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

2021-09-11 09:45:44 UTC

Update Date

2021-09-26 23:04:27 UTC

HMDB ID

HMDB0252083

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Ethylone

Description

Ethylone belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. Based on a literature review very few articles have been published on Ethylone. This compound has been identified in human blood as reported by (PMID: 31557052 ). Ethylone is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Ethylone 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

HMDB0252083
     RDKit          3D
Ethylone
 31 32  0  0  0  0  0  0  0  0999 V2000
   -4.5845    1.5622   -0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3948    0.7131   -0.5705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8495   -0.0110    0.5698 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6245   -0.7028    0.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7242   -2.1420    0.4029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489    0.0355    0.5468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7019    1.0560    1.3056 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.1918    0.2558 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023   -1.2667   -0.4961 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7479   -1.3817   -0.7510 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6805   -0.4513   -0.2812 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2491    0.6179    0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9120    0.7190    0.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3633    1.4049    0.8214 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3837    1.0589   -0.0918 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0717   -0.3108   -0.3837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0865    1.2933    0.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3143    2.6635   -0.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2689    1.4953   -1.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5487   -0.0232   -1.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5535    1.4133   -0.8693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6472    0.6138    1.3862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6461   -0.6026   -1.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1765   -2.5053    1.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4818   -2.8234   -0.4698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8144   -2.3894    0.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7002   -2.0040   -0.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1352   -2.2056   -1.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828    1.5847    1.3068 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2893    1.7137   -0.9885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4003    1.0663    0.3555 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 13  8  1  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  5 26  1  0
  9 27  1  0
 10 28  1  0
 13 29  1  0
 15 30  1  0
 15 31  1  0
M  END


  Mrv1652306031609462D          

 16 17  0  0  0  0            999 V2000
   -3.5724    1.2375    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
   -2.8579    0.8250    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
    0.7145   -0.4125    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
    2.6985    0.4125    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
    0.0000    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
    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
   -2.1434    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2136   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2136    1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  5  4  2  0  0  0  0
  8  2  1  0  0  0  0
  9  4  1  0  0  0  0
  9  6  2  0  0  0  0
 10  5  1  0  0  0  0
 11  6  1  0  0  0  0
 11 10  2  0  0  0  0
 12  8  1  0  0  0  0
 12  9  1  0  0  0  0
 13  3  1  0  0  0  0
 13  8  1  0  0  0  0
 14 12  2  0  0  0  0
 15  7  1  0  0  0  0
 15 10  1  0  0  0  0
 16  7  1  0  0  0  0
 16 11  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0252083

> <DATABASE_NAME>
hmdb

> <SMILES>
CCNC(C)C(=O)C1=CC2=C(OCO2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C12H15NO3/c1-3-13-8(2)12(14)9-4-5-10-11(6-9)16-7-15-10/h4-6,8,13H,3,7H2,1-2H3

> <INCHI_KEY>
MJEMIOXXNCZZFK-UHFFFAOYSA-N

> <FORMULA>
C12H15NO3

> <MOLECULAR_WEIGHT>
221.256

> <EXACT_MASS>
221.105193347

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
23.44067650375627

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(2H-1,3-benzodioxol-5-yl)-2-(ethylamino)propan-1-one

> <ALOGPS_LOGP>
1.36

> <JCHEM_LOGP>
1.5881495503333334

> <ALOGPS_LOGS>
-1.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.490685994984823

> <JCHEM_PKA_STRONGEST_BASIC>
8.042975758873624

> <JCHEM_POLAR_SURFACE_AREA>
47.56

> <JCHEM_REFRACTIVITY>
59.60450000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.44e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ethylone

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0252083
     RDKit          3D
Ethylone
 31 32  0  0  0  0  0  0  0  0999 V2000
   -4.5845    1.5622   -0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3948    0.7131   -0.5705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8495   -0.0110    0.5698 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6245   -0.7028    0.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7242   -2.1420    0.4029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489    0.0355    0.5468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7019    1.0560    1.3056 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.1918    0.2558 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023   -1.2667   -0.4961 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7479   -1.3817   -0.7510 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6805   -0.4513   -0.2812 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2491    0.6179    0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9120    0.7190    0.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3633    1.4049    0.8214 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3837    1.0589   -0.0918 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0717   -0.3108   -0.3837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0865    1.2933    0.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3143    2.6635   -0.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2689    1.4953   -1.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5487   -0.0232   -1.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5535    1.4133   -0.8693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6472    0.6138    1.3862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6461   -0.6026   -1.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1765   -2.5053    1.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4818   -2.8234   -0.4698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8144   -2.3894    0.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7002   -2.0040   -0.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1352   -2.2056   -1.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828    1.5847    1.3068 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2893    1.7137   -0.9885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4003    1.0663    0.3555 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 13  8  1  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  5 26  1  0
  9 27  1  0
 10 28  1  0
 13 29  1  0
 15 30  1  0
 15 31  1  0
M  END

HEADER    PROTEIN                                 03-JUN-16   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-JUN-16         0                                  
HETATM    1  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.037   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667   1.540   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       2.667   0.000   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      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -4.001   2.310   0.000  0.00  0.00           N+0
HETATM   14  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       4.132  -0.476   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       4.132   2.016   0.000  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2    8                                                            
CONECT    3    1   13                                                       
CONECT    4    5    9                                                       
CONECT    5    4   10                                                       
CONECT    6    9   11                                                       
CONECT    7   15   16                                                       
CONECT    8    2   12   13                                                  
CONECT    9    4    6   12                                                  
CONECT   10    5   11   15                                                  
CONECT   11    6   10   16                                                  
CONECT   12    8    9   14                                                  
CONECT   13    3    8                                                       
CONECT   14   12                                                            
CONECT   15    7   10                                                       
CONECT   16    7   11                                                       
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

COMPND    HMDB0252083
HETATM    1  C1  UNL     1      -4.585   1.562  -0.261  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.395   0.713  -0.570  1.00  0.00           C  
HETATM    3  N1  UNL     1      -2.850  -0.011   0.570  1.00  0.00           N  
HETATM    4  C3  UNL     1      -1.624  -0.703   0.112  1.00  0.00           C  
HETATM    5  C4  UNL     1      -1.724  -2.142   0.403  1.00  0.00           C  
HETATM    6  C5  UNL     1      -0.449   0.036   0.547  1.00  0.00           C  
HETATM    7  O1  UNL     1      -0.702   1.056   1.306  1.00  0.00           O  
HETATM    8  C6  UNL     1       0.948  -0.192   0.256  1.00  0.00           C  
HETATM    9  C7  UNL     1       1.402  -1.267  -0.496  1.00  0.00           C  
HETATM   10  C8  UNL     1       2.748  -1.382  -0.751  1.00  0.00           C  
HETATM   11  C9  UNL     1       3.680  -0.451  -0.281  1.00  0.00           C  
HETATM   12  C10 UNL     1       3.249   0.618   0.466  1.00  0.00           C  
HETATM   13  C11 UNL     1       1.912   0.719   0.713  1.00  0.00           C  
HETATM   14  O2  UNL     1       4.363   1.405   0.821  1.00  0.00           O  
HETATM   15  C12 UNL     1       5.384   1.059  -0.092  1.00  0.00           C  
HETATM   16  O3  UNL     1       5.072  -0.311  -0.384  1.00  0.00           O  
HETATM   17  H1  UNL     1      -5.087   1.293   0.670  1.00  0.00           H  
HETATM   18  H2  UNL     1      -4.314   2.663  -0.218  1.00  0.00           H  
HETATM   19  H3  UNL     1      -5.269   1.495  -1.154  1.00  0.00           H  
HETATM   20  H4  UNL     1      -3.549  -0.023  -1.376  1.00  0.00           H  
HETATM   21  H5  UNL     1      -2.554   1.413  -0.869  1.00  0.00           H  
HETATM   22  H6  UNL     1      -2.647   0.614   1.386  1.00  0.00           H  
HETATM   23  H7  UNL     1      -1.646  -0.603  -1.019  1.00  0.00           H  
HETATM   24  H8  UNL     1      -1.177  -2.505   1.308  1.00  0.00           H  
HETATM   25  H9  UNL     1      -1.482  -2.823  -0.470  1.00  0.00           H  
HETATM   26  H10 UNL     1      -2.814  -2.389   0.601  1.00  0.00           H  
HETATM   27  H11 UNL     1       0.700  -2.004  -0.886  1.00  0.00           H  
HETATM   28  H12 UNL     1       3.135  -2.206  -1.326  1.00  0.00           H  
HETATM   29  H13 UNL     1       1.583   1.585   1.307  1.00  0.00           H  
HETATM   30  H14 UNL     1       5.289   1.714  -0.989  1.00  0.00           H  
HETATM   31  H15 UNL     1       6.400   1.066   0.356  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3   20   21
CONECT    3    4   22
CONECT    4    5    6   23
CONECT    5   24   25   26
CONECT    6    7    7    8
CONECT    8    9    9   13
CONECT    9   10   27
CONECT   10   11   11   28
CONECT   11   12   16
CONECT   12   13   13   14
CONECT   13   29
CONECT   14   15
CONECT   15   16   30   31
END

HMDB0252083
     RDKit          3D
Ethylone
 31 32  0  0  0  0  0  0  0  0999 V2000
   -4.5845    1.5622   -0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3948    0.7131   -0.5705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8495   -0.0110    0.5698 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6245   -0.7028    0.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7242   -2.1420    0.4029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489    0.0355    0.5468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7019    1.0560    1.3056 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.1918    0.2558 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023   -1.2667   -0.4961 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7479   -1.3817   -0.7510 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6805   -0.4513   -0.2812 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2491    0.6179    0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9120    0.7190    0.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3633    1.4049    0.8214 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3837    1.0589   -0.0918 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0717   -0.3108   -0.3837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0865    1.2933    0.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3143    2.6635   -0.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2689    1.4953   -1.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5487   -0.0232   -1.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5535    1.4133   -0.8693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6472    0.6138    1.3862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6461   -0.6026   -1.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1765   -2.5053    1.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4818   -2.8234   -0.4698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8144   -2.3894    0.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7002   -2.0040   -0.8859 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1352   -2.2056   -1.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828    1.5847    1.3068 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2893    1.7137   -0.9885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4003    1.0663    0.3555 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 13  8  1  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  5 26  1  0
  9 27  1  0
 10 28  1  0
 13 29  1  0
 15 30  1  0
 15 31  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
2-Ethylammonio-1-(3,4-methylenedioxyphenyl)propane-1-one chloride	MeSH
2-Ethylamino-1-(3,4-methylenedioxyphenyl)propan-1-one	MeSH
BK-MDEA	MeSH

Chemical Formula

C₁₂H₁₅NO₃

Average Molecular Weight

221.256

Monoisotopic Molecular Weight

221.105193347

IUPAC Name

1-(2H-1,3-benzodioxol-5-yl)-2-(ethylamino)propan-1-one

Traditional Name

ethylone

CAS Registry Number

Not Available

SMILES

CCNC(C)C(=O)C1=CC2=C(OCO2)C=C1

InChI Identifier

InChI=1S/C12H15NO3/c1-3-13-8(2)12(14)9-4-5-10-11(6-9)16-7-15-10/h4-6,8,13H,3,7H2,1-2H3

InChI Key

MJEMIOXXNCZZFK-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxoles

Sub Class

Not Available

Direct Parent

Benzodioxoles

Alternative Parents

Substituents

Benzodioxole
Aryl ketone
Aryl alkyl ketone
Benzenoid
Alpha-aminoketone
Ketone
Acetal
Secondary aliphatic amine
Secondary amine
Oxacycle
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic nitrogen compound
Organic oxygen compound
Amine
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.36	ALOGPS
logP	1.59	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	18.49	ChemAxon
pKa (Strongest Basic)	8.04	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	47.56 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	59.6 m³·mol⁻¹	ChemAxon
Polarizability	23.44 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	152.536	30932474
DeepCCS	[M-H]-	150.178	30932474
DeepCCS	[M-2H]-	183.153	30932474
DeepCCS	[M+Na]+	158.629	30932474
AllCCS	[M+H]+	149.8	32859911
AllCCS	[M+H-H2O]+	145.9	32859911
AllCCS	[M+NH4]+	153.6	32859911
AllCCS	[M+Na]+	154.6	32859911
AllCCS	[M-H]-	153.9	32859911
AllCCS	[M+Na-2H]-	154.1	32859911
AllCCS	[M+HCOO]-	154.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Ethylone	CCNC(C)C(=O)C1=CC2=C(OCO2)C=C1	2664.1	Standard polar	33892256
Ethylone	CCNC(C)C(=O)C1=CC2=C(OCO2)C=C1	1858.5	Standard non polar	33892256
Ethylone	CCNC(C)C(=O)C1=CC2=C(OCO2)C=C1	1758.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Ethylone,1TMS,isomer #1	CCN(C(C)C(=O)C1=CC=C2OCOC2=C1)[Si](C)(C)C	1883.0	Semi standard non polar	33892256
Ethylone,1TMS,isomer #1	CCN(C(C)C(=O)C1=CC=C2OCOC2=C1)[Si](C)(C)C	1954.8	Standard non polar	33892256
Ethylone,1TMS,isomer #1	CCN(C(C)C(=O)C1=CC=C2OCOC2=C1)[Si](C)(C)C	2624.6	Standard polar	33892256
Ethylone,1TBDMS,isomer #1	CCN(C(C)C(=O)C1=CC=C2OCOC2=C1)[Si](C)(C)C(C)(C)C	2133.1	Semi standard non polar	33892256
Ethylone,1TBDMS,isomer #1	CCN(C(C)C(=O)C1=CC=C2OCOC2=C1)[Si](C)(C)C(C)(C)C	2172.0	Standard non polar	33892256
Ethylone,1TBDMS,isomer #1	CCN(C(C)C(=O)C1=CC=C2OCOC2=C1)[Si](C)(C)C(C)(C)C	2743.2	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Ethylone GC-MS (Non-derivatized) - 70eV, Positive	splash10-00dj-9510000000-7e9e40b131effa015b52	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Ethylone 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 - Ethylone 10V, Positive-QTOF	splash10-00di-1090000000-30aba7b1105b97c5103c	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 20V, Positive-QTOF	splash10-00di-5690000000-d0f7309d243cd0e6ab78	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 40V, Positive-QTOF	splash10-00ba-9400000000-8acf4950fd91e2e48d5f	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 10V, Negative-QTOF	splash10-00di-0090000000-dc4e9a10d5adbd1e0ebd	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 20V, Negative-QTOF	splash10-00di-4490000000-c13c58c1394fbc8a35f6	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 40V, Negative-QTOF	splash10-006x-9610000000-6245dd5474141a1e243d	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 10V, Positive-QTOF	splash10-00di-0390000000-0d3c27ecfed69446c5e8	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 20V, Positive-QTOF	splash10-0fb9-0940000000-ce9d0c07f6e47892f498	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 40V, Positive-QTOF	splash10-05fs-2900000000-e4b88c4bb86511f1fc0c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 10V, Negative-QTOF	splash10-00di-0090000000-f619947f25b2f196c975	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 20V, Negative-QTOF	splash10-00fr-1970000000-2b424a3b0d04cf0a5ca7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethylone 40V, Negative-QTOF	splash10-01ot-3900000000-5f73dcb78b8c096794c0	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	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

21106271

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Ethylone

METLIN ID

Not Available

PubChem Compound

57252245

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 Ethylone (HMDB0252083)

MOL for HMDB0252083 (Ethylone)

3D MOL for HMDB0252083 (Ethylone)

3D SDF for HMDB0252083 (Ethylone)

3D-SDF for HMDB0252083 (Ethylone)

PDB for HMDB0252083 (Ethylone)

3D PDB for HMDB0252083 (Ethylone)

SMILES for HMDB0252083 (Ethylone)

INCHI for HMDB0252083 (Ethylone)

Structure for HMDB0252083 (Ethylone)

3D Structure for HMDB0252083 (Ethylone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra