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

2021-09-10 23:34:54 UTC

Update Date

2021-09-26 22:55:44 UTC

HMDB ID

HMDB0246565

Secondary Accession Numbers

None

Metabolite Identification

Common Name

4-P-Pdot

Description

4-P-Pdot, also known as 4P-PDOT, belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane. Based on a literature review a significant number of articles have been published on 4-P-Pdot. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4-p-pdot is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4-P-Pdot 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

HMDB0246565
     RDKit          3D
4-P-Pdot
 42 44  0  0  0  0  0  0  0  0999 V2000
    6.0022    0.9540   -0.7280 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9141    0.6564    0.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    0.3663   -0.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6628    0.4014   -1.7019 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4419    0.0452    0.2040 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2652   -0.2244   -0.5844 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9322   -1.6790   -0.3873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4728   -2.0265   -0.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8251   -3.2023   -1.2259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1827   -3.4589   -1.3847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1600   -2.5927   -0.9417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8013   -1.4111   -0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4684   -1.1681   -0.1581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656    0.0815    0.5112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0514    0.9975    0.8252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5065    1.9888   -0.0216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5395    2.8195    0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1602    2.6928    1.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7294    1.7136    2.4350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6914    0.8930    2.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1359    0.7045   -0.3068 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7538    0.4625   -1.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0019    0.6363   -0.3539 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0441    2.0524   -0.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2237   -0.2763    0.8177 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7654    1.4669    1.0021 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4455    0.0167    1.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5510   -0.1234   -1.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2331   -1.9658    0.6523 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5525   -2.2959   -1.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0720   -3.8926   -1.5793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4972   -4.3699   -1.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2204   -2.7695   -1.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5236   -0.6953    0.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5027   -0.2549    1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0213    2.0834   -0.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8814    3.5894   -0.3351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9843    3.3499    1.8662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2227    1.6181    3.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3823    0.1362    2.7569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2506    1.1145   -1.2553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5241    1.5658    0.2803 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  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 14 21  1  0
 21  6  1  0
 13  8  1  0
 20 15  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  5 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 14 35  1  0
 16 36  1  0
 17 37  1  0
 18 38  1  0
 19 39  1  0
 20 40  1  0
 21 41  1  0
 21 42  1  0
M  END

  Mrv1652309112101352D          

 21 23  0  0  0  0            999 V2000
   -0.7145   -3.7125    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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -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
    0.7145   -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
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    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   -1.6500    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
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    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
    2.1434    2.0625    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  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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 15  1  0  0  0  0
  8 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
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0246565

> <DATABASE_NAME>
hmdb

> <SMILES>
CCC(=O)NC1CC(C2=CC=CC=C2)C2=CC=CC=C2C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H21NO/c1-2-19(21)20-16-12-15-10-6-7-11-17(15)18(13-16)14-8-4-3-5-9-14/h3-11,16,18H,2,12-13H2,1H3,(H,20,21)

> <INCHI_KEY>
RCYLUNPFECYGDW-UHFFFAOYSA-N

> <FORMULA>
C19H21NO

> <MOLECULAR_WEIGHT>
279.383

> <EXACT_MASS>
279.1623143

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
32.373744289064916

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-(4-phenyl-1,2,3,4-tetrahydronaphthalen-2-yl)propanamide

> <ALOGPS_LOGP>
3.91

> <JCHEM_LOGP>
3.8721052173333335

> <ALOGPS_LOGS>
-5.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.923255477450194

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2687514105539792

> <JCHEM_POLAR_SURFACE_AREA>
29.1

> <JCHEM_REFRACTIVITY>
85.58150000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.13e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-(4-phenyl-1,2,3,4-tetrahydronaphthalen-2-yl)propanamide

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0246565
     RDKit          3D
4-P-Pdot
 42 44  0  0  0  0  0  0  0  0999 V2000
    6.0022    0.9540   -0.7280 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9141    0.6564    0.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    0.3663   -0.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6628    0.4014   -1.7019 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4419    0.0452    0.2040 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2652   -0.2244   -0.5844 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9322   -1.6790   -0.3873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4728   -2.0265   -0.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8251   -3.2023   -1.2259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1827   -3.4589   -1.3847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1600   -2.5927   -0.9417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8013   -1.4111   -0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4684   -1.1681   -0.1581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656    0.0815    0.5112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0514    0.9975    0.8252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5065    1.9888   -0.0216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5395    2.8195    0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1602    2.6928    1.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7294    1.7136    2.4350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6914    0.8930    2.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1359    0.7045   -0.3068 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7538    0.4625   -1.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0019    0.6363   -0.3539 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0441    2.0524   -0.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2237   -0.2763    0.8177 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7654    1.4669    1.0021 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4455    0.0167    1.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5510   -0.1234   -1.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2331   -1.9658    0.6523 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5525   -2.2959   -1.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0720   -3.8926   -1.5793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4972   -4.3699   -1.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2204   -2.7695   -1.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5236   -0.6953    0.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5027   -0.2549    1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0213    2.0834   -0.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8814    3.5894   -0.3351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9843    3.3499    1.8662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2227    1.6181    3.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3823    0.1362    2.7569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2506    1.1145   -1.2553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5241    1.5658    0.2803 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  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 14 21  1  0
 21  6  1  0
 13  8  1  0
 20 15  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  5 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 14 35  1  0
 16 36  1  0
 17 37  1  0
 18 38  1  0
 19 39  1  0
 20 40  1  0
 21 41  1  0
 21 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      -1.334  -6.930   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       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       0.000  -3.080   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       1.334  -2.310   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       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14    6                                                       
CONECT   16    8   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

COMPND    HMDB0246711
HETATM    1  C1  UNL     1       6.210   0.183  -0.764  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.975   0.200   0.099  1.00  0.00           C  
HETATM    3  C3  UNL     1       3.723  -0.006  -0.748  1.00  0.00           C  
HETATM    4  O1  UNL     1       3.981   0.035  -1.986  1.00  0.00           O  
HETATM    5  N1  UNL     1       2.508  -0.211  -0.172  1.00  0.00           N  
HETATM    6  C4  UNL     1       1.276  -0.418   0.412  1.00  0.00           C  
HETATM    7  C5  UNL     1       0.804  -1.840   0.396  1.00  0.00           C  
HETATM    8  C6  UNL     1      -0.648  -2.012   0.444  1.00  0.00           C  
HETATM    9  C7  UNL     1      -1.152  -3.341   0.395  1.00  0.00           C  
HETATM   10  C8  UNL     1      -2.500  -3.561   0.430  1.00  0.00           C  
HETATM   11  C9  UNL     1      -3.362  -2.491   0.511  1.00  0.00           C  
HETATM   12  C10 UNL     1      -2.873  -1.207   0.558  1.00  0.00           C  
HETATM   13  C11 UNL     1      -1.521  -0.970   0.524  1.00  0.00           C  
HETATM   14  C12 UNL     1      -1.037   0.432   0.573  1.00  0.00           C  
HETATM   15  C13 UNL     1      -2.005   1.447   0.185  1.00  0.00           C  
HETATM   16  C14 UNL     1      -2.840   2.001   1.161  1.00  0.00           C  
HETATM   17  C15 UNL     1      -3.783   2.954   0.886  1.00  0.00           C  
HETATM   18  C16 UNL     1      -3.934   3.403  -0.408  1.00  0.00           C  
HETATM   19  C17 UNL     1      -3.132   2.890  -1.427  1.00  0.00           C  
HETATM   20  C18 UNL     1      -2.193   1.925  -1.088  1.00  0.00           C  
HETATM   21  C19 UNL     1       0.243   0.550  -0.206  1.00  0.00           C  
HETATM   22  H1  UNL     1       6.931   0.982  -0.490  1.00  0.00           H  
HETATM   23  H2  UNL     1       6.746  -0.809  -0.690  1.00  0.00           H  
HETATM   24  H3  UNL     1       5.951   0.251  -1.855  1.00  0.00           H  
HETATM   25  H4  UNL     1       4.932   1.108   0.689  1.00  0.00           H  
HETATM   26  H5  UNL     1       5.014  -0.699   0.754  1.00  0.00           H  
HETATM   27  H6  UNL     1       1.936  -0.429  -1.394  1.00  0.00           H  
HETATM   28  H7  UNL     1       1.277  -0.142   1.542  1.00  0.00           H  
HETATM   29  H8  UNL     1       1.202  -2.361  -0.546  1.00  0.00           H  
HETATM   30  H9  UNL     1       1.296  -2.390   1.239  1.00  0.00           H  
HETATM   31  H10 UNL     1      -0.434  -4.156   0.337  1.00  0.00           H  
HETATM   32  H11 UNL     1      -2.889  -4.594   0.401  1.00  0.00           H  
HETATM   33  H12 UNL     1      -4.426  -2.687   0.538  1.00  0.00           H  
HETATM   34  H13 UNL     1      -3.567  -0.389   0.615  1.00  0.00           H  
HETATM   35  H14 UNL     1      -0.751   0.600   1.643  1.00  0.00           H  
HETATM   36  H15 UNL     1      -2.758   1.678   2.205  1.00  0.00           H  
HETATM   37  H16 UNL     1      -4.443   3.386   1.659  1.00  0.00           H  
HETATM   38  H17 UNL     1      -4.665   4.156  -0.664  1.00  0.00           H  
HETATM   39  H18 UNL     1      -3.289   3.270  -2.419  1.00  0.00           H  
HETATM   40  H19 UNL     1      -1.560   1.521  -1.903  1.00  0.00           H  
HETATM   41  H20 UNL     1       0.099   0.207  -1.241  1.00  0.00           H  
HETATM   42  H21 UNL     1       0.660   1.533  -0.196  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3   25   26
CONECT    3    4    4    5
CONECT    5    6   27
CONECT    6    7   21   28
CONECT    7    8   29   30
CONECT    8    9    9   13
CONECT    9   10   31
CONECT   10   11   11   32
CONECT   11   12   33
CONECT   12   13   13   34
CONECT   13   14
CONECT   14   15   21   35
CONECT   15   16   16   20
CONECT   16   17   36
CONECT   17   18   18   37
CONECT   18   19   38
CONECT   19   20   20   39
CONECT   20   40
CONECT   21   41   42
END

HMDB0246565
     RDKit          3D
4-P-Pdot
 42 44  0  0  0  0  0  0  0  0999 V2000
    6.0022    0.9540   -0.7280 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9141    0.6564    0.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    0.3663   -0.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6628    0.4014   -1.7019 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4419    0.0452    0.2040 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2652   -0.2244   -0.5844 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9322   -1.6790   -0.3873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4728   -2.0265   -0.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8251   -3.2023   -1.2259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1827   -3.4589   -1.3847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1600   -2.5927   -0.9417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8013   -1.4111   -0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4684   -1.1681   -0.1581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656    0.0815    0.5112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0514    0.9975    0.8252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5065    1.9888   -0.0216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5395    2.8195    0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1602    2.6928    1.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7294    1.7136    2.4350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6914    0.8930    2.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1359    0.7045   -0.3068 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7538    0.4625   -1.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0019    0.6363   -0.3539 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0441    2.0524   -0.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2237   -0.2763    0.8177 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7654    1.4669    1.0021 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4455    0.0167    1.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5510   -0.1234   -1.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2331   -1.9658    0.6523 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5525   -2.2959   -1.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0720   -3.8926   -1.5793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4972   -4.3699   -1.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2204   -2.7695   -1.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5236   -0.6953    0.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5027   -0.2549    1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0213    2.0834   -0.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8814    3.5894   -0.3351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9843    3.3499    1.8662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2227    1.6181    3.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3823    0.1362    2.7569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2506    1.1145   -1.2553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5241    1.5658    0.2803 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  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 14 21  1  0
 21  6  1  0
 13  8  1  0
 20 15  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  5 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  9 31  1  0
 10 32  1  0
 11 33  1  0
 12 34  1  0
 14 35  1  0
 16 36  1  0
 17 37  1  0
 18 38  1  0
 19 39  1  0
 20 40  1  0
 21 41  1  0
 21 42  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
N-(4-Phenyl-1,2,3,4-tetrahydronaphthalen-2-yl)propanimidate	HMDB
4-Phenyl-2-propionamidotetraline	HMDB
4P-PDOT	HMDB

Chemical Formula

C₁₉H₂₁NO

Average Molecular Weight

279.383

Monoisotopic Molecular Weight

279.1623143

IUPAC Name

N-(4-phenyl-1,2,3,4-tetrahydronaphthalen-2-yl)propanamide

Traditional Name

N-(4-phenyl-1,2,3,4-tetrahydronaphthalen-2-yl)propanamide

CAS Registry Number

Not Available

SMILES

CCC(=O)NC1CC(C2=CC=CC=C2)C2=CC=CC=C2C1

InChI Identifier

InChI=1S/C19H21NO/c1-2-19(21)20-16-12-15-10-6-7-11-17(15)18(13-16)14-8-4-3-5-9-14/h3-11,16,18H,2,12-13H2,1H3,(H,20,21)

InChI Key

RCYLUNPFECYGDW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Tetralins

Sub Class

Not Available

Direct Parent

Tetralins

Alternative Parents

Substituents

Tetralin
Monocyclic benzene moiety
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	3.91	ALOGPS
logP	3.87	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	15.92	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.1 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	85.58 m³·mol⁻¹	ChemAxon
Polarizability	32.37 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]+	162.88	30932474
DeepCCS	[M-H]-	160.522	30932474
DeepCCS	[M-2H]-	193.407	30932474
DeepCCS	[M+Na]+	168.973	30932474
AllCCS	[M+H]+	169.1	32859911
AllCCS	[M+H-H2O]+	165.6	32859911
AllCCS	[M+NH4]+	172.4	32859911
AllCCS	[M+Na]+	173.4	32859911
AllCCS	[M-H]-	174.6	32859911
AllCCS	[M+Na-2H]-	174.3	32859911
AllCCS	[M+HCOO]-	174.1	32859911

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4-P-Pdot,1TMS,isomer #1	CCC(=O)N(C1CC2=CC=CC=C2C(C2=CC=CC=C2)C1)[Si](C)(C)C	2420.2	Semi standard non polar	33892256
4-P-Pdot,1TMS,isomer #1	CCC(=O)N(C1CC2=CC=CC=C2C(C2=CC=CC=C2)C1)[Si](C)(C)C	2529.9	Standard non polar	33892256
4-P-Pdot,1TMS,isomer #1	CCC(=O)N(C1CC2=CC=CC=C2C(C2=CC=CC=C2)C1)[Si](C)(C)C	3090.1	Standard polar	33892256
4-P-Pdot,1TBDMS,isomer #1	CCC(=O)N(C1CC2=CC=CC=C2C(C2=CC=CC=C2)C1)[Si](C)(C)C(C)(C)C	2656.6	Semi standard non polar	33892256
4-P-Pdot,1TBDMS,isomer #1	CCC(=O)N(C1CC2=CC=CC=C2C(C2=CC=CC=C2)C1)[Si](C)(C)C(C)(C)C	2814.1	Standard non polar	33892256
4-P-Pdot,1TBDMS,isomer #1	CCC(=O)N(C1CC2=CC=CC=C2C(C2=CC=CC=C2)C1)[Si](C)(C)C(C)(C)C	3155.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 4-P-Pdot GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-6390000000-7e855c9eca472f8ffd7b	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-P-Pdot GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-P-Pdot GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-P-Pdot 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-P-Pdot 10V, Positive-QTOF	splash10-00e9-0190000000-7ac59f3ef3407fd43c7e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-P-Pdot 20V, Positive-QTOF	splash10-05fs-0690000000-9ac4dd4266bf7df976e1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-P-Pdot 40V, Positive-QTOF	splash10-0a7l-4930000000-6307515f3ebbe03b65a1	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-P-Pdot 10V, Negative-QTOF	splash10-00di-0090000000-249adcb5d935f5e65465	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-P-Pdot 20V, Negative-QTOF	splash10-0006-9050000000-31d75b65aeb45fca5479	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-P-Pdot 40V, Negative-QTOF	splash10-002f-9530000000-6928878c399b2daf2beb	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

3195800

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3976006

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-P-Pdot (HMDB0246565)

MOL for HMDB0246565 (4-P-Pdot)

3D MOL for HMDB0246565 (4-P-Pdot)

3D SDF for HMDB0246565 (4-P-Pdot)

3D-SDF for HMDB0246565 (4-P-Pdot)

PDB for HMDB0246565 (4-P-Pdot)

3D PDB for HMDB0246565 (4-P-Pdot)

SMILES for HMDB0246565 (4-P-Pdot)

INCHI for HMDB0246565 (4-P-Pdot)

Structure for HMDB0246565 (4-P-Pdot)

3D Structure for HMDB0246565 (4-P-Pdot)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra