0  0
 13 17  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0247573

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=NC2=C(N=CN2CCC(O)CO)C(=O)N1

> <INCHI_IDENTIFIER>
InChI=1S/C9H13N5O3/c10-9-12-7-6(8(17)13-9)11-4-14(7)2-1-5(16)3-15/h4-5,15-16H,1-3H2,(H3,10,12,13,17)

> <INCHI_KEY>
QOVUZUCXPAZXDZ-UHFFFAOYSA-N

> <FORMULA>
C9H13N5O3

> <MOLECULAR_WEIGHT>
239.235

> <EXACT_MASS>
239.101839299

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
23.264172041507358

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-amino-9-(3,4-dihydroxybutyl)-6,9-dihydro-1H-purin-6-one

> <ALOGPS_LOGP>
-1.42

> <JCHEM_LOGP>
-2.183068203666667

> <ALOGPS_LOGS>
-1.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.23548221352845

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.169965300186773

> <JCHEM_PKA_STRONGEST_BASIC>
0.6977668557158461

> <JCHEM_POLAR_SURFACE_AREA>
125.76

> <JCHEM_REFRACTIVITY>
60.04169999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.43e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-amino-9-(3,4-dihydroxybutyl)-1H-purin-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0247573
     RDKit          3D
9-(3,4-Dihydroxybutyl)guanine
 30 31  0  0  0  0  0  0  0  0999 V2000
    3.5708    2.2827   -0.1605 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1406    0.9384   -0.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8785    0.5767   -0.4224 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966   -0.7022   -0.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4152   -1.6792   -0.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7465   -2.8376   -0.1510 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4693   -2.5798   -0.4861 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2884   -1.2644   -0.6473 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9024   -0.5557   -1.0014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7207   -0.1457    0.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9330    0.5852   -0.3202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6222   -0.3117   -1.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8390    1.0577    0.7948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1092    1.9530    1.5937 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7152   -1.3108    0.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5719   -2.1873    0.4818 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0340    0.0002    0.1557 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5140    2.8270   -1.0339 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9382    2.7072    0.7047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3183   -3.3125   -0.6134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5880   -1.1251   -1.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828    0.4046   -1.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9912   -1.0127    0.8394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1026    0.5741    0.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5482    1.4277   -0.9280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6688   -1.1695   -0.6296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2220    0.2102    1.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6687    1.6315    0.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8743    2.7422    1.0807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0123    0.2755    0.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
  5 15  1  0
 15 16  2  0
 15 17  1  0
 17  2  1  0
  8  4  1  0
  1 18  1  0
  1 19  1  0
  7 20  1  0
  9 21  1  0
  9 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 12 26  1  0
 13 27  1  0
 13 28  1  0
 14 29  1  0
 17 30  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      -6.510  -0.323   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      -8.016  -0.003   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      -8.786  -1.337   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.755  -2.481   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      -6.349  -1.855   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -5.015  -2.625   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.681  -1.855   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.348  -2.625   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.014  -1.855   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.320  -2.625   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -2.348  -4.165   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0      -8.231  -3.946   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      -9.738  -4.266   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0     -10.768  -3.121   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0     -10.292  -1.657   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0     -11.323  -0.512   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0     -10.214  -5.731   0.000  0.00  0.00           N+0
CONECT    1    2    5                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   15                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8                                                            
CONECT   12    4   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14    3   16                                                  
CONECT   16   15                                                            
CONECT   17   13                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

COMPND    HMDB0247573
HETATM    1  N1  UNL     1       3.571   2.283  -0.161  1.00  0.00           N  
HETATM    2  C1  UNL     1       3.141   0.938  -0.146  1.00  0.00           C  
HETATM    3  N2  UNL     1       1.878   0.577  -0.422  1.00  0.00           N  
HETATM    4  C2  UNL     1       1.497  -0.702  -0.402  1.00  0.00           C  
HETATM    5  C3  UNL     1       2.415  -1.679  -0.091  1.00  0.00           C  
HETATM    6  N3  UNL     1       1.747  -2.838  -0.151  1.00  0.00           N  
HETATM    7  C4  UNL     1       0.469  -2.580  -0.486  1.00  0.00           C  
HETATM    8  N4  UNL     1       0.288  -1.264  -0.647  1.00  0.00           N  
HETATM    9  C5  UNL     1      -0.902  -0.556  -1.001  1.00  0.00           C  
HETATM   10  C6  UNL     1      -1.721  -0.146   0.217  1.00  0.00           C  
HETATM   11  C7  UNL     1      -2.933   0.585  -0.320  1.00  0.00           C  
HETATM   12  O1  UNL     1      -3.622  -0.312  -1.143  1.00  0.00           O  
HETATM   13  C8  UNL     1      -3.839   1.058   0.795  1.00  0.00           C  
HETATM   14  O2  UNL     1      -3.109   1.953   1.594  1.00  0.00           O  
HETATM   15  C9  UNL     1       3.715  -1.311   0.194  1.00  0.00           C  
HETATM   16  O3  UNL     1       4.572  -2.187   0.482  1.00  0.00           O  
HETATM   17  N5  UNL     1       4.034   0.000   0.156  1.00  0.00           N  
HETATM   18  H1  UNL     1       3.514   2.827  -1.034  1.00  0.00           H  
HETATM   19  H2  UNL     1       3.938   2.707   0.705  1.00  0.00           H  
HETATM   20  H3  UNL     1      -0.318  -3.312  -0.613  1.00  0.00           H  
HETATM   21  H4  UNL     1      -1.588  -1.125  -1.654  1.00  0.00           H  
HETATM   22  H5  UNL     1      -0.683   0.405  -1.549  1.00  0.00           H  
HETATM   23  H6  UNL     1      -1.991  -1.013   0.839  1.00  0.00           H  
HETATM   24  H7  UNL     1      -1.103   0.574   0.799  1.00  0.00           H  
HETATM   25  H8  UNL     1      -2.548   1.428  -0.928  1.00  0.00           H  
HETATM   26  H9  UNL     1      -3.669  -1.169  -0.630  1.00  0.00           H  
HETATM   27  H10 UNL     1      -4.222   0.210   1.363  1.00  0.00           H  
HETATM   28  H11 UNL     1      -4.669   1.632   0.336  1.00  0.00           H  
HETATM   29  H12 UNL     1      -2.874   2.742   1.081  1.00  0.00           H  
HETATM   30  H13 UNL     1       5.012   0.276   0.370  1.00  0.00           H  
CONECT    1    2   18   19
CONECT    2    3    3   17
CONECT    3    4
CONECT    4    5    5    8
CONECT    5    6   15
CONECT    6    7    7
CONECT    7    8   20
CONECT    8    9
CONECT    9   10   21   22
CONECT   10   11   23   24
CONECT   11   12   13   25
CONECT   12   26
CONECT   13   14   27   28
CONECT   14   29
CONECT   15   16   16   17
CONECT   17   30
END

HMDB0247573
     RDKit          3D
9-(3,4-Dihydroxybutyl)guanine
 30 31  0  0  0  0  0  0  0  0999 V2000
    3.5708    2.2827   -0.1605 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1406    0.9384   -0.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8785    0.5767   -0.4224 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966   -0.7022   -0.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4152   -1.6792   -0.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7465   -2.8376   -0.1510 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4693   -2.5798   -0.4861 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2884   -1.2644   -0.6473 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9024   -0.5557   -1.0014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7207   -0.1457    0.2174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9330    0.5852   -0.3202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6222   -0.3117   -1.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8390    1.0577    0.7948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1092    1.9530    1.5937 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7152   -1.3108    0.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5719   -2.1873    0.4818 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0340    0.0002    0.1557 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5140    2.8270   -1.0339 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9382    2.7072    0.7047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3183   -3.3125   -0.6134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5880   -1.1251   -1.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828    0.4046   -1.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9912   -1.0127    0.8394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1026    0.5741    0.7995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5482    1.4277   -0.9280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6688   -1.1695   -0.6296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2220    0.2102    1.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6687    1.6315    0.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8743    2.7422    1.0807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0123    0.2755    0.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
  5 15  1  0
 15 16  2  0
 15 17  1  0
 17  2  1  0
  8  4  1  0
  1 18  1  0
  1 19  1  0
  7 20  1  0
  9 21  1  0
  9 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 12 26  1  0
 13 27  1  0
 13 28  1  0
 14 29  1  0
 17 30  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₉H₁₃N₅O₃

Average Molecular Weight

239.235

Monoisotopic Molecular Weight

239.101839299

IUPAC Name

2-amino-9-(3,4-dihydroxybutyl)-6,9-dihydro-1H-purin-6-one

Traditional Name

2-amino-9-(3,4-dihydroxybutyl)-1H-purin-6-one

CAS Registry Number

Not Available

SMILES

NC1=NC2=C(N=CN2CCC(O)CO)C(=O)N1

InChI Identifier

InChI=1S/C9H13N5O3/c10-9-12-7-6(8(17)13-9)11-4-14(7)2-1-5(16)3-15/h4-5,15-16H,1-3H2,(H3,10,12,13,17)

InChI Key

QOVUZUCXPAZXDZ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hypoxanthines. Hypoxanthines are compounds containing the purine derivative 1H-purin-6(9H)-one. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Imidazopyrimidines

Sub Class

Purines and purine derivatives

Direct Parent

Hypoxanthines

Alternative Parents

Substituents

Hypoxanthine
6-oxopurine
Pyrimidone
Aminopyrimidine
Pyrimidine
N-substituted imidazole
Heteroaromatic compound
Vinylogous amide
Imidazole
Azole
Secondary alcohol
1,2-diol
Azacycle
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Primary alcohol
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
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)

Source

Exogenous

Exogenous (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	-1.4	ALOGPS
logP	-2.2	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	10.17	ChemAxon
pKa (Strongest Basic)	0.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	125.76 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	60.04 m³·mol⁻¹	ChemAxon
Polarizability	23.26 Å³	ChemAxon
Number of Rings	2	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]+	149.31	30932474
DeepCCS	[M-H]-	146.952	30932474
DeepCCS	[M-2H]-	181.85	30932474
DeepCCS	[M+Na]+	157.444	30932474
AllCCS	[M+H]+	152.4	32859911
AllCCS	[M+H-H2O]+	148.8	32859911
AllCCS	[M+NH4]+	155.8	32859911
AllCCS	[M+Na]+	156.8	32859911
AllCCS	[M-H]-	153.0	32859911
AllCCS	[M+Na-2H]-	152.9	32859911
AllCCS	[M+HCOO]-	153.0	32859911

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
9-(3,4-Dihydroxybutyl)guanine,1TMS,isomer #1	C[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N)[NH]C2=O	2488.7	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TMS,isomer #1	C[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N)[NH]C2=O	2570.8	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TMS,isomer #1	C[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N)[NH]C2=O	4229.4	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TMS,isomer #4	C[Si](C)(C)N1C(N)=NC2=C(N=CN2CCC(O)CO)C1=O	2616.3	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TMS,isomer #4	C[Si](C)(C)N1C(N)=NC2=C(N=CN2CCC(O)CO)C1=O	2615.3	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TMS,isomer #4	C[Si](C)(C)N1C(N)=NC2=C(N=CN2CCC(O)CO)C1=O	4404.4	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,2TMS,isomer #5	C[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	2538.0	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,2TMS,isomer #5	C[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	2616.4	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,2TMS,isomer #5	C[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O	3921.7	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C)O[Si](C)(C)C)C(=O)[NH]1	2456.1	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C)O[Si](C)(C)C)C(=O)[NH]1	2719.7	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #1	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C)O[Si](C)(C)C)C(=O)[NH]1	3613.2	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #2	C[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O)O[Si](C)(C)C	2502.0	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #2	C[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O)O[Si](C)(C)C	2647.0	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #2	C[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N)N([Si](C)(C)C)C2=O)O[Si](C)(C)C	3715.7	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #3	C[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	2479.2	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #3	C[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	2831.8	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #3	C[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	3512.3	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO)O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	2563.7	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO)O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	2767.1	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #4	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO)O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3566.5	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #5	C[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	2472.0	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #5	C[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	2839.7	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #5	C[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O	3486.7	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(O)CO[Si](C)(C)C)C(=O)N1[Si](C)(C)C	2555.3	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(O)CO[Si](C)(C)C)C(=O)N1[Si](C)(C)C	2763.3	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #6	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(O)CO[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3545.0	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #7	C[Si](C)(C)N(C1=NC2=C(N=CN2CCC(O)CO)C(=O)N1[Si](C)(C)C)[Si](C)(C)C	2614.0	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #7	C[Si](C)(C)N(C1=NC2=C(N=CN2CCC(O)CO)C(=O)N1[Si](C)(C)C)[Si](C)(C)C	2866.7	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TMS,isomer #7	C[Si](C)(C)N(C1=NC2=C(N=CN2CCC(O)CO)C(=O)N1[Si](C)(C)C)[Si](C)(C)C	3553.3	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #1	C[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)O[Si](C)(C)C	2501.7	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #1	C[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)O[Si](C)(C)C	2801.1	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #1	C[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=O)O[Si](C)(C)C	3212.7	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C)O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	2558.4	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C)O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	2732.4	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #2	C[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C)O[Si](C)(C)C)C(=O)N1[Si](C)(C)C	3272.6	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #3	C[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	2604.6	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #3	C[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	2883.3	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #3	C[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	3192.9	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #4	C[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	2585.1	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #4	C[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	2884.1	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TMS,isomer #4	C[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O	3172.5	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,5TMS,isomer #1	C[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)O[Si](C)(C)C	2609.0	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,5TMS,isomer #1	C[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)O[Si](C)(C)C	2856.4	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,5TMS,isomer #1	C[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)C2=O)O[Si](C)(C)C	2960.8	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N)[NH]C2=O	2737.3	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N)[NH]C2=O	2786.2	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N)[NH]C2=O	4206.0	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(O)CO)C(=O)[NH]1	2852.2	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(O)CO)C(=O)[NH]1	2942.1	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(O)CO)C(=O)[NH]1	4319.4	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N)[NH]C2=O)O[Si](C)(C)C(C)(C)C	2899.7	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N)[NH]C2=O)O[Si](C)(C)C(C)(C)C	3095.9	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N)[NH]C2=O)O[Si](C)(C)C(C)(C)C	3813.4	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO)O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	2930.5	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO)O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3185.2	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO)O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3897.4	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3102.3	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3380.2	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)[NH]1	3660.4	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C	3166.5	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C	3333.7	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N)N([Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C	3727.7	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	3083.9	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	3464.6	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	3540.4	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO)O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3170.2	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO)O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3415.7	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO)O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3569.7	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	3070.8	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	3471.4	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O	3534.3	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(O)CO[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3188.4	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(O)CO[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3413.9	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(O)CO[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3563.7	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N(C1=NC2=C(N=CN2CCC(O)CO)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3232.4	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N(C1=NC2=C(N=CN2CCC(O)CO)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3442.9	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N(C1=NC2=C(N=CN2CCC(O)CO)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3530.1	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O)O[Si](C)(C)C(C)(C)C	3255.0	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O)O[Si](C)(C)C(C)(C)C	3636.4	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C2=O)O[Si](C)(C)C(C)(C)C	3426.1	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3343.1	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3581.4	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC1=NC2=C(N=CN2CCC(CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C	3460.9	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O	3356.1	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O	3663.4	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(CO)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O	3392.8	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O	3339.3	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O	3662.2	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC(O)CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O	3389.2	Standard polar	33892256
9-(3,4-Dihydroxybutyl)guanine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C	3516.7	Semi standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C	3788.5	Standard non polar	33892256
9-(3,4-Dihydroxybutyl)guanine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(CCN1C=NC2=C1N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C	3311.7	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (Non-derivatized) - 70eV, Positive	splash10-08nc-6940000000-f6c2b4e076be5c1681f3	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TBDMS_1_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TBDMS_2_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TBDMS_2_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TBDMS_2_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine GC-MS (TBDMS_2_7) - 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 - 9-(3,4-Dihydroxybutyl)guanine 10V, Positive-QTOF	splash10-0006-0390000000-ceeff4b9ebd2207b2075	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine 20V, Positive-QTOF	splash10-0006-0390000000-57ceb495592326c579b7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine 40V, Positive-QTOF	splash10-000i-1900000000-97a0381360f0ad4c689f	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine 10V, Negative-QTOF	splash10-000i-0390000000-8e61fc81a1475c17fcf7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine 20V, Negative-QTOF	splash10-0udj-0930000000-82a15e861b0dd7b563bc	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9-(3,4-Dihydroxybutyl)guanine 40V, Negative-QTOF	splash10-053u-4900000000-3987a54ecd5d5b2786b7	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	¹³C NMR Spectrum (1D, 1000 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	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	¹H NMR Spectrum (1D, 400 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	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	¹H NMR Spectrum (1D, 600 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	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	¹³C NMR Spectrum (1D, 800 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, 900 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

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

113931

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

128542

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 9-(3,4-Dihydroxybutyl)guanine (HMDB0247573)

MOL for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

3D MOL for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

3D SDF for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

3D-SDF for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

PDB for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

3D PDB for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

SMILES for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

INCHI for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

Structure for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

3D Structure for HMDB0247573 (9-(3,4-Dihydroxybutyl)guanine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra