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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 14:52:55 UTC

Update Date

2021-09-26 23:09:56 UTC

HMDB ID

HMDB0255278

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N'-Benzoyl-N,N'-dimethylbenzohydrazide

Description

N'-Benzoyl-N,N'-dimethylbenzohydrazide, also known as fenoperidine or hydrochloride, phenoperidine, belongs to the class of organic compounds known as benzoic acids and derivatives. These are organic compounds containing a carboxylic acid substituent attached to a benzene ring. Based on a literature review very few articles have been published on N'-Benzoyl-N,N'-dimethylbenzohydrazide. This compound has been identified in human blood as reported by (PMID: 31557052 ). N'-benzoyl-n,n'-dimethylbenzohydrazide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically N'-Benzoyl-N,N'-dimethylbenzohydrazide 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

HMDB0255278
     RDKit          3D
N'-Benzoyl-N,N'-dimethylbenzohydrazide
 36 37  0  0  0  0  0  0  0  0999 V2000
    1.0210   -2.0260   -1.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6211   -0.9761   -0.2769 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4434   -0.0950    0.3865 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8008    0.7685    1.1363 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8653    0.0638    0.4184 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7266   -0.7397   -0.2870 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1152   -0.5376   -0.2208 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6235    0.4631    0.5482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7966    1.2875    1.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4505    1.0784    1.1932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8274   -0.8588   -0.0772 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4225   -1.9589    0.5813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4061    0.3032   -0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6053    1.1645   -1.1374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7865    0.7514   -0.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8208    0.0390    0.0183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1376    0.4823    0.0302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4182    1.6983   -0.5429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4083    2.4421   -1.1082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126    1.9872   -1.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5980   -2.8381   -0.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0581   -2.5317   -1.5484 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5220   -1.6853   -2.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3982   -1.5451   -0.9095 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7935   -1.1796   -0.7840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6812    0.6475    0.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2199    2.0857    1.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7727    1.7146    1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1378   -2.5498   -0.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6140   -2.7534    0.7825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8399   -1.7668    1.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6471   -0.9361    0.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9070   -0.1282    0.4836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4303    2.0904   -0.5600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6505    3.4163   -1.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3357    2.6224   -1.5772 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  2 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 10  5  1  0
 20 15  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 12 30  1  0
 12 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 20 36  1  0
M  END


  Mrv1652309112116532D          

 20 21  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 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 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
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0255278

> <DATABASE_NAME>
hmdb

> <SMILES>
CN(N(C)C(=O)C1=CC=CC=C1)C(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H16N2O2/c1-17(15(19)13-9-5-3-6-10-13)18(2)16(20)14-11-7-4-8-12-14/h3-12H,1-2H3

> <INCHI_KEY>
PQEZHJRKUSZEBK-UHFFFAOYSA-N

> <FORMULA>
C16H16N2O2

> <MOLECULAR_WEIGHT>
268.316

> <EXACT_MASS>
268.121177763

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
27.172967570752967

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N'-benzoyl-N,N'-dimethylbenzohydrazide

> <ALOGPS_LOGP>
1.68

> <JCHEM_LOGP>
2.535963311333333

> <ALOGPS_LOGS>
-3.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.02619374938055

> <JCHEM_POLAR_SURFACE_AREA>
40.620000000000005

> <JCHEM_REFRACTIVITY>
78.46620000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.65e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N'-benzoyl-N,N'-dimethylbenzohydrazide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0255278
     RDKit          3D
N'-Benzoyl-N,N'-dimethylbenzohydrazide
 36 37  0  0  0  0  0  0  0  0999 V2000
    1.0210   -2.0260   -1.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6211   -0.9761   -0.2769 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4434   -0.0950    0.3865 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8008    0.7685    1.1363 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8653    0.0638    0.4184 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7266   -0.7397   -0.2870 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1152   -0.5376   -0.2208 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6235    0.4631    0.5482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7966    1.2875    1.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4505    1.0784    1.1932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8274   -0.8588   -0.0772 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4225   -1.9589    0.5813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4061    0.3032   -0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6053    1.1645   -1.1374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7865    0.7514   -0.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8208    0.0390    0.0183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1376    0.4823    0.0302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4182    1.6983   -0.5429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4083    2.4421   -1.1082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126    1.9872   -1.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5980   -2.8381   -0.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0581   -2.5317   -1.5484 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5220   -1.6853   -2.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3982   -1.5451   -0.9095 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7935   -1.1796   -0.7840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6812    0.6475    0.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2199    2.0857    1.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7727    1.7146    1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1378   -2.5498   -0.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6140   -2.7534    0.7825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8399   -1.7668    1.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6471   -0.9361    0.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9070   -0.1282    0.4836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4303    2.0904   -0.5600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6505    3.4163   -1.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3357    2.6224   -1.5772 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  2 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 10  5  1  0
 20 15  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 12 30  1  0
 12 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 20 36  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  N   UNK     0       2.667  -4.620   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       4.001  -5.390   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5                                                       
CONECT   11    2   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   42    0
END

COMPND    HMDB0255278
HETATM    1  C1  UNL     1       1.021  -2.026  -1.165  1.00  0.00           C  
HETATM    2  N1  UNL     1       0.621  -0.976  -0.277  1.00  0.00           N  
HETATM    3  C2  UNL     1       1.443  -0.095   0.387  1.00  0.00           C  
HETATM    4  O1  UNL     1       0.801   0.769   1.136  1.00  0.00           O  
HETATM    5  C3  UNL     1       2.865   0.064   0.418  1.00  0.00           C  
HETATM    6  C4  UNL     1       3.727  -0.740  -0.287  1.00  0.00           C  
HETATM    7  C5  UNL     1       5.115  -0.538  -0.221  1.00  0.00           C  
HETATM    8  C6  UNL     1       5.624   0.463   0.548  1.00  0.00           C  
HETATM    9  C7  UNL     1       4.797   1.288   1.268  1.00  0.00           C  
HETATM   10  C8  UNL     1       3.451   1.078   1.193  1.00  0.00           C  
HETATM   11  N2  UNL     1      -0.827  -0.859  -0.077  1.00  0.00           N  
HETATM   12  C9  UNL     1      -1.422  -1.959   0.581  1.00  0.00           C  
HETATM   13  C10 UNL     1      -1.406   0.303  -0.559  1.00  0.00           C  
HETATM   14  O2  UNL     1      -0.605   1.164  -1.137  1.00  0.00           O  
HETATM   15  C11 UNL     1      -2.786   0.751  -0.535  1.00  0.00           C  
HETATM   16  C12 UNL     1      -3.821   0.039   0.018  1.00  0.00           C  
HETATM   17  C13 UNL     1      -5.138   0.482   0.030  1.00  0.00           C  
HETATM   18  C14 UNL     1      -5.418   1.698  -0.543  1.00  0.00           C  
HETATM   19  C15 UNL     1      -4.408   2.442  -1.108  1.00  0.00           C  
HETATM   20  C16 UNL     1      -3.113   1.987  -1.110  1.00  0.00           C  
HETATM   21  H1  UNL     1       1.598  -2.838  -0.702  1.00  0.00           H  
HETATM   22  H2  UNL     1       0.058  -2.532  -1.548  1.00  0.00           H  
HETATM   23  H3  UNL     1       1.522  -1.685  -2.097  1.00  0.00           H  
HETATM   24  H4  UNL     1       3.398  -1.545  -0.910  1.00  0.00           H  
HETATM   25  H5  UNL     1       5.793  -1.180  -0.784  1.00  0.00           H  
HETATM   26  H6  UNL     1       6.681   0.648   0.623  1.00  0.00           H  
HETATM   27  H7  UNL     1       5.220   2.086   1.880  1.00  0.00           H  
HETATM   28  H8  UNL     1       2.773   1.715   1.751  1.00  0.00           H  
HETATM   29  H9  UNL     1      -2.138  -2.550  -0.046  1.00  0.00           H  
HETATM   30  H10 UNL     1      -0.614  -2.753   0.783  1.00  0.00           H  
HETATM   31  H11 UNL     1      -1.840  -1.767   1.591  1.00  0.00           H  
HETATM   32  H12 UNL     1      -3.647  -0.936   0.488  1.00  0.00           H  
HETATM   33  H13 UNL     1      -5.907  -0.128   0.484  1.00  0.00           H  
HETATM   34  H14 UNL     1      -6.430   2.090  -0.560  1.00  0.00           H  
HETATM   35  H15 UNL     1      -4.650   3.416  -1.564  1.00  0.00           H  
HETATM   36  H16 UNL     1      -2.336   2.622  -1.577  1.00  0.00           H  
CONECT    1    2   21   22   23
CONECT    2    3   11
CONECT    3    4    4    5
CONECT    5    6    6   10
CONECT    6    7   24
CONECT    7    8    8   25
CONECT    8    9   26
CONECT    9   10   10   27
CONECT   10   28
CONECT   11   12   13
CONECT   12   29   30   31
CONECT   13   14   14   15
CONECT   15   16   16   20
CONECT   16   17   32
CONECT   17   18   18   33
CONECT   18   19   34
CONECT   19   20   20   35
CONECT   20   36
END

HMDB0255278
     RDKit          3D
N'-Benzoyl-N,N'-dimethylbenzohydrazide
 36 37  0  0  0  0  0  0  0  0999 V2000
    1.0210   -2.0260   -1.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6211   -0.9761   -0.2769 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4434   -0.0950    0.3865 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8008    0.7685    1.1363 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8653    0.0638    0.4184 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7266   -0.7397   -0.2870 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1152   -0.5376   -0.2208 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6235    0.4631    0.5482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7966    1.2875    1.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4505    1.0784    1.1932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8274   -0.8588   -0.0772 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4225   -1.9589    0.5813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4061    0.3032   -0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6053    1.1645   -1.1374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7865    0.7514   -0.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8208    0.0390    0.0183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1376    0.4823    0.0302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4182    1.6983   -0.5429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4083    2.4421   -1.1082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126    1.9872   -1.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5980   -2.8381   -0.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0581   -2.5317   -1.5484 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5220   -1.6853   -2.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3982   -1.5451   -0.9095 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7935   -1.1796   -0.7840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6812    0.6475    0.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2199    2.0857    1.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7727    1.7146    1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1378   -2.5498   -0.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6140   -2.7534    0.7825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8399   -1.7668    1.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6471   -0.9361    0.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9070   -0.1282    0.4836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4303    2.0904   -0.5600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6505    3.4163   -1.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3357    2.6224   -1.5772 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  2 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 10  5  1  0
 20 15  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 12 30  1  0
 12 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 20 36  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Fenoperidine	MeSH
Hydrochloride, phenoperidine	MeSH
Lealgin	MeSH
Operidine	MeSH
Phenoperidine	MeSH
Phenoperidine hydrochloride	MeSH

Chemical Formula

C₁₆H₁₆N₂O₂

Average Molecular Weight

268.316

Monoisotopic Molecular Weight

268.121177763

IUPAC Name

N'-benzoyl-N,N'-dimethylbenzohydrazide

Traditional Name

N'-benzoyl-N,N'-dimethylbenzohydrazide

CAS Registry Number

Not Available

SMILES

CN(N(C)C(=O)C1=CC=CC=C1)C(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C16H16N2O2/c1-17(15(19)13-9-5-3-6-10-13)18(2)16(20)14-11-7-4-8-12-14/h3-12H,1-2H3

InChI Key

PQEZHJRKUSZEBK-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoic acids and derivatives. These are organic compounds containing a carboxylic acid substituent attached to a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Benzoic acids and derivatives

Alternative Parents

Substituents

Benzoic acid or derivatives
Benzoyl
Carboxylic acid hydrazide
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.68	ALOGPS
logP	2.54	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	40.62 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	78.47 m³·mol⁻¹	ChemAxon
Polarizability	27.17 Å³	ChemAxon
Number of Rings	2	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]+	161.426	30932474
DeepCCS	[M-H]-	159.068	30932474
DeepCCS	[M-2H]-	191.954	30932474
DeepCCS	[M+Na]+	167.519	30932474
AllCCS	[M+H]+	164.0	32859911
AllCCS	[M+H-H2O]+	160.3	32859911
AllCCS	[M+NH4]+	167.5	32859911
AllCCS	[M+Na]+	168.5	32859911
AllCCS	[M-H]-	166.8	32859911
AllCCS	[M+Na-2H]-	166.7	32859911
AllCCS	[M+HCOO]-	166.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N'-Benzoyl-N,N'-dimethylbenzohydrazide	CN(N(C)C(=O)C1=CC=CC=C1)C(=O)C1=CC=CC=C1	3100.4	Standard polar	33892256
N'-Benzoyl-N,N'-dimethylbenzohydrazide	CN(N(C)C(=O)C1=CC=CC=C1)C(=O)C1=CC=CC=C1	2153.5	Standard non polar	33892256
N'-Benzoyl-N,N'-dimethylbenzohydrazide	CN(N(C)C(=O)C1=CC=CC=C1)C(=O)C1=CC=CC=C1	2313.4	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 - N'-Benzoyl-N,N'-dimethylbenzohydrazide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-0900000000-2c2d6791adf8904a0ff3	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N'-Benzoyl-N,N'-dimethylbenzohydrazide 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

64202

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71044

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'-Benzoyl-N,N'-dimethylbenzohydrazide (HMDB0255278)

MOL for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

3D MOL for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

3D SDF for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

3D-SDF for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

PDB for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

3D PDB for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

SMILES for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

INCHI for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

Structure for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

3D Structure for HMDB0255278 (N'-Benzoyl-N,N'-dimethylbenzohydrazide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra