Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 07:02:19 UTC

Update Date

2021-09-26 23:01:16 UTC

HMDB ID

HMDB0250065

Secondary Accession Numbers

None

Metabolite Identification

Common Name

4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole

Description

4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole, also known as MMIMT, belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. Based on a literature review very few articles have been published on 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4-(2-methoxyphenyl)-2-((5-methyl-1h-imidazol-4-yl)methyl)thiazole is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole 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

HMDB0250065
     RDKit          3D
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole
 35 37  0  0  0  0  0  0  0  0999 V2000
   -2.8554    1.7090    1.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1895    0.8311    0.4649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8273   -0.3361    0.0770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0983   -0.6378    0.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7185   -1.8027    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0264   -2.6444   -0.7204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7431   -2.3484   -1.1844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1426   -1.1860   -0.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7769   -0.8418   -1.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0843   -1.6853   -2.0888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3852   -0.8240   -2.3036 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316    0.5267   -1.3357 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9271    1.6912   -1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7947    1.5044    0.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5916    2.0694    1.2861 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5545    1.6974    2.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3714    0.8790    1.4625 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9288    0.7442    0.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5767   -0.0716   -0.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1787    0.2590   -0.8989 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1869    1.0922    2.2132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1954    2.5048    1.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7574    2.0981    0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5997    0.0466    1.1953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7023   -2.0199    0.4980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5293   -3.5523   -1.0194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2527   -3.0432   -1.8506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3955   -2.6594   -2.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5624    1.8004   -2.0154 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3460    2.6337   -1.0385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6511    1.9934    3.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2175    0.4352    1.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6773    0.1657   -0.8066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1816    0.1287   -1.8560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4628   -1.1570   -0.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 12 20  2  0
  8  3  1  0
 20  9  1  0
 18 14  2  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
 10 28  1  0
 13 29  1  0
 13 30  1  0
 16 31  1  0
 17 32  1  0
 19 33  1  0
 19 34  1  0
 19 35  1  0
M  END

  Mrv1652309112109022D          

 20 22  0  0  0  0            999 V2000
    0.4380   -3.0425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4380   -3.8675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1055   -4.3524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8505   -5.1370    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0255   -5.1370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2294   -4.3524    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8901   -4.0975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5032   -4.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3102   -4.4780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7227   -5.1924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1706   -5.8055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4170   -5.4700    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.5432   -5.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0281   -4.6112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8486   -4.6975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1841   -5.4512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6992   -6.1186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8787   -6.0324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3938   -6.6998    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5733   -6.6136    0.0000 C   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  2  0  0  0  0
  5  6  1  0  0  0  0
  2  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
  8 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0250065

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC=CC=C1C1=CSC(CC2=C(C)NC=N2)=N1

> <INCHI_IDENTIFIER>
InChI=1S/C15H15N3OS/c1-10-12(17-9-16-10)7-15-18-13(8-20-15)11-5-3-4-6-14(11)19-2/h3-6,8-9H,7H2,1-2H3,(H,16,17)

> <INCHI_KEY>
NADMOKMSPBJASV-UHFFFAOYSA-N

> <FORMULA>
C15H15N3OS

> <MOLECULAR_WEIGHT>
285.37

> <EXACT_MASS>
285.093583289

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
30.16713059758036

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(2-methoxyphenyl)-2-[(5-methyl-1H-imidazol-4-yl)methyl]-1,3-thiazole

> <ALOGPS_LOGP>
3.52

> <JCHEM_LOGP>
2.9317891943333327

> <ALOGPS_LOGS>
-4.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.96154080360673

> <JCHEM_PKA_STRONGEST_BASIC>
7.040258157285991

> <JCHEM_POLAR_SURFACE_AREA>
50.8

> <JCHEM_REFRACTIVITY>
79.3889

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.06e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-(2-methoxyphenyl)-2-[(5-methyl-1H-imidazol-4-yl)methyl]-1,3-thiazole

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0250065
     RDKit          3D
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole
 35 37  0  0  0  0  0  0  0  0999 V2000
   -2.8554    1.7090    1.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1895    0.8311    0.4649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8273   -0.3361    0.0770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0983   -0.6378    0.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7185   -1.8027    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0264   -2.6444   -0.7204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7431   -2.3484   -1.1844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1426   -1.1860   -0.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7769   -0.8418   -1.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0843   -1.6853   -2.0888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3852   -0.8240   -2.3036 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316    0.5267   -1.3357 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9271    1.6912   -1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7947    1.5044    0.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5916    2.0694    1.2861 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5545    1.6974    2.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3714    0.8790    1.4625 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9288    0.7442    0.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5767   -0.0716   -0.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1787    0.2590   -0.8989 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1869    1.0922    2.2132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1954    2.5048    1.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7574    2.0981    0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5997    0.0466    1.1953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7023   -2.0199    0.4980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5293   -3.5523   -1.0194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2527   -3.0432   -1.8506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3955   -2.6594   -2.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5624    1.8004   -2.0154 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3460    2.6337   -1.0385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6511    1.9934    3.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2175    0.4352    1.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6773    0.1657   -0.8066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1816    0.1287   -1.8560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4628   -1.1570   -0.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 12 20  2  0
  8  3  1  0
 20  9  1  0
 18 14  2  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
 10 28  1  0
 13 29  1  0
 13 30  1  0
 16 31  1  0
 17 32  1  0
 19 33  1  0
 19 34  1  0
 19 35  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       0.818  -5.679   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.818  -7.219   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.064  -8.124   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       1.588  -9.589   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       0.048  -9.589   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -0.428  -8.124   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       3.528  -7.649   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.673  -8.679   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       6.179  -8.359   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       6.949  -9.693   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.919 -10.837   0.000  0.00  0.00           C+0
HETATM   12  S   UNK     0       4.512 -10.211   0.000  0.00  0.00           S+0
HETATM   13  C   UNK     0       8.481  -9.854   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.386  -8.608   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.917  -8.769   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.544 -10.175   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.638 -11.421   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.107 -11.260   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.202 -12.506   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.670 -12.345   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    2                                                       
CONECT    7    3    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11    8                                                       
CONECT   13   10   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

COMPND    HMDB0250065
HETATM    1  C1  UNL     1      -2.855   1.709   1.332  1.00  0.00           C  
HETATM    2  O1  UNL     1      -2.190   0.831   0.465  1.00  0.00           O  
HETATM    3  C2  UNL     1      -2.827  -0.336   0.077  1.00  0.00           C  
HETATM    4  C3  UNL     1      -4.098  -0.638   0.531  1.00  0.00           C  
HETATM    5  C4  UNL     1      -4.718  -1.803   0.137  1.00  0.00           C  
HETATM    6  C5  UNL     1      -4.026  -2.644  -0.720  1.00  0.00           C  
HETATM    7  C6  UNL     1      -2.743  -2.348  -1.184  1.00  0.00           C  
HETATM    8  C7  UNL     1      -2.143  -1.186  -0.781  1.00  0.00           C  
HETATM    9  C8  UNL     1      -0.777  -0.842  -1.253  1.00  0.00           C  
HETATM   10  C9  UNL     1      -0.084  -1.685  -2.089  1.00  0.00           C  
HETATM   11  S1  UNL     1       1.385  -0.824  -2.304  1.00  0.00           S  
HETATM   12  C10 UNL     1       1.032   0.527  -1.336  1.00  0.00           C  
HETATM   13  C11 UNL     1       1.927   1.691  -1.089  1.00  0.00           C  
HETATM   14  C12 UNL     1       2.795   1.504   0.091  1.00  0.00           C  
HETATM   15  N1  UNL     1       2.592   2.069   1.286  1.00  0.00           N  
HETATM   16  C13 UNL     1       3.554   1.697   2.152  1.00  0.00           C  
HETATM   17  N2  UNL     1       4.371   0.879   1.462  1.00  0.00           N  
HETATM   18  C14 UNL     1       3.929   0.744   0.197  1.00  0.00           C  
HETATM   19  C15 UNL     1       4.577  -0.072  -0.839  1.00  0.00           C  
HETATM   20  N3  UNL     1      -0.179   0.259  -0.899  1.00  0.00           N  
HETATM   21  H1  UNL     1      -3.187   1.092   2.213  1.00  0.00           H  
HETATM   22  H2  UNL     1      -2.195   2.505   1.734  1.00  0.00           H  
HETATM   23  H3  UNL     1      -3.757   2.098   0.848  1.00  0.00           H  
HETATM   24  H4  UNL     1      -4.600   0.047   1.195  1.00  0.00           H  
HETATM   25  H5  UNL     1      -5.702  -2.020   0.498  1.00  0.00           H  
HETATM   26  H6  UNL     1      -4.529  -3.552  -1.019  1.00  0.00           H  
HETATM   27  H7  UNL     1      -2.253  -3.043  -1.851  1.00  0.00           H  
HETATM   28  H8  UNL     1      -0.396  -2.659  -2.509  1.00  0.00           H  
HETATM   29  H9  UNL     1       2.562   1.800  -2.015  1.00  0.00           H  
HETATM   30  H10 UNL     1       1.346   2.634  -1.039  1.00  0.00           H  
HETATM   31  H11 UNL     1       3.651   1.993   3.185  1.00  0.00           H  
HETATM   32  H12 UNL     1       5.217   0.435   1.891  1.00  0.00           H  
HETATM   33  H13 UNL     1       5.677   0.166  -0.807  1.00  0.00           H  
HETATM   34  H14 UNL     1       4.182   0.129  -1.856  1.00  0.00           H  
HETATM   35  H15 UNL     1       4.463  -1.157  -0.646  1.00  0.00           H  
CONECT    1    2   21   22   23
CONECT    2    3
CONECT    3    4    4    8
CONECT    4    5   24
CONECT    5    6    6   25
CONECT    6    7   26
CONECT    7    8    8   27
CONECT    8    9
CONECT    9   10   10   20
CONECT   10   11   28
CONECT   11   12
CONECT   12   13   20   20
CONECT   13   14   29   30
CONECT   14   15   18   18
CONECT   15   16   16
CONECT   16   17   31
CONECT   17   18   32
CONECT   18   19
CONECT   19   33   34   35
END

HMDB0250065
     RDKit          3D
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole
 35 37  0  0  0  0  0  0  0  0999 V2000
   -2.8554    1.7090    1.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1895    0.8311    0.4649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8273   -0.3361    0.0770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0983   -0.6378    0.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7185   -1.8027    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0264   -2.6444   -0.7204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7431   -2.3484   -1.1844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1426   -1.1860   -0.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7769   -0.8418   -1.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0843   -1.6853   -2.0888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3852   -0.8240   -2.3036 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316    0.5267   -1.3357 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9271    1.6912   -1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7947    1.5044    0.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5916    2.0694    1.2861 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5545    1.6974    2.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3714    0.8790    1.4625 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9288    0.7442    0.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5767   -0.0716   -0.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1787    0.2590   -0.8989 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1869    1.0922    2.2132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1954    2.5048    1.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7574    2.0981    0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5997    0.0466    1.1953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7023   -2.0199    0.4980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5293   -3.5523   -1.0194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2527   -3.0432   -1.8506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3955   -2.6594   -2.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5624    1.8004   -2.0154 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3460    2.6337   -1.0385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6511    1.9934    3.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2175    0.4352    1.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6773    0.1657   -0.8066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1816    0.1287   -1.8560 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4628   -1.1570   -0.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 12 20  2  0
  8  3  1  0
 20  9  1  0
 18 14  2  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
 10 28  1  0
 13 29  1  0
 13 30  1  0
 16 31  1  0
 17 32  1  0
 19 33  1  0
 19 34  1  0
 19 35  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
4-(2-Methoxyphenyl)-2-(4(5)-methyl-5(4)-imidazolylmethyl)thiazole	HMDB
MMIMT	HMDB

Chemical Formula

C₁₅H₁₅N₃OS

Average Molecular Weight

285.37

Monoisotopic Molecular Weight

285.093583289

IUPAC Name

4-(2-methoxyphenyl)-2-[(5-methyl-1H-imidazol-4-yl)methyl]-1,3-thiazole

Traditional Name

4-(2-methoxyphenyl)-2-[(5-methyl-1H-imidazol-4-yl)methyl]-1,3-thiazole

CAS Registry Number

Not Available

SMILES

COC1=CC=CC=C1C1=CSC(CC2=C(C)NC=N2)=N1

InChI Identifier

InChI=1S/C15H15N3OS/c1-10-12(17-9-16-10)7-15-18-13(8-20-15)11-5-3-4-6-14(11)19-2/h3-6,8-9H,7H2,1-2H3,(H,16,17)

InChI Key

NADMOKMSPBJASV-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenoxy compound
Anisole
Methoxybenzene
2,4-disubstituted 1,3-thiazole
Alkyl aryl ether
Monocyclic benzene moiety
Heteroaromatic compound
Azole
Thiazole
Imidazole
Azacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	3.52	ALOGPS
logP	2.93	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	13.96	ChemAxon
pKa (Strongest Basic)	7.04	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	50.8 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	79.39 m³·mol⁻¹	ChemAxon
Polarizability	30.17 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+H]+	167.035	30932474
DeepCCS	[M-H]-	164.677	30932474
DeepCCS	[M-2H]-	197.563	30932474
DeepCCS	[M+Na]+	173.128	30932474
AllCCS	[M+H]+	166.0	32859911
AllCCS	[M+H-H2O]+	162.4	32859911
AllCCS	[M+NH4]+	169.3	32859911
AllCCS	[M+Na]+	170.3	32859911
AllCCS	[M-H]-	168.6	32859911
AllCCS	[M+Na-2H]-	168.2	32859911
AllCCS	[M+HCOO]-	167.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole	COC1=CC=CC=C1C1=CSC(CC2=C(C)NC=N2)=N1	3332.5	Standard polar	33892256
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole	COC1=CC=CC=C1C1=CSC(CC2=C(C)NC=N2)=N1	2412.1	Standard non polar	33892256
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole	COC1=CC=CC=C1C1=CSC(CC2=C(C)NC=N2)=N1	2694.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole,1TMS,isomer #1	COC1=CC=CC=C1C1=CSC(CC2=C(C)N([Si](C)(C)C)C=N2)=N1	2741.0	Semi standard non polar	33892256
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole,1TMS,isomer #1	COC1=CC=CC=C1C1=CSC(CC2=C(C)N([Si](C)(C)C)C=N2)=N1	2729.3	Standard non polar	33892256
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole,1TMS,isomer #1	COC1=CC=CC=C1C1=CSC(CC2=C(C)N([Si](C)(C)C)C=N2)=N1	3362.1	Standard polar	33892256
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole,1TBDMS,isomer #1	COC1=CC=CC=C1C1=CSC(CC2=C(C)N([Si](C)(C)C(C)(C)C)C=N2)=N1	2964.3	Semi standard non polar	33892256
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole,1TBDMS,isomer #1	COC1=CC=CC=C1C1=CSC(CC2=C(C)N([Si](C)(C)C(C)(C)C)C=N2)=N1	2921.1	Standard non polar	33892256
4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole,1TBDMS,isomer #1	COC1=CC=CC=C1C1=CSC(CC2=C(C)N([Si](C)(C)C(C)(C)C)C=N2)=N1	3419.6	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole GC-MS (Non-derivatized) - 70eV, Positive	splash10-00du-3590000000-38932242f46c861bdc39	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole 10V, Positive-QTOF	splash10-000i-0090000000-cd6c1ed5a8c1fb61ccce	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole 20V, Positive-QTOF	splash10-000i-0090000000-fe266ae2c63f8ebf9b3e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole 40V, Positive-QTOF	splash10-0f6x-1390000000-2de5cd33b3b385e5e34b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole 10V, Negative-QTOF	splash10-001i-0190000000-f4e04e78aca5db3e6f5a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole 20V, Negative-QTOF	splash10-0f89-0390000000-7f075f310e8cfde0bedb	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole 40V, Negative-QTOF	splash10-001i-5980000000-fa05e674d6a67aab53b1	2021-10-12	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

2299775

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3035572

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 4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole (HMDB0250065)

MOL for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

3D MOL for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

3D SDF for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

3D-SDF for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

PDB for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

3D PDB for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

SMILES for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

INCHI for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

Structure for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

3D Structure for HMDB0250065 (4-(2-Methoxyphenyl)-2-((5-methyl-1H-imidazol-4-yl)methyl)thiazole)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra