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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 22:12:34 UTC

Update Date

2022-09-22 17:44:19 UTC

HMDB ID

HMDB0245105

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2-Diphenylmethylpiperidine

Description

2-Diphenylmethylpiperidine, also known as 2-DPMP or desoxypipradrol, belongs to the class of organic compounds known as diphenylmethanes. Diphenylmethanes are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups. Based on a literature review a small amount of articles have been published on 2-Diphenylmethylpiperidine. This compound has been identified in human blood as reported by (PMID: 31557052 ). 2-diphenylmethylpiperidine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 2-Diphenylmethylpiperidine 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

HMDB0245105
     RDKit          3D
2-Diphenylmethylpiperidine
 40 42  0  0  0  0  0  0  0  0999 V2000
   -3.2674   -2.6487   -0.0672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7358   -2.2602   -1.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6614   -1.3665   -1.2193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1586   -0.8978   -0.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0206    0.0479    0.0314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5621    1.4071   -0.0894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9441    2.0557    1.0676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4638    3.3331    1.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6090    3.9897   -0.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2280    3.3397   -1.2890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7131    2.0776   -1.2933 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0156   -0.3166   -0.9820 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2039    0.6099   -0.9652 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2457    0.2552    0.0372 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5624   -1.2221    0.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2354   -1.9311    0.3470 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3875   -1.6908   -0.8024 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7302   -1.3205    1.1435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7852   -2.1960    1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0978   -3.3366   -0.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1248   -2.6242   -2.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2606   -1.0748   -2.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4836   -0.0266    1.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8468    1.5743    2.0416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7532    3.8076    2.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0211    4.9936   -0.1200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3387    3.8466   -2.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4060    1.5446   -2.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5700   -0.2302   -1.9944 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6750    0.5834   -1.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8484    1.6479   -0.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9080    0.5443    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1727    0.8074   -0.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9153   -1.5948   -0.9166 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2629   -1.3945    0.8839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7983   -1.5608    1.2807 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4403   -3.0200    0.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5557   -2.2878   -0.6940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254   -0.9436    2.0854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2268   -2.5214    2.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  5 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
  4 18  1  0
 18 19  2  0
 19  1  1  0
 11  6  1  0
 17 12  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  0
 19 40  1  0
M  END


  Mrv1652309112100122D          

 19 21  0  0  0  0            999 V2000
    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 N   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
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  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  2  0  0  0  0
  8 13  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0245105

> <DATABASE_NAME>
hmdb

> <SMILES>
C1CCC(NC1)C(C1=CC=CC=C1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H21N/c1-3-9-15(10-4-1)18(16-11-5-2-6-12-16)17-13-7-8-14-19-17/h1-6,9-12,17-19H,7-8,13-14H2

> <INCHI_KEY>
RWTNXJXZVGHMGI-UHFFFAOYSA-N

> <FORMULA>
C18H21N

> <MOLECULAR_WEIGHT>
251.373

> <EXACT_MASS>
251.16739968

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
29.83508942999946

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(diphenylmethyl)piperidine

> <ALOGPS_LOGP>
3.60

> <JCHEM_LOGP>
4.229165851333333

> <ALOGPS_LOGS>
-5.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
10.22217777420198

> <JCHEM_POLAR_SURFACE_AREA>
12.03

> <JCHEM_REFRACTIVITY>
80.43980000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.45e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
desoxypipradrol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0245105
     RDKit          3D
2-Diphenylmethylpiperidine
 40 42  0  0  0  0  0  0  0  0999 V2000
   -3.2674   -2.6487   -0.0672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7358   -2.2602   -1.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6614   -1.3665   -1.2193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1586   -0.8978   -0.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0206    0.0479    0.0314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5621    1.4071   -0.0894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9441    2.0557    1.0676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4638    3.3331    1.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6090    3.9897   -0.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2280    3.3397   -1.2890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7131    2.0776   -1.2933 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0156   -0.3166   -0.9820 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2039    0.6099   -0.9652 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2457    0.2552    0.0372 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5624   -1.2221    0.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2354   -1.9311    0.3470 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3875   -1.6908   -0.8024 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7302   -1.3205    1.1435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7852   -2.1960    1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0978   -3.3366   -0.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1248   -2.6242   -2.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2606   -1.0748   -2.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4836   -0.0266    1.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8468    1.5743    2.0416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7532    3.8076    2.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0211    4.9936   -0.1200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3387    3.8466   -2.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4060    1.5446   -2.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5700   -0.2302   -1.9944 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6750    0.5834   -1.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8484    1.6479   -0.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9080    0.5443    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1727    0.8074   -0.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9153   -1.5948   -0.9166 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2629   -1.3945    0.8839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7983   -1.5608    1.2807 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4403   -3.0200    0.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5557   -2.2878   -0.6940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254   -0.9436    2.0854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2268   -2.5214    2.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  5 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
  4 18  1  0
 18 19  2  0
 19  1  1  0
 11  6  1  0
 17 12  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  0
 19 40  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       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      -2.667  -3.080   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   14                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14    7   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

COMPND    HMDB0245105
HETATM    1  C1  UNL     1      -3.267  -2.649  -0.067  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.736  -2.260  -1.272  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.661  -1.366  -1.219  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.159  -0.898  -0.037  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.021   0.048   0.031  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.562   1.407  -0.089  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.944   2.056   1.068  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.464   3.333   1.057  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.609   3.990  -0.148  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.228   3.340  -1.289  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.713   2.078  -1.293  1.00  0.00           C  
HETATM   12  C12 UNL     1       1.016  -0.317  -0.982  1.00  0.00           C  
HETATM   13  C13 UNL     1       2.204   0.610  -0.965  1.00  0.00           C  
HETATM   14  C14 UNL     1       3.246   0.255   0.037  1.00  0.00           C  
HETATM   15  C15 UNL     1       3.562  -1.222   0.066  1.00  0.00           C  
HETATM   16  C16 UNL     1       2.235  -1.931   0.347  1.00  0.00           C  
HETATM   17  N1  UNL     1       1.387  -1.691  -0.802  1.00  0.00           N  
HETATM   18  C17 UNL     1      -1.730  -1.321   1.143  1.00  0.00           C  
HETATM   19  C18 UNL     1      -2.785  -2.196   1.139  1.00  0.00           C  
HETATM   20  H1  UNL     1      -4.098  -3.337  -0.042  1.00  0.00           H  
HETATM   21  H2  UNL     1      -3.125  -2.624  -2.218  1.00  0.00           H  
HETATM   22  H3  UNL     1      -1.261  -1.075  -2.180  1.00  0.00           H  
HETATM   23  H4  UNL     1       0.484  -0.027   1.030  1.00  0.00           H  
HETATM   24  H5  UNL     1      -0.847   1.574   2.042  1.00  0.00           H  
HETATM   25  H6  UNL     1      -1.753   3.808   2.001  1.00  0.00           H  
HETATM   26  H7  UNL     1      -2.021   4.994  -0.120  1.00  0.00           H  
HETATM   27  H8  UNL     1      -1.339   3.847  -2.233  1.00  0.00           H  
HETATM   28  H9  UNL     1      -0.406   1.545  -2.178  1.00  0.00           H  
HETATM   29  H10 UNL     1       0.570  -0.230  -1.994  1.00  0.00           H  
HETATM   30  H11 UNL     1       2.675   0.583  -1.974  1.00  0.00           H  
HETATM   31  H12 UNL     1       1.848   1.648  -0.738  1.00  0.00           H  
HETATM   32  H13 UNL     1       2.908   0.544   1.049  1.00  0.00           H  
HETATM   33  H14 UNL     1       4.173   0.807  -0.199  1.00  0.00           H  
HETATM   34  H15 UNL     1       3.915  -1.595  -0.917  1.00  0.00           H  
HETATM   35  H16 UNL     1       4.263  -1.395   0.884  1.00  0.00           H  
HETATM   36  H17 UNL     1       1.798  -1.561   1.281  1.00  0.00           H  
HETATM   37  H18 UNL     1       2.440  -3.020   0.381  1.00  0.00           H  
HETATM   38  H19 UNL     1       0.556  -2.288  -0.694  1.00  0.00           H  
HETATM   39  H20 UNL     1      -1.325  -0.944   2.085  1.00  0.00           H  
HETATM   40  H21 UNL     1      -3.227  -2.521   2.078  1.00  0.00           H  
CONECT    1    2    2   19   20
CONECT    2    3   21
CONECT    3    4    4   22
CONECT    4    5   18
CONECT    5    6   12   23
CONECT    6    7    7   11
CONECT    7    8   24
CONECT    8    9    9   25
CONECT    9   10   26
CONECT   10   11   11   27
CONECT   11   28
CONECT   12   13   17   29
CONECT   13   14   30   31
CONECT   14   15   32   33
CONECT   15   16   34   35
CONECT   16   17   36   37
CONECT   17   38
CONECT   18   19   19   39
CONECT   19   40
END

HMDB0245105
     RDKit          3D
2-Diphenylmethylpiperidine
 40 42  0  0  0  0  0  0  0  0999 V2000
   -3.2674   -2.6487   -0.0672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7358   -2.2602   -1.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6614   -1.3665   -1.2193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1586   -0.8978   -0.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0206    0.0479    0.0314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5621    1.4071   -0.0894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9441    2.0557    1.0676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4638    3.3331    1.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6090    3.9897   -0.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2280    3.3397   -1.2890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7131    2.0776   -1.2933 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0156   -0.3166   -0.9820 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2039    0.6099   -0.9652 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2457    0.2552    0.0372 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5624   -1.2221    0.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2354   -1.9311    0.3470 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3875   -1.6908   -0.8024 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7302   -1.3205    1.1435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7852   -2.1960    1.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0978   -3.3366   -0.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1248   -2.6242   -2.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2606   -1.0748   -2.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4836   -0.0266    1.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8468    1.5743    2.0416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7532    3.8076    2.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0211    4.9936   -0.1200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3387    3.8466   -2.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4060    1.5446   -2.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5700   -0.2302   -1.9944 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6750    0.5834   -1.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8484    1.6479   -0.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9080    0.5443    1.0490 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1727    0.8074   -0.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9153   -1.5948   -0.9166 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2629   -1.3945    0.8839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7983   -1.5608    1.2807 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4403   -3.0200    0.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5557   -2.2878   -0.6940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254   -0.9436    2.0854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2268   -2.5214    2.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  5 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
  4 18  1  0
 18 19  2  0
 19  1  1  0
 11  6  1  0
 17 12  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  0
 19 40  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-DPMP	HMDB
2-Diphenylmethylpiperidine hydrochloride, (R)-isomer	HMDB
2-Diphenylmethylpiperidine hydrochloride, (S)-isomer	HMDB
2-Diphenylmethylpiperidine, (R)-isomer	HMDB
2-Diphenylmethylpiperidine, (S)-isomer	HMDB
Desoxypipradrol	HMDB

Chemical Formula

C₁₈H₂₁N

Average Molecular Weight

251.373

Monoisotopic Molecular Weight

251.16739968

IUPAC Name

2-(diphenylmethyl)piperidine

Traditional Name

desoxypipradrol

CAS Registry Number

Not Available

SMILES

C1CCC(NC1)C(C1=CC=CC=C1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C18H21N/c1-3-9-15(10-4-1)18(16-11-5-2-6-12-16)17-13-7-8-14-19-17/h1-6,9-12,17-19H,7-8,13-14H2

InChI Key

RWTNXJXZVGHMGI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diphenylmethanes. Diphenylmethanes are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Diphenylmethanes

Direct Parent

Diphenylmethanes

Alternative Parents

Substituents

Diphenylmethane
Aralkylamine
Piperidine
Azacycle
Organoheterocyclic compound
Secondary amine
Secondary aliphatic amine
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
Amine
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	3.6	ALOGPS
logP	4.23	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Basic)	10.22	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	12.03 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	80.44 m³·mol⁻¹	ChemAxon
Polarizability	29.84 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	161.481	30932474
DeepCCS	[M-H]-	159.123	30932474
DeepCCS	[M-2H]-	192.008	30932474
DeepCCS	[M+Na]+	167.574	30932474
AllCCS	[M+H]+	161.6	32859911
AllCCS	[M+H-H2O]+	157.7	32859911
AllCCS	[M+NH4]+	165.3	32859911
AllCCS	[M+Na]+	166.3	32859911
AllCCS	[M-H]-	168.8	32859911
AllCCS	[M+Na-2H]-	168.6	32859911
AllCCS	[M+HCOO]-	168.5	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	11.6065 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.78 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1306.5 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	283.3 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	170.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	181.0 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	114.6 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	393.0 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	404.7 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	337.2 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1138.3 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	397.8 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	950.3 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	269.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	316.4 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	391.7 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	335.9 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	10.1 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2-Diphenylmethylpiperidine	C1CCC(NC1)C(C1=CC=CC=C1)C1=CC=CC=C1	2609.5	Standard polar	33892256
2-Diphenylmethylpiperidine	C1CCC(NC1)C(C1=CC=CC=C1)C1=CC=CC=C1	2067.2	Standard non polar	33892256
2-Diphenylmethylpiperidine	C1CCC(NC1)C(C1=CC=CC=C1)C1=CC=CC=C1	2059.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-Diphenylmethylpiperidine,1TMS,isomer #1	C[Si](C)(C)N1CCCCC1C(C1=CC=CC=C1)C1=CC=CC=C1	2066.6	Semi standard non polar	33892256
2-Diphenylmethylpiperidine,1TMS,isomer #1	C[Si](C)(C)N1CCCCC1C(C1=CC=CC=C1)C1=CC=CC=C1	2180.1	Standard non polar	33892256
2-Diphenylmethylpiperidine,1TMS,isomer #1	C[Si](C)(C)N1CCCCC1C(C1=CC=CC=C1)C1=CC=CC=C1	2855.5	Standard polar	33892256
2-Diphenylmethylpiperidine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N1CCCCC1C(C1=CC=CC=C1)C1=CC=CC=C1	2302.3	Semi standard non polar	33892256
2-Diphenylmethylpiperidine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N1CCCCC1C(C1=CC=CC=C1)C1=CC=CC=C1	2335.1	Standard non polar	33892256
2-Diphenylmethylpiperidine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N1CCCCC1C(C1=CC=CC=C1)C1=CC=CC=C1	2976.4	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Diphenylmethylpiperidine GC-MS (Non-derivatized) - 70eV, Positive	splash10-001i-9210000000-3e00fa1d40b52d28edbb	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Diphenylmethylpiperidine 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 - 2-Diphenylmethylpiperidine 10V, Positive-QTOF	splash10-0udi-0090000000-2d425712ed3d5dfa5170	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Diphenylmethylpiperidine 20V, Positive-QTOF	splash10-0udi-0490000000-a1cd8dcd723dba07bc79	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Diphenylmethylpiperidine 40V, Positive-QTOF	splash10-014i-2910000000-c48d0e37510da6e77faf	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Diphenylmethylpiperidine 10V, Negative-QTOF	splash10-0udi-0090000000-b6b92119f58619477a56	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Diphenylmethylpiperidine 20V, Negative-QTOF	splash10-0uxr-1590000000-8567917ef24c78a9a90b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Diphenylmethylpiperidine 40V, Negative-QTOF	splash10-014i-1900000000-be6eff5648b8e2d84640	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Urine

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

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Urine	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details

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

141045

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Desoxypipradrol

METLIN ID

Not Available

PubChem Compound

160506

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 2-Diphenylmethylpiperidine (HMDB0245105)

MOL for HMDB0245105 (2-Diphenylmethylpiperidine)

3D MOL for HMDB0245105 (2-Diphenylmethylpiperidine)

3D SDF for HMDB0245105 (2-Diphenylmethylpiperidine)

3D-SDF for HMDB0245105 (2-Diphenylmethylpiperidine)

PDB for HMDB0245105 (2-Diphenylmethylpiperidine)

3D PDB for HMDB0245105 (2-Diphenylmethylpiperidine)

SMILES for HMDB0245105 (2-Diphenylmethylpiperidine)

INCHI for HMDB0245105 (2-Diphenylmethylpiperidine)

Structure for HMDB0245105 (2-Diphenylmethylpiperidine)

3D Structure for HMDB0245105 (2-Diphenylmethylpiperidine)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra