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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 06:55:59 UTC

Update Date

2021-09-26 23:01:08 UTC

HMDB ID

HMDB0249967

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Nor-cocaine

Description

Nor-cocaine belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. Based on a literature review a small amount of articles have been published on Nor-cocaine. This compound has been identified in human blood as reported by (PMID: 31557052 ). Nor-cocaine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Nor-cocaine 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

HMDB0249967
     RDKit          3D
Nor-cocaine
 40 42  0  0  0  0  0  0  0  0999 V2000
   -2.2263   -3.6461   -0.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1940   -2.3987    0.6330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4064   -1.3406    0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6691   -1.4714   -0.7547 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3997   -0.0309    0.9767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8423    0.4832    0.8966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8825    1.8868    1.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9599    2.7568    0.1891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4299    1.8100   -0.8709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9498    1.7430   -0.7496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4343    0.9379    0.4002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7561    0.2422    0.0184 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866    0.5009    0.6027 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0078    1.3862    1.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2055   -0.1818    0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1877   -1.1484   -0.7307 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3682   -1.8148   -1.0857 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5635   -1.4959   -0.4503 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5703   -0.5146    0.5339 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3892    0.1214    0.8583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1127    0.5919   -0.5465 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2907   -3.8916   -0.5503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0638   -3.7399   -0.7428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3689   -4.4446    0.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2118   -0.1926    2.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5056   -0.2176    1.3952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7469    2.0430    2.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9500    2.1415    1.9882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3299    3.6643    0.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0135    2.9869   -0.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6829    2.1843   -1.8816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5540    1.2840   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5557    2.7818   -0.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1317    1.6557    1.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2988   -1.4340   -1.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3278   -2.5698   -1.8522 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4770   -2.0153   -0.7286 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5028   -0.2927    1.0028 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4074    0.8810    1.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1365    0.7584   -0.6828 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  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 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
  9 21  1  0
 11  5  1  0
 20 15  1  0
 21  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
  7 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 16 35  1  0
 17 36  1  0
 18 37  1  0
 19 38  1  0
 20 39  1  0
 21 40  1  0
M  END

  Mrv1652309112108562D          

 21 23  0  0  0  0            999 V2000
    4.0616    0.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    1.4540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9444    1.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6430    2.3449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4300    0.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257    1.1155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807    0.6012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807   -0.2238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257   -0.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3940    0.1887    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4300   -0.5546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880    0.1887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130    0.1887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0255   -0.5258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8505   -0.5258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130   -1.2403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0255   -1.9548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130   -2.6692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880   -2.6692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3755   -1.9548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880   -1.2403    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  1  0  0  0  0
  6 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 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>
HMDB0249967

> <DATABASE_NAME>
hmdb

> <SMILES>
COC(=O)C1C2CCC(CC1OC(=O)C1=CC=CC=C1)N2

> <INCHI_IDENTIFIER>
InChI=1S/C16H19NO4/c1-20-16(19)14-12-8-7-11(17-12)9-13(14)21-15(18)10-5-3-2-4-6-10/h2-6,11-14,17H,7-9H2,1H3

> <INCHI_KEY>
AYDBLCSLKNTEJL-UHFFFAOYSA-N

> <FORMULA>
C16H19NO4

> <MOLECULAR_WEIGHT>
289.331

> <EXACT_MASS>
289.131408096

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
30.295064064002624

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 3-(benzoyloxy)-8-azabicyclo[3.2.1]octane-2-carboxylate

> <ALOGPS_LOGP>
0.51

> <JCHEM_LOGP>
1.899060071666666

> <ALOGPS_LOGS>
-2.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.964081165344764

> <JCHEM_POLAR_SURFACE_AREA>
64.63

> <JCHEM_REFRACTIVITY>
75.86570000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.28e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3-(benzoyloxy)-8-azabicyclo[3.2.1]octane-2-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0249967
     RDKit          3D
Nor-cocaine
 40 42  0  0  0  0  0  0  0  0999 V2000
   -2.2263   -3.6461   -0.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1940   -2.3987    0.6330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4064   -1.3406    0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6691   -1.4714   -0.7547 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3997   -0.0309    0.9767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8423    0.4832    0.8966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8825    1.8868    1.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9599    2.7568    0.1891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4299    1.8100   -0.8709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9498    1.7430   -0.7496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4343    0.9379    0.4002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7561    0.2422    0.0184 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866    0.5009    0.6027 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0078    1.3862    1.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2055   -0.1818    0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1877   -1.1484   -0.7307 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3682   -1.8148   -1.0857 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5635   -1.4959   -0.4503 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5703   -0.5146    0.5339 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3892    0.1214    0.8583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1127    0.5919   -0.5465 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2907   -3.8916   -0.5503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0638   -3.7399   -0.7428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3689   -4.4446    0.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2118   -0.1926    2.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5056   -0.2176    1.3952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7469    2.0430    2.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9500    2.1415    1.9882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3299    3.6643    0.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0135    2.9869   -0.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6829    2.1843   -1.8816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5540    1.2840   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5557    2.7818   -0.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1317    1.6557    1.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2988   -1.4340   -1.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3278   -2.5698   -1.8522 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4770   -2.0153   -0.7286 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5028   -0.2927    1.0028 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4074    0.8810    1.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1365    0.7584   -0.6828 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  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 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
  9 21  1  0
 11  5  1  0
 20 15  1  0
 21  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
  7 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 16 35  1  0
 17 36  1  0
 18 37  1  0
 19 38  1  0
 20 39  1  0
 21 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       7.582   1.281   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.019   2.714   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.496   2.944   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.934   4.377   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.536   1.740   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.035   2.082   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.831   1.122   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.831  -0.418   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.035  -1.378   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       2.602   0.352   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       4.536  -1.035   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.204   0.352   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.744   0.352   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.514  -0.982   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.054  -0.982   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.744  -2.315   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.514  -3.649   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.744  -4.983   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.204  -4.983   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.434  -3.649   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.204  -2.315   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   12                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9    6                                                       
CONECT   11    9   12                                                       
CONECT   12   11    5   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   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    HMDB0249967
HETATM    1  C1  UNL     1      -2.226  -3.646  -0.032  1.00  0.00           C  
HETATM    2  O1  UNL     1      -2.194  -2.399   0.633  1.00  0.00           O  
HETATM    3  C2  UNL     1      -1.406  -1.341   0.244  1.00  0.00           C  
HETATM    4  O2  UNL     1      -0.669  -1.471  -0.755  1.00  0.00           O  
HETATM    5  C3  UNL     1      -1.400  -0.031   0.977  1.00  0.00           C  
HETATM    6  C4  UNL     1      -2.842   0.483   0.897  1.00  0.00           C  
HETATM    7  C5  UNL     1      -2.883   1.887   1.426  1.00  0.00           C  
HETATM    8  C6  UNL     1      -2.960   2.757   0.189  1.00  0.00           C  
HETATM    9  C7  UNL     1      -2.430   1.810  -0.871  1.00  0.00           C  
HETATM   10  C8  UNL     1      -0.950   1.743  -0.750  1.00  0.00           C  
HETATM   11  C9  UNL     1      -0.434   0.938   0.400  1.00  0.00           C  
HETATM   12  O3  UNL     1       0.756   0.242   0.018  1.00  0.00           O  
HETATM   13  C10 UNL     1       1.987   0.501   0.603  1.00  0.00           C  
HETATM   14  O4  UNL     1       2.008   1.386   1.495  1.00  0.00           O  
HETATM   15  C11 UNL     1       3.205  -0.182   0.242  1.00  0.00           C  
HETATM   16  C12 UNL     1       3.188  -1.148  -0.731  1.00  0.00           C  
HETATM   17  C13 UNL     1       4.368  -1.815  -1.086  1.00  0.00           C  
HETATM   18  C14 UNL     1       5.563  -1.496  -0.450  1.00  0.00           C  
HETATM   19  C15 UNL     1       5.570  -0.515   0.534  1.00  0.00           C  
HETATM   20  C16 UNL     1       4.389   0.121   0.858  1.00  0.00           C  
HETATM   21  N1  UNL     1      -3.113   0.592  -0.546  1.00  0.00           N  
HETATM   22  H1  UNL     1      -1.291  -3.892  -0.550  1.00  0.00           H  
HETATM   23  H2  UNL     1      -3.064  -3.740  -0.743  1.00  0.00           H  
HETATM   24  H3  UNL     1      -2.369  -4.445   0.749  1.00  0.00           H  
HETATM   25  H4  UNL     1      -1.212  -0.193   2.067  1.00  0.00           H  
HETATM   26  H5  UNL     1      -3.506  -0.218   1.395  1.00  0.00           H  
HETATM   27  H6  UNL     1      -3.747   2.043   2.100  1.00  0.00           H  
HETATM   28  H7  UNL     1      -1.950   2.142   1.988  1.00  0.00           H  
HETATM   29  H8  UNL     1      -2.330   3.664   0.282  1.00  0.00           H  
HETATM   30  H9  UNL     1      -4.014   2.987  -0.082  1.00  0.00           H  
HETATM   31  H10 UNL     1      -2.683   2.184  -1.882  1.00  0.00           H  
HETATM   32  H11 UNL     1      -0.554   1.284  -1.698  1.00  0.00           H  
HETATM   33  H12 UNL     1      -0.556   2.782  -0.742  1.00  0.00           H  
HETATM   34  H13 UNL     1      -0.132   1.656   1.199  1.00  0.00           H  
HETATM   35  H14 UNL     1       2.299  -1.434  -1.252  1.00  0.00           H  
HETATM   36  H15 UNL     1       4.328  -2.570  -1.852  1.00  0.00           H  
HETATM   37  H16 UNL     1       6.477  -2.015  -0.729  1.00  0.00           H  
HETATM   38  H17 UNL     1       6.503  -0.293   1.003  1.00  0.00           H  
HETATM   39  H18 UNL     1       4.407   0.881   1.624  1.00  0.00           H  
HETATM   40  H19 UNL     1      -4.136   0.758  -0.683  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3
CONECT    3    4    4    5
CONECT    5    6   11   25
CONECT    6    7   21   26
CONECT    7    8   27   28
CONECT    8    9   29   30
CONECT    9   10   21   31
CONECT   10   11   32   33
CONECT   11   12   34
CONECT   12   13
CONECT   13   14   14   15
CONECT   15   16   16   20
CONECT   16   17   35
CONECT   17   18   18   36
CONECT   18   19   37
CONECT   19   20   20   38
CONECT   20   39
CONECT   21   40
END

HMDB0249967
     RDKit          3D
Nor-cocaine
 40 42  0  0  0  0  0  0  0  0999 V2000
   -2.2263   -3.6461   -0.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1940   -2.3987    0.6330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4064   -1.3406    0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6691   -1.4714   -0.7547 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3997   -0.0309    0.9767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8423    0.4832    0.8966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8825    1.8868    1.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9599    2.7568    0.1891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4299    1.8100   -0.8709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9498    1.7430   -0.7496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4343    0.9379    0.4002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7561    0.2422    0.0184 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866    0.5009    0.6027 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0078    1.3862    1.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2055   -0.1818    0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1877   -1.1484   -0.7307 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3682   -1.8148   -1.0857 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5635   -1.4959   -0.4503 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5703   -0.5146    0.5339 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3892    0.1214    0.8583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1127    0.5919   -0.5465 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2907   -3.8916   -0.5503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0638   -3.7399   -0.7428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3689   -4.4446    0.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2118   -0.1926    2.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5056   -0.2176    1.3952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7469    2.0430    2.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9500    2.1415    1.9882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3299    3.6643    0.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0135    2.9869   -0.0822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6829    2.1843   -1.8816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5540    1.2840   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5557    2.7818   -0.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1317    1.6557    1.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2988   -1.4340   -1.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3278   -2.5698   -1.8522 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4770   -2.0153   -0.7286 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5028   -0.2927    1.0028 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4074    0.8810    1.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1365    0.7584   -0.6828 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  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 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
  9 21  1  0
 11  5  1  0
 20 15  1  0
 21  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
  7 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 16 35  1  0
 17 36  1  0
 18 37  1  0
 19 38  1  0
 20 39  1  0
 21 40  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₆H₁₉NO₄

Average Molecular Weight

289.331

Monoisotopic Molecular Weight

289.131408096

IUPAC Name

methyl 3-(benzoyloxy)-8-azabicyclo[3.2.1]octane-2-carboxylate

Traditional Name

methyl 3-(benzoyloxy)-8-azabicyclo[3.2.1]octane-2-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1C2CCC(CC1OC(=O)C1=CC=CC=C1)N2

InChI Identifier

InChI=1S/C16H19NO4/c1-20-16(19)14-12-8-7-11(17-12)9-13(14)21-15(18)10-5-3-2-4-6-10/h2-6,11-14,17H,7-9H2,1H3

InChI Key

AYDBLCSLKNTEJL-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Benzoic acid esters

Alternative Parents

Substituents

Benzoate ester
Piperidinecarboxylic acid
Tropane alkaloid
Benzoyl
Dicarboxylic acid or derivatives
Piperidine
Methyl ester
Pyrrolidine
Amino acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Secondary aliphatic amine
Azacycle
Organoheterocyclic compound
Secondary amine
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Amine
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	0.51	ALOGPS
logP	1.9	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Basic)	9.96	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.63 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	75.87 m³·mol⁻¹	ChemAxon
Polarizability	30.3 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	167.237	30932474
DeepCCS	[M-H]-	164.879	30932474
DeepCCS	[M-2H]-	197.765	30932474
DeepCCS	[M+Na]+	173.33	30932474
AllCCS	[M+H]+	169.3	32859911
AllCCS	[M+H-H2O]+	166.0	32859911
AllCCS	[M+NH4]+	172.4	32859911
AllCCS	[M+Na]+	173.3	32859911
AllCCS	[M-H]-	169.2	32859911
AllCCS	[M+Na-2H]-	169.0	32859911
AllCCS	[M+HCOO]-	168.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Nor-cocaine	COC(=O)C1C2CCC(CC1OC(=O)C1=CC=CC=C1)N2	3169.7	Standard polar	33892256
Nor-cocaine	COC(=O)C1C2CCC(CC1OC(=O)C1=CC=CC=C1)N2	2369.0	Standard non polar	33892256
Nor-cocaine	COC(=O)C1C2CCC(CC1OC(=O)C1=CC=CC=C1)N2	2326.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Nor-cocaine,1TMS,isomer #1	COC(=O)C1C(OC(=O)C2=CC=CC=C2)CC2CCC1N2[Si](C)(C)C	2265.3	Semi standard non polar	33892256
Nor-cocaine,1TMS,isomer #1	COC(=O)C1C(OC(=O)C2=CC=CC=C2)CC2CCC1N2[Si](C)(C)C	2282.0	Standard non polar	33892256
Nor-cocaine,1TMS,isomer #1	COC(=O)C1C(OC(=O)C2=CC=CC=C2)CC2CCC1N2[Si](C)(C)C	3193.0	Standard polar	33892256
Nor-cocaine,1TBDMS,isomer #1	COC(=O)C1C(OC(=O)C2=CC=CC=C2)CC2CCC1N2[Si](C)(C)C(C)(C)C	2485.7	Semi standard non polar	33892256
Nor-cocaine,1TBDMS,isomer #1	COC(=O)C1C(OC(=O)C2=CC=CC=C2)CC2CCC1N2[Si](C)(C)C(C)(C)C	2484.4	Standard non polar	33892256
Nor-cocaine,1TBDMS,isomer #1	COC(=O)C1C(OC(=O)C2=CC=CC=C2)CC2CCC1N2[Si](C)(C)C(C)(C)C	3300.7	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Nor-cocaine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-5910000000-c2136fbd697d57c69951	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Nor-cocaine 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 - Nor-cocaine 10V, Positive-QTOF	splash10-0a4l-0690000000-5cd0e067bc94a04da16a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Nor-cocaine 20V, Positive-QTOF	splash10-0a4i-0930000000-9c21418168233498ac4a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Nor-cocaine 40V, Positive-QTOF	splash10-0a4i-1910000000-8e318d46b4e919251daa	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Nor-cocaine 10V, Negative-QTOF	splash10-052r-2490000000-fcb93b2ed82e6ea3bf59	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Nor-cocaine 20V, Negative-QTOF	splash10-004i-7900000000-a6d19cde1594e866adc8	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Nor-cocaine 40V, Negative-QTOF	splash10-004i-9100000000-be58ee9c0ee645c3b476	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

519603

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

597722

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 Nor-cocaine (HMDB0249967)

MOL for HMDB0249967 (Nor-cocaine)

3D MOL for HMDB0249967 (Nor-cocaine)

3D SDF for HMDB0249967 (Nor-cocaine)

3D-SDF for HMDB0249967 (Nor-cocaine)

PDB for HMDB0249967 (Nor-cocaine)

3D PDB for HMDB0249967 (Nor-cocaine)

SMILES for HMDB0249967 (Nor-cocaine)

INCHI for HMDB0249967 (Nor-cocaine)

Structure for HMDB0249967 (Nor-cocaine)

3D Structure for HMDB0249967 (Nor-cocaine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra