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Showing metabocard for Flephedrone (HMDB0252298)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-11 10:10:33 UTC
Update Date2021-09-26 23:04:47 UTC
HMDB IDHMDB0252298
Secondary Accession NumbersNone
Metabolite Identification
Common NameFlephedrone
Description1-(4-fluorophenyl)-2-(methylamino)propan-1-one belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Based on a literature review very few articles have been published on 1-(4-fluorophenyl)-2-(methylamino)propan-1-one. This compound has been identified in human blood as reported by (PMID: 31557052 ). Flephedrone is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Flephedrone 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
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MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0252298 (Flephedrone)


  Mrv1652306031609462D          

 13 13  0  0  0  0            999 V2000
   -0.7145   -1.2375    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   -0.0000    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
    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
   -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
    0.7145    1.2375    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 F   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
  7  1  1  0  0  0  0
  8  3  2  0  0  0  0
  8  4  1  0  0  0  0
  9  5  2  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12  2  1  0  0  0  0
 12  7  1  0  0  0  0
 13 10  2  0  0  0  0
M  END
Download

3D MOL for HMDB0252298 (Flephedrone)

HMDB0252298
     RDKit          3D
Flephedrone
 25 25  0  0  0  0  0  0  0  0999 V2000
   -3.2071   -0.8363   -0.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9117   -0.3536   -0.5423 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3342    0.7910    0.0521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7403    2.1536   -0.2741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1345    0.5868    0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1617    0.9183    2.0910 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1681    0.0278    0.3754 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1889    0.6664   -0.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4315    0.0250   -0.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6217   -1.2823   -0.1435 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8157   -1.9586   -0.3643 F   0  0  0  0  0  0  0  0  0  0  0  0
    2.5788   -1.9801    0.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3861   -1.3360    0.7000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9773   -0.9230   -0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6256   -0.3720    0.7710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0690   -1.9469    0.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0186   -0.1413   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1194    0.7443    1.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0039    2.6997   -0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7597    2.2819   -0.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6840    2.7713    0.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0943    1.7262   -0.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2294    0.5939   -0.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6984   -3.0244    0.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5342   -1.8318    1.1386 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
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13  7  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  4 19  1  0
  4 20  1  0
  4 21  1  0
  8 22  1  0
  9 23  1  0
 12 24  1  0
 13 25  1  0
M  END
Download

3D SDF for HMDB0252298 (Flephedrone)


  Mrv1652306031609462D          

 13 13  0  0  0  0            999 V2000
   -0.7145   -1.2375    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   -0.0000    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
    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
   -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
    0.7145    1.2375    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 F   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
  7  1  1  0  0  0  0
  8  3  2  0  0  0  0
  8  4  1  0  0  0  0
  9  5  2  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12  2  1  0  0  0  0
 12  7  1  0  0  0  0
 13 10  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0252298

> <DATABASE_NAME>
hmdb

> <SMILES>
CNC(C)C(=O)C1=CC=C(F)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C10H12FNO/c1-7(12-2)10(13)8-3-5-9(11)6-4-8/h3-7,12H,1-2H3

> <INCHI_KEY>
MWKQPIROPJSFRI-UHFFFAOYSA-N

> <FORMULA>
C10H12FNO

> <MOLECULAR_WEIGHT>
181.21

> <EXACT_MASS>
181.090292173

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
25

> <JCHEM_AVERAGE_POLARIZABILITY>
18.531711788966778

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(4-fluorophenyl)-2-(methylamino)propan-1-one

> <ALOGPS_LOGP>
1.15

> <JCHEM_LOGP>
1.7508100643333337

> <ALOGPS_LOGS>
-2.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.56700595345566

> <JCHEM_PKA_STRONGEST_BASIC>
7.9778632417242115

> <JCHEM_POLAR_SURFACE_AREA>
29.1

> <JCHEM_REFRACTIVITY>
49.305400000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.20e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
flephedrone

> <JCHEM_VEBER_RULE>
1

$$$$
Download

3D-SDF for HMDB0252298 (Flephedrone)

HMDB0252298
     RDKit          3D
Flephedrone
 25 25  0  0  0  0  0  0  0  0999 V2000
   -3.2071   -0.8363   -0.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9117   -0.3536   -0.5423 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3342    0.7910    0.0521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7403    2.1536   -0.2741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1345    0.5868    0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1617    0.9183    2.0910 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1681    0.0278    0.3754 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1889    0.6664   -0.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4315    0.0250   -0.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6217   -1.2823   -0.1435 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8157   -1.9586   -0.3643 F   0  0  0  0  0  0  0  0  0  0  0  0
    2.5788   -1.9801    0.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3861   -1.3360    0.7000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9773   -0.9230   -0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6256   -0.3720    0.7710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0690   -1.9469    0.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0186   -0.1413   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1194    0.7443    1.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0039    2.6997   -0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7597    2.2819   -0.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6840    2.7713    0.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0943    1.7262   -0.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2294    0.5939   -0.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6984   -3.0244    0.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5342   -1.8318    1.1386 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
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13  7  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  4 19  1  0
  4 20  1  0
  4 21  1  0
  8 22  1  0
  9 23  1  0
 12 24  1  0
 13 25  1  0
M  END
Download

PDB for HMDB0252298 (Flephedrone)

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      -1.334  -2.310   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  -0.000   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       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  F   UNK     0       1.334   3.850   0.000  0.00  0.00           F+0
HETATM   12  N   UNK     0      -0.000  -4.620   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    7                                                            
CONECT    2   12                                                            
CONECT    3    5    8                                                       
CONECT    4    6    8                                                       
CONECT    5    3    9                                                       
CONECT    6    4    9                                                       
CONECT    7    1   10   12                                                  
CONECT    8    3    4   10                                                  
CONECT    9    5    6   11                                                  
CONECT   10    7    8   13                                                  
CONECT   11    9                                                            
CONECT   12    2    7                                                       
CONECT   13   10                                                            
MASTER        0    0    0    0    0    0    0    0   13    0   26    0
END
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3D PDB for HMDB0252298 (Flephedrone)

COMPND    HMDB0252298
HETATM    1  C1  UNL     1      -3.207  -0.836  -0.120  1.00  0.00           C  
HETATM    2  N1  UNL     1      -1.912  -0.354  -0.542  1.00  0.00           N  
HETATM    3  C2  UNL     1      -1.334   0.791   0.052  1.00  0.00           C  
HETATM    4  C3  UNL     1      -1.740   2.154  -0.274  1.00  0.00           C  
HETATM    5  C4  UNL     1      -0.135   0.587   0.815  1.00  0.00           C  
HETATM    6  O1  UNL     1      -0.162   0.918   2.091  1.00  0.00           O  
HETATM    7  C5  UNL     1       1.168   0.028   0.375  1.00  0.00           C  
HETATM    8  C6  UNL     1       2.189   0.666  -0.198  1.00  0.00           C  
HETATM    9  C7  UNL     1       3.432   0.025  -0.467  1.00  0.00           C  
HETATM   10  C8  UNL     1       3.622  -1.282  -0.143  1.00  0.00           C  
HETATM   11  F1  UNL     1       4.816  -1.959  -0.364  1.00  0.00           F  
HETATM   12  C9  UNL     1       2.579  -1.980   0.446  1.00  0.00           C  
HETATM   13  C10 UNL     1       1.386  -1.336   0.700  1.00  0.00           C  
HETATM   14  H1  UNL     1      -3.977  -0.923  -0.941  1.00  0.00           H  
HETATM   15  H2  UNL     1      -3.626  -0.372   0.771  1.00  0.00           H  
HETATM   16  H3  UNL     1      -3.069  -1.947   0.205  1.00  0.00           H  
HETATM   17  H4  UNL     1      -2.019  -0.141  -1.621  1.00  0.00           H  
HETATM   18  H5  UNL     1      -2.119   0.744   1.103  1.00  0.00           H  
HETATM   19  H6  UNL     1      -1.004   2.700  -0.931  1.00  0.00           H  
HETATM   20  H7  UNL     1      -2.760   2.282  -0.723  1.00  0.00           H  
HETATM   21  H8  UNL     1      -1.684   2.771   0.692  1.00  0.00           H  
HETATM   22  H9  UNL     1       2.094   1.726  -0.464  1.00  0.00           H  
HETATM   23  H10 UNL     1       4.229   0.594  -0.916  1.00  0.00           H  
HETATM   24  H11 UNL     1       2.698  -3.024   0.698  1.00  0.00           H  
HETATM   25  H12 UNL     1       0.534  -1.832   1.139  1.00  0.00           H  
CONECT    1    2   14   15   16
CONECT    2    3   17
CONECT    3    4    5   18
CONECT    4   19   20   21
CONECT    5    6    6    7
CONECT    7    8    8   13
CONECT    8    9   22
CONECT    9   10   10   23
CONECT   10   11   12
CONECT   12   13   13   24
CONECT   13   25
END
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SMILES for HMDB0252298 (Flephedrone)

CNC(C)C(=O)C1=CC=C(F)C=C1
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INCHI for HMDB0252298 (Flephedrone)

InChI=1S/C10H12FNO/c1-7(12-2)10(13)8-3-5-9(11)6-4-8/h3-7,12H,1-2H3
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View in JSmolView Stereo Labels
Synonyms
ValueSource
4-FluoromethcathinoneMeSH
Chemical FormulaC10H12FNO
Average Molecular Weight181.21
Monoisotopic Molecular Weight181.090292173
IUPAC Name1-(4-fluorophenyl)-2-(methylamino)propan-1-one
Traditional Nameflephedrone
CAS Registry NumberNot Available
SMILES
CNC(C)C(=O)C1=CC=C(F)C=C1
InChI Identifier
InChI=1S/C10H12FNO/c1-7(12-2)10(13)8-3-5-9(11)6-4-8/h3-7,12H,1-2H3
InChI KeyMWKQPIROPJSFRI-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbonyl compounds
Direct ParentAlkyl-phenylketones
Alternative Parents
Substituents
  • Alkyl-phenylketone
  • Phenylpropane
  • Benzoyl
  • Aryl alkyl ketone
  • Fluorobenzene
  • Halobenzene
  • Aryl fluoride
  • Aryl halide
  • Monocyclic benzene moiety
  • Benzenoid
  • Alpha-aminoketone
  • Secondary aliphatic amine
  • Secondary amine
  • Organofluoride
  • Organohalogen compound
  • Organic oxide
  • Organopnictogen compound
  • Organic nitrogen compound
  • Amine
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
logP1.15ALOGPS
logP1.75ChemAxon
logS-2.2ALOGPS
pKa (Strongest Acidic)18.57ChemAxon
pKa (Strongest Basic)7.98ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area29.1 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity49.31 m³·mol⁻¹ChemAxon
Polarizability18.53 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+142.30730932474
DeepCCS[M-H]-139.46730932474
DeepCCS[M-2H]-175.76530932474
DeepCCS[M+Na]+151.30330932474
AllCCS[M+H]+140.032859911
AllCCS[M+H-H2O]+135.732859911
AllCCS[M+NH4]+144.032859911
AllCCS[M+Na]+145.132859911
AllCCS[M-H]-140.432859911
AllCCS[M+Na-2H]-141.332859911
AllCCS[M+HCOO]-142.432859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Predicted by Siyang on May 30, 202210.1728 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20223.01 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid1134.1 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid307.9 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid112.1 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid179.1 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid81.9 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid281.5 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid341.8 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)240.3 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid831.1 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid313.4 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid917.7 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid222.6 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid261.7 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate360.0 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA266.8 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water70.1 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
FlephedroneCNC(C)C(=O)C1=CC=C(F)C=C11957.5Standard polar33892256
FlephedroneCNC(C)C(=O)C1=CC=C(F)C=C11315.1Standard non polar33892256
FlephedroneCNC(C)C(=O)C1=CC=C(F)C=C11340.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Flephedrone,1TMS,isomer #1CC(C(=O)C1=CC=C(F)C=C1)N(C)[Si](C)(C)C1504.4Semi standard non polar33892256
Flephedrone,1TMS,isomer #1CC(C(=O)C1=CC=C(F)C=C1)N(C)[Si](C)(C)C1563.2Standard non polar33892256
Flephedrone,1TMS,isomer #1CC(C(=O)C1=CC=C(F)C=C1)N(C)[Si](C)(C)C1714.0Standard polar33892256
Flephedrone,1TBDMS,isomer #1CC(C(=O)C1=CC=C(F)C=C1)N(C)[Si](C)(C)C(C)(C)C1750.7Semi standard non polar33892256
Flephedrone,1TBDMS,isomer #1CC(C(=O)C1=CC=C(F)C=C1)N(C)[Si](C)(C)C(C)(C)C1767.1Standard non polar33892256
Flephedrone,1TBDMS,isomer #1CC(C(=O)C1=CC=C(F)C=C1)N(C)[Si](C)(C)C(C)(C)C1870.6Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Flephedrone GC-MS (Non-derivatized) - 70eV, Positivesplash10-0ab9-9600000000-2f141ace47d6c53fd8692021-09-24Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Flephedrone GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 10V, Positive-QTOFsplash10-001i-0900000000-9355443d276175f9c21a2019-02-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 20V, Positive-QTOFsplash10-001i-2900000000-a1be1cef3f059a7a23892019-02-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 40V, Positive-QTOFsplash10-0abc-9400000000-519298fb58115bd66ead2019-02-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 10V, Negative-QTOFsplash10-001i-0900000000-0c3295bee2df6c9f222e2019-02-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 20V, Negative-QTOFsplash10-001i-2900000000-df1d2cfe84f3d1b1c1182019-02-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 40V, Negative-QTOFsplash10-0002-8900000000-fda9a660fbafc7b59e5a2019-02-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 10V, Positive-QTOFsplash10-03di-0900000000-f52d1706b4e8491ff5572021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 20V, Positive-QTOFsplash10-03di-0900000000-45a72d0750d64033d72a2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 40V, Positive-QTOFsplash10-0002-2900000000-8370a4d1093ca9add8d42021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 10V, Negative-QTOFsplash10-001i-0900000000-075175a83329262e531e2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 20V, Negative-QTOFsplash10-000t-2900000000-d010281b85c3e31e15102021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Flephedrone 40V, Negative-QTOFsplash10-0002-9800000000-7bc93ac1294af9eea0f12021-10-12Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID21477355
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound49853406
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. 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 ]