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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 20:54:13 UTC

Update Date

2021-09-26 23:16:17 UTC

HMDB ID

HMDB0259006

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Thiochrome

Description

Thiochrome belongs to the class of organic compounds known as pyrimidines and pyrimidine derivatives. Pyrimidines and pyrimidine derivatives are compounds containing a pyrimidne ring, which is a six-member aromatic heterocycle which consists of two nitrogen atoms (at positions 1 and 3) and four carbon atoms. Based on a literature review very few articles have been published on Thiochrome. This compound has been identified in human blood as reported by (PMID: 31557052 ). Thiochrome is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Thiochrome 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

HMDB0259006
     RDKit          3D
Thiochrome
 32 34  0  0  0  0  0  0  0  0999 V2000
   -2.4132   -1.7338    0.5573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7104   -0.6191   -0.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4217    0.1325   -1.0099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8912    0.0678   -1.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4667    1.4205   -0.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2415    1.6673    0.4706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3523    1.3325   -1.7787 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.1312    0.7237   -0.9331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3442    1.1523   -1.0186 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3454    0.5051   -0.2498 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6415    0.9197   -0.3043 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6129    0.3421    0.3998 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0128    0.8075    0.3261 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2778   -0.6816    1.1826 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0300   -1.1437    1.2878 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9885   -0.5484    0.5530 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6358   -1.0847    0.6965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3336   -0.3403   -0.1456 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1463   -2.2339   -0.0956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6982   -2.5065    0.8757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9340   -1.3381    1.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1120   -0.1349   -2.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3702   -0.7110   -0.6614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0149    2.2436   -1.4552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5477    1.3795   -1.1081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2405    2.6160    0.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4651    0.9494    1.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0670    1.8209   -0.1628 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6409    0.1391   -0.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7882   -1.9787    1.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3487   -0.9956    1.7721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5645   -2.1693    0.4292 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  1  0
  5  6  1  0
  3  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18  2  1  0
 18  8  1  0
 16 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
 13 27  1  0
 13 28  1  0
 13 29  1  0
 15 30  1  0
 17 31  1  0
 17 32  1  0
M  END


  Mrv1533004171515412D          

 18 20  0  0  0  0            999 V2000
    1.5983   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5433   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1308   -2.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6942   -2.6499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -1.2680    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.1104    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.3479    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  3  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  2 18  1  0  0  0  0
  8 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0259006

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=C(CCO)SC2=NC3=NC(C)=NC=C3CN12

> <INCHI_IDENTIFIER>
InChI=1S/C12H14N4OS/c1-7-10(3-4-17)18-12-15-11-9(6-16(7)12)5-13-8(2)14-11/h5,17H,3-4,6H2,1-2H3

> <INCHI_KEY>
GTQXMAIXVFLYKF-UHFFFAOYSA-N

> <FORMULA>
C12H14N4OS

> <MOLECULAR_WEIGHT>
262.33

> <EXACT_MASS>
262.088832261

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
28.165980747086508

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{6,12-dimethyl-4-thia-2,7,11,13-tetraazatricyclo[7.4.0.0³,⁷]trideca-1(13),2,5,9,11-pentaen-5-yl}ethan-1-ol

> <ALOGPS_LOGP>
0.74

> <JCHEM_LOGP>
0.517401492333333

> <ALOGPS_LOGS>
-2.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.45779923264425

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.898777327082726

> <JCHEM_PKA_STRONGEST_BASIC>
3.903643164491303

> <JCHEM_POLAR_SURFACE_AREA>
61.61000000000001

> <JCHEM_REFRACTIVITY>
77.08249999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.41e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{6,12-dimethyl-4-thia-2,7,11,13-tetraazatricyclo[7.4.0.0³,⁷]trideca-1(13),2,5,9,11-pentaen-5-yl}ethanol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0259006
     RDKit          3D
Thiochrome
 32 34  0  0  0  0  0  0  0  0999 V2000
   -2.4132   -1.7338    0.5573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7104   -0.6191   -0.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4217    0.1325   -1.0099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8912    0.0678   -1.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4667    1.4205   -0.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2415    1.6673    0.4706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3523    1.3325   -1.7787 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.1312    0.7237   -0.9331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3442    1.1523   -1.0186 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3454    0.5051   -0.2498 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6415    0.9197   -0.3043 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6129    0.3421    0.3998 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0128    0.8075    0.3261 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2778   -0.6816    1.1826 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0300   -1.1437    1.2878 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9885   -0.5484    0.5530 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6358   -1.0847    0.6965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3336   -0.3403   -0.1456 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1463   -2.2339   -0.0956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6982   -2.5065    0.8757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9340   -1.3381    1.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1120   -0.1349   -2.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3702   -0.7110   -0.6614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0149    2.2436   -1.4552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5477    1.3795   -1.1081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2405    2.6160    0.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4651    0.9494    1.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0670    1.8209   -0.1628 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6409    0.1391   -0.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7882   -1.9787    1.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3487   -0.9956    1.7721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5645   -2.1693    0.4292 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  1  0
  5  6  1  0
  3  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18  2  1  0
 18  8  1  0
 16 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
 13 27  1  0
 13 28  1  0
 13 29  1  0
 15 30  1  0
 17 31  1  0
 17 32  1  0
M  END

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       2.983  -6.323   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.459  -4.859   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.554  -3.613   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.014  -3.613   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.244  -4.947   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.296  -4.947   0.000  0.00  0.00           O+0
HETATM    7  S   UNK     0       3.459  -2.367   0.000  0.00  0.00           S+0
HETATM    8  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       6.258  -2.073   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       7.591  -2.843   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       8.925  -2.073   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      10.259  -2.843   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.592  -2.073   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      10.259  -4.383   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       8.925  -5.153   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.591  -4.383   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.258  -5.153   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       4.924  -4.383   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   18                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7    3    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17    2    8                                                  
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

COMPND    HMDB0259006
HETATM    1  C1  UNL     1      -2.413  -1.734   0.557  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.710  -0.619  -0.221  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.422   0.132  -1.010  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.891   0.068  -1.284  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.467   1.420  -0.868  1.00  0.00           C  
HETATM    6  O1  UNL     1      -4.242   1.667   0.471  1.00  0.00           O  
HETATM    7  S1  UNL     1      -1.352   1.333  -1.779  1.00  0.00           S  
HETATM    8  C6  UNL     1       0.131   0.724  -0.933  1.00  0.00           C  
HETATM    9  N1  UNL     1       1.344   1.152  -1.019  1.00  0.00           N  
HETATM   10  C7  UNL     1       2.345   0.505  -0.250  1.00  0.00           C  
HETATM   11  N2  UNL     1       3.642   0.920  -0.304  1.00  0.00           N  
HETATM   12  C8  UNL     1       4.613   0.342   0.400  1.00  0.00           C  
HETATM   13  C9  UNL     1       6.013   0.808   0.326  1.00  0.00           C  
HETATM   14  N3  UNL     1       4.278  -0.682   1.183  1.00  0.00           N  
HETATM   15  C10 UNL     1       3.030  -1.144   1.288  1.00  0.00           C  
HETATM   16  C11 UNL     1       1.988  -0.548   0.553  1.00  0.00           C  
HETATM   17  C12 UNL     1       0.636  -1.085   0.697  1.00  0.00           C  
HETATM   18  N4  UNL     1      -0.334  -0.340  -0.146  1.00  0.00           N  
HETATM   19  H1  UNL     1      -3.146  -2.234  -0.096  1.00  0.00           H  
HETATM   20  H2  UNL     1      -1.698  -2.507   0.876  1.00  0.00           H  
HETATM   21  H3  UNL     1      -2.934  -1.338   1.426  1.00  0.00           H  
HETATM   22  H4  UNL     1      -4.112  -0.135  -2.345  1.00  0.00           H  
HETATM   23  H5  UNL     1      -4.370  -0.711  -0.661  1.00  0.00           H  
HETATM   24  H6  UNL     1      -4.015   2.244  -1.455  1.00  0.00           H  
HETATM   25  H7  UNL     1      -5.548   1.379  -1.108  1.00  0.00           H  
HETATM   26  H8  UNL     1      -4.240   2.616   0.698  1.00  0.00           H  
HETATM   27  H9  UNL     1       6.465   0.949   1.332  1.00  0.00           H  
HETATM   28  H10 UNL     1       6.067   1.821  -0.163  1.00  0.00           H  
HETATM   29  H11 UNL     1       6.641   0.139  -0.299  1.00  0.00           H  
HETATM   30  H12 UNL     1       2.788  -1.979   1.933  1.00  0.00           H  
HETATM   31  H13 UNL     1       0.349  -0.996   1.772  1.00  0.00           H  
HETATM   32  H14 UNL     1       0.565  -2.169   0.429  1.00  0.00           H  
CONECT    1    2   19   20   21
CONECT    2    3    3   18
CONECT    3    4    7
CONECT    4    5   22   23
CONECT    5    6   24   25
CONECT    6   26
CONECT    7    8
CONECT    8    9    9   18
CONECT    9   10
CONECT   10   11   11   16
CONECT   11   12
CONECT   12   13   14   14
CONECT   13   27   28   29
CONECT   14   15
CONECT   15   16   16   30
CONECT   16   17
CONECT   17   18   31   32
END

HMDB0259006
     RDKit          3D
Thiochrome
 32 34  0  0  0  0  0  0  0  0999 V2000
   -2.4132   -1.7338    0.5573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7104   -0.6191   -0.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4217    0.1325   -1.0099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8912    0.0678   -1.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4667    1.4205   -0.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2415    1.6673    0.4706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3523    1.3325   -1.7787 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.1312    0.7237   -0.9331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3442    1.1523   -1.0186 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3454    0.5051   -0.2498 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6415    0.9197   -0.3043 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6129    0.3421    0.3998 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0128    0.8075    0.3261 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2778   -0.6816    1.1826 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0300   -1.1437    1.2878 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9885   -0.5484    0.5530 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6358   -1.0847    0.6965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3336   -0.3403   -0.1456 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1463   -2.2339   -0.0956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6982   -2.5065    0.8757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9340   -1.3381    1.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1120   -0.1349   -2.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3702   -0.7110   -0.6614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0149    2.2436   -1.4552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5477    1.3795   -1.1081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2405    2.6160    0.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4651    0.9494    1.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0670    1.8209   -0.1628 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6409    0.1391   -0.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7882   -1.9787    1.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3487   -0.9956    1.7721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5645   -2.1693    0.4292 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  1  0
  5  6  1  0
  3  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18  2  1  0
 18  8  1  0
 16 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
 13 27  1  0
 13 28  1  0
 13 29  1  0
 15 30  1  0
 17 31  1  0
 17 32  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2,7-Dimethylthiochromine-8-ethanol	HMDB

Chemical Formula

C₁₂H₁₄N₄OS

Average Molecular Weight

262.33

Monoisotopic Molecular Weight

262.088832261

IUPAC Name

2-{6,12-dimethyl-4-thia-2,7,11,13-tetraazatricyclo[7.4.0.0³,⁷]trideca-1(13),2,5,9,11-pentaen-5-yl}ethan-1-ol

Traditional Name

2-{6,12-dimethyl-4-thia-2,7,11,13-tetraazatricyclo[7.4.0.0³,⁷]trideca-1(13),2,5,9,11-pentaen-5-yl}ethanol

CAS Registry Number

Not Available

SMILES

CC1=C(CCO)SC2=NC3=NC(C)=NC=C3CN12

InChI Identifier

InChI=1S/C12H14N4OS/c1-7-10(3-4-17)18-12-15-11-9(6-16(7)12)5-13-8(2)14-11/h5,17H,3-4,6H2,1-2H3

InChI Key

GTQXMAIXVFLYKF-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrimidines and pyrimidine derivatives. Pyrimidines and pyrimidine derivatives are compounds containing a pyrimidne ring, which is a six-member aromatic heterocycle which consists of two nitrogen atoms (at positions 1 and 3) and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazines

Sub Class

Pyrimidines and pyrimidine derivatives

Direct Parent

Pyrimidines and pyrimidine derivatives

Alternative Parents

Substituents

Pyrimidine
Heteroaromatic compound
Thiazole
Azole
Isothiourea
Azacycle
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
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	0.74	ALOGPS
logP	0.52	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	15.9	ChemAxon
pKa (Strongest Basic)	3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	61.61 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	77.08 m³·mol⁻¹	ChemAxon
Polarizability	28.17 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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-2H]-	191.922	30932474
DeepCCS	[M+Na]+	166.995	30932474
AllCCS	[M+H]+	158.0	32859911
AllCCS	[M+H-H2O]+	154.4	32859911
AllCCS	[M+NH4]+	161.3	32859911
AllCCS	[M+Na]+	162.2	32859911
AllCCS	[M-H]-	162.5	32859911
AllCCS	[M+Na-2H]-	162.4	32859911
AllCCS	[M+HCOO]-	162.4	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	2.62 minutes	32390414
Predicted by Siyang on May 30, 2022	9.8054 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	4.2 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	921.2 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	237.2 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	92.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	149.9 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	52.2 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	281.4 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	285.1 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	264.0 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	655.5 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	80.8 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1153.1 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	223.9 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	252.6 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	420.2 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	163.3 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	361.5 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Thiochrome	CC1=C(CCO)SC2=NC3=NC(C)=NC=C3CN12	3846.0	Standard polar	33892256
Thiochrome	CC1=C(CCO)SC2=NC3=NC(C)=NC=C3CN12	2419.8	Standard non polar	33892256
Thiochrome	CC1=C(CCO)SC2=NC3=NC(C)=NC=C3CN12	2611.2	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Thiochrome GC-MS (Non-derivatized) - 70eV, Positive	splash10-01ed-7690000000-1660c3bc63231b041812	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Thiochrome GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Thiochrome GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Thiochrome GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	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

60072

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Thiochrome

METLIN ID

Not Available

PubChem Compound

66706

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 Thiochrome (HMDB0259006)

MOL for HMDB0259006 (Thiochrome)

3D MOL for HMDB0259006 (Thiochrome)

3D SDF for HMDB0259006 (Thiochrome)

3D-SDF for HMDB0259006 (Thiochrome)

PDB for HMDB0259006 (Thiochrome)

3D PDB for HMDB0259006 (Thiochrome)

SMILES for HMDB0259006 (Thiochrome)

INCHI for HMDB0259006 (Thiochrome)

Structure for HMDB0259006 (Thiochrome)

3D Structure for HMDB0259006 (Thiochrome)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra