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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 21:56:11 UTC

Update Date

2021-09-26 23:16:54 UTC

HMDB ID

HMDB0259384

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide

Description

N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide belongs to the class of organic compounds known as chlorobenzenes. Chlorobenzenes are compounds containing one or more chlorine atoms attached to a benzene moiety. Based on a literature review very few articles have been published on N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide. This compound has been identified in human blood as reported by (PMID: 31557052 ). N-[4-cloro-3-(t-butyloxome)phenyl-2-methyl-3-furan-carbothiamide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide 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

HMDB0260023
     RDKit          3D
N-[4-Chloro-3-[(Z)-(2-methylpropan-2-yl)oxyiminomethyl]phenyl]-2-methylfuran-...
 42 43  0  0  0  0  0  0  0  0999 V2000
    4.6035    2.3146   -0.5790 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4755    1.3829    0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6121    1.7339    0.7085 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1813    0.7029    1.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3768   -0.4222    1.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3062    0.0528    0.3751 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1653   -0.7701   -0.0742 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5235   -2.1002   -0.9472 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.8496   -0.4205    0.2045 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6704   -1.0966   -0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5902   -2.4423   -0.4246 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3629   -3.0049   -0.7849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7891   -2.2690   -0.8699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3227   -3.0153   -1.3295 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.7355   -0.9207   -0.5890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9177   -0.0811   -0.6588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0516   -0.5771   -0.9865 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1980    0.1381   -1.0741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0328    0.4991   -0.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2041    1.2996   -0.5930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5623   -0.7088    0.6956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3427    1.4575    0.9652 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4661   -0.3695   -0.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2663    3.1002    0.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7265    0.4869    0.7604 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4577   -3.0965   -0.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3110   -4.0614   -1.0069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8381    0.9601   -0.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7211    1.7800    0.2510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8829    0.6239   -1.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7432    2.0624   -1.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3786   -1.5984    0.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6288   -0.5522    0.9252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0503   -0.8668    1.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1396    2.0280    1.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7275    2.1844    0.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7087    0.9029    1.6880 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5483    0.6983   -0.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
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  9 10  1  0
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  6  2  2  0
 23 10  1  0
  1 24  1  0
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  4 27  1  0
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 20 35  1  0
 21 36  1  0
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 21 38  1  0
 22 39  1  0
 22 40  1  0
 22 41  1  0
 23 42  1  0
M  END


  Mrv1652309112123562D          

 23 24  0  0  0  0            999 V2000
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0164   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7615   -2.9599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8810   -2.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4941   -3.2570    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.0525   -1.8980    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8372   -1.6431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0087   -0.8361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7933   -0.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4064   -1.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2349   -1.9402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4502   -2.1951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1910   -0.8783    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.9648    0.2258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7494    0.4807    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9210    1.2877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3079    1.8398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6948    2.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8599    2.4528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7558    1.2267    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
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 20 23  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0259384

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=C(C=CO1)C(=S)NC1=CC(C=NOC(C)(C)C)=C(Cl)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H19ClN2O2S/c1-11-14(7-8-21-11)16(23)20-13-5-6-15(18)12(9-13)10-19-22-17(2,3)4/h5-10H,1-4H3,(H,20,23)

> <INCHI_KEY>
PLGIIOKXCKDKEU-UHFFFAOYSA-N

> <FORMULA>
C17H19ClN2O2S

> <MOLECULAR_WEIGHT>
350.86

> <EXACT_MASS>
350.0855767

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
36.84649424176265

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-(3-{[(tert-butoxy)imino]methyl}-4-chlorophenyl)-2-methylfuran-3-carbothioamide

> <ALOGPS_LOGP>
5.11

> <JCHEM_LOGP>
5.052754226666666

> <ALOGPS_LOGS>
-4.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.865608596219442

> <JCHEM_PKA_STRONGEST_BASIC>
2.5216132271041984

> <JCHEM_POLAR_SURFACE_AREA>
46.760000000000005

> <JCHEM_REFRACTIVITY>
100.74390000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.43e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-{3-[(tert-butoxyimino)methyl]-4-chlorophenyl}-2-methylfuran-3-carbothioamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0260023
     RDKit          3D
N-[4-Chloro-3-[(Z)-(2-methylpropan-2-yl)oxyiminomethyl]phenyl]-2-methylfuran-...
 42 43  0  0  0  0  0  0  0  0999 V2000
    4.6035    2.3146   -0.5790 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4755    1.3829    0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6121    1.7339    0.7085 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1813    0.7029    1.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3768   -0.4222    1.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3062    0.0528    0.3751 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1653   -0.7701   -0.0742 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5235   -2.1002   -0.9472 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.8496   -0.4205    0.2045 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6704   -1.0966   -0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5902   -2.4423   -0.4246 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3629   -3.0049   -0.7849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7891   -2.2690   -0.8699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3227   -3.0153   -1.3295 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.7355   -0.9207   -0.5890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9177   -0.0811   -0.6588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0516   -0.5771   -0.9865 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1980    0.1381   -1.0741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0328    0.4991   -0.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2041    1.2996   -0.5930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5623   -0.7088    0.6956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3427    1.4575    0.9652 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4661   -0.3695   -0.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7033    1.8650   -0.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1302    2.8517   -1.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2663    3.1002    0.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1109    0.6722    1.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5378   -1.4242    1.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    0.4869    0.7604 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4577   -3.0965   -0.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3110   -4.0614   -1.0069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8381    0.9601   -0.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7211    1.7800    0.2510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8829    0.6239   -1.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7432    2.0624   -1.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3786   -1.5984    0.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6288   -0.5522    0.9252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0503   -0.8668    1.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1396    2.0280    1.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7275    2.1844    0.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7087    0.9029    1.6880 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5483    0.6983   -0.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  2  3
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 19 22  1  0
 15 23  2  0
  6  2  2  0
 23 10  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
  9 29  1  0
 11 30  1  0
 12 31  1  0
 16 32  1  0
 20 33  1  0
 20 34  1  0
 20 35  1  0
 21 36  1  0
 21 37  1  0
 21 38  1  0
 22 39  1  0
 22 40  1  0
 22 41  1  0
 23 42  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.913  -5.525   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.437  -6.990   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.897  -6.990   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.421  -5.525   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.378  -5.049   0.000  0.00  0.00           C+0
HETATM    8  S   UNK     0       6.522  -6.080   0.000  0.00  0.00           S+0
HETATM    9  N   UNK     0       5.698  -3.543   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       7.163  -3.067   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.483  -1.561   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.947  -1.085   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.092  -2.115   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.772  -3.622   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.307  -4.098   0.000  0.00  0.00           C+0
HETATM   16 Cl   UNK     0      11.557  -1.639   0.000  0.00  0.00          Cl+0
HETATM   17  C   UNK     0       9.268   0.422   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      10.732   0.897   0.000  0.00  0.00           N+0
HETATM   19  O   UNK     0      11.052   2.404   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.908   3.434   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.764   4.465   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.939   4.579   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.878   2.290   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    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16   13                                                            
CONECT   17   12   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

COMPND    HMDB0260023
HETATM    1  C1  UNL     1       4.603   2.315  -0.579  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.476   1.383   0.146  1.00  0.00           C  
HETATM    3  O1  UNL     1       6.612   1.734   0.709  1.00  0.00           O  
HETATM    4  C3  UNL     1       7.181   0.703   1.285  1.00  0.00           C  
HETATM    5  C4  UNL     1       6.377  -0.422   1.102  1.00  0.00           C  
HETATM    6  C5  UNL     1       5.306   0.053   0.375  1.00  0.00           C  
HETATM    7  C6  UNL     1       4.165  -0.770  -0.074  1.00  0.00           C  
HETATM    8  S1  UNL     1       4.523  -2.100  -0.947  1.00  0.00           S  
HETATM    9  N1  UNL     1       2.850  -0.420   0.204  1.00  0.00           N  
HETATM   10  C7  UNL     1       1.670  -1.097  -0.140  1.00  0.00           C  
HETATM   11  C8  UNL     1       1.590  -2.442  -0.425  1.00  0.00           C  
HETATM   12  C9  UNL     1       0.363  -3.005  -0.785  1.00  0.00           C  
HETATM   13  C10 UNL     1      -0.789  -2.269  -0.870  1.00  0.00           C  
HETATM   14 CL1  UNL     1      -2.323  -3.015  -1.329  1.00  0.00          CL  
HETATM   15  C11 UNL     1      -0.736  -0.921  -0.589  1.00  0.00           C  
HETATM   16  C12 UNL     1      -1.918  -0.081  -0.659  1.00  0.00           C  
HETATM   17  N2  UNL     1      -3.052  -0.577  -0.987  1.00  0.00           N  
HETATM   18  O2  UNL     1      -4.198   0.138  -1.074  1.00  0.00           O  
HETATM   19  C13 UNL     1      -5.033   0.499  -0.012  1.00  0.00           C  
HETATM   20  C14 UNL     1      -6.204   1.300  -0.593  1.00  0.00           C  
HETATM   21  C15 UNL     1      -5.562  -0.709   0.696  1.00  0.00           C  
HETATM   22  C16 UNL     1      -4.343   1.458   0.965  1.00  0.00           C  
HETATM   23  C17 UNL     1       0.466  -0.370  -0.237  1.00  0.00           C  
HETATM   24  H1  UNL     1       3.703   1.865  -0.992  1.00  0.00           H  
HETATM   25  H2  UNL     1       5.130   2.852  -1.394  1.00  0.00           H  
HETATM   26  H3  UNL     1       4.266   3.100   0.158  1.00  0.00           H  
HETATM   27  H4  UNL     1       8.111   0.672   1.823  1.00  0.00           H  
HETATM   28  H5  UNL     1       6.538  -1.424   1.439  1.00  0.00           H  
HETATM   29  H6  UNL     1       2.726   0.487   0.760  1.00  0.00           H  
HETATM   30  H7  UNL     1       2.458  -3.097  -0.361  1.00  0.00           H  
HETATM   31  H8  UNL     1       0.311  -4.061  -1.007  1.00  0.00           H  
HETATM   32  H9  UNL     1      -1.838   0.960  -0.434  1.00  0.00           H  
HETATM   33  H10 UNL     1      -6.721   1.780   0.251  1.00  0.00           H  
HETATM   34  H11 UNL     1      -6.883   0.624  -1.187  1.00  0.00           H  
HETATM   35  H12 UNL     1      -5.743   2.062  -1.260  1.00  0.00           H  
HETATM   36  H13 UNL     1      -5.379  -1.598   0.073  1.00  0.00           H  
HETATM   37  H14 UNL     1      -6.629  -0.552   0.925  1.00  0.00           H  
HETATM   38  H15 UNL     1      -5.050  -0.867   1.671  1.00  0.00           H  
HETATM   39  H16 UNL     1      -5.140   2.028   1.526  1.00  0.00           H  
HETATM   40  H17 UNL     1      -3.728   2.184   0.397  1.00  0.00           H  
HETATM   41  H18 UNL     1      -3.709   0.903   1.688  1.00  0.00           H  
HETATM   42  H19 UNL     1       0.548   0.698  -0.007  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3    6    6
CONECT    3    4
CONECT    4    5    5   27
CONECT    5    6   28
CONECT    6    7
CONECT    7    8    8    9
CONECT    9   10   29
CONECT   10   11   11   23
CONECT   11   12   30
CONECT   12   13   13   31
CONECT   13   14   15
CONECT   15   16   23   23
CONECT   16   17   17   32
CONECT   17   18
CONECT   18   19
CONECT   19   20   21   22
CONECT   20   33   34   35
CONECT   21   36   37   38
CONECT   22   39   40   41
CONECT   23   42
END

HMDB0260023
     RDKit          3D
N-[4-Chloro-3-[(Z)-(2-methylpropan-2-yl)oxyiminomethyl]phenyl]-2-methylfuran-...
 42 43  0  0  0  0  0  0  0  0999 V2000
    4.6035    2.3146   -0.5790 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4755    1.3829    0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6121    1.7339    0.7085 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1813    0.7029    1.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3768   -0.4222    1.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3062    0.0528    0.3751 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1653   -0.7701   -0.0742 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5235   -2.1002   -0.9472 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.8496   -0.4205    0.2045 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6704   -1.0966   -0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5902   -2.4423   -0.4246 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3629   -3.0049   -0.7849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7891   -2.2690   -0.8699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3227   -3.0153   -1.3295 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.7355   -0.9207   -0.5890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9177   -0.0811   -0.6588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0516   -0.5771   -0.9865 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1980    0.1381   -1.0741 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0328    0.4991   -0.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2041    1.2996   -0.5930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5623   -0.7088    0.6956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3427    1.4575    0.9652 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4661   -0.3695   -0.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7033    1.8650   -0.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1302    2.8517   -1.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2663    3.1002    0.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1109    0.6722    1.8229 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5378   -1.4242    1.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    0.4869    0.7604 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4577   -3.0965   -0.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3110   -4.0614   -1.0069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8381    0.9601   -0.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7211    1.7800    0.2510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8829    0.6239   -1.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7432    2.0624   -1.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3786   -1.5984    0.0733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6288   -0.5522    0.9252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0503   -0.8668    1.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1396    2.0280    1.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7275    2.1844    0.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7087    0.9029    1.6880 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5483    0.6983   -0.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  2  3
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 19 22  1  0
 15 23  2  0
  6  2  2  0
 23 10  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
  9 29  1  0
 11 30  1  0
 12 31  1  0
 16 32  1  0
 20 33  1  0
 20 34  1  0
 20 35  1  0
 21 36  1  0
 21 37  1  0
 21 38  1  0
 22 39  1  0
 22 40  1  0
 22 41  1  0
 23 42  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₇H₁₉ClN₂O₂S

Average Molecular Weight

350.86

Monoisotopic Molecular Weight

350.0855767

IUPAC Name

N-(3-{[(tert-butoxy)imino]methyl}-4-chlorophenyl)-2-methylfuran-3-carbothioamide

Traditional Name

N-{3-[(tert-butoxyimino)methyl]-4-chlorophenyl}-2-methylfuran-3-carbothioamide

CAS Registry Number

Not Available

SMILES

CC1=C(C=CO1)C(=S)NC1=CC(C=NOC(C)(C)C)=C(Cl)C=C1

InChI Identifier

InChI=1S/C17H19ClN2O2S/c1-11-14(7-8-21-11)16(23)20-13-5-6-15(18)12(9-13)10-19-22-17(2,3)4/h5-10H,1-4H3,(H,20,23)

InChI Key

PLGIIOKXCKDKEU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as chlorobenzenes. Chlorobenzenes are compounds containing one or more chlorine atoms attached to a benzene moiety.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Halobenzenes

Direct Parent

Chlorobenzenes

Alternative Parents

Substituents

Chlorobenzene
Aryl chloride
Aryl halide
Furan
Thioamide
Heteroaromatic compound
Organoheterocyclic compound
Thiocarboxylic acid amide
Oxacycle
Thiocarbonyl group
Organic nitrogen compound
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Organopnictogen compound
Organic oxygen compound
Hydrocarbon derivative
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	5.11	ALOGPS
logP	5.05	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	10.87	ChemAxon
pKa (Strongest Basic)	2.52	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.76 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	100.74 m³·mol⁻¹	ChemAxon
Polarizability	36.85 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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]+	187.149	30932474
DeepCCS	[M-H]-	184.791	30932474
DeepCCS	[M-2H]-	218.728	30932474
DeepCCS	[M+Na]+	194.036	30932474

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.	5.92 minutes	32390414
Predicted by Siyang on May 30, 2022	22.2223 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.01 minutes	32390414

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide,1TMS,isomer #1	CC1=C(C(=S)N(C2=CC=C(Cl)C(C=NOC(C)(C)C)=C2)[Si](C)(C)C)C=CO1	2617.6	Semi standard non polar	33892256
N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide,1TMS,isomer #1	CC1=C(C(=S)N(C2=CC=C(Cl)C(C=NOC(C)(C)C)=C2)[Si](C)(C)C)C=CO1	2522.5	Standard non polar	33892256
N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide,1TMS,isomer #1	CC1=C(C(=S)N(C2=CC=C(Cl)C(C=NOC(C)(C)C)=C2)[Si](C)(C)C)C=CO1	3389.1	Standard polar	33892256
N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide,1TBDMS,isomer #1	CC1=C(C(=S)N(C2=CC=C(Cl)C(C=NOC(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=CO1	2824.3	Semi standard non polar	33892256
N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide,1TBDMS,isomer #1	CC1=C(C(=S)N(C2=CC=C(Cl)C(C=NOC(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=CO1	2722.8	Standard non polar	33892256
N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide,1TBDMS,isomer #1	CC1=C(C(=S)N(C2=CC=C(Cl)C(C=NOC(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=CO1	3414.4	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-9232000000-8e3ea435368d4a41633b	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	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

2272476

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

371138

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 N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide (HMDB0259384)

MOL for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

3D MOL for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

3D SDF for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

3D-SDF for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

PDB for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

3D PDB for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

SMILES for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

INCHI for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

Structure for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

3D Structure for HMDB0259384 (N-[4-Cloro-3-(T-butyloxome)phenyl-2-methyl-3-furan-carbothiamide)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra