U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C12H16F3N
Molecular Weight 231.2573
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOFENFLURAMINE

SMILES

CCN[C@H](C)CC1=CC(=CC=C1)C(F)(F)F

InChI

InChIKey=DBGIVFWFUFKIQN-SECBINFHSA-N
InChI=1S/C12H16F3N/c1-3-16-9(2)7-10-5-4-6-11(8-10)12(13,14)15/h4-6,8-9,16H,3,7H2,1-2H3/t9-/m1/s1

HIDE SMILES / InChI
LEVOFENFLURAMINE is a levorotatory enantiomer of fenfluramine, a substituted amphetamine which was formerly used to treat obesity. LEVOFENFLURAMINE has dopamine-antagonistic properties and, at high doses, increases dopamine concentrations in rat striatal dialysates. It is essentially inactive to reduce food intake in human subjects.

Approval Year

PubMed

PubMed

TitleDatePubMed
Neuroleptic-like effects of the l-isomer of fenfluramine on striatal dopamine release in freely moving rats.
1987 Jul 15
The effects of D- and L-fenfluramine (and their interactions with D-amphetamine) on psychomotor function and mood.
1996 Jun
Medicine as a corporate enterprise, patient welfare centered profession, or patient welfare centered professional enterprise?
2005 Nov
Off-label promotion, on-target sales.
2008 Oct 28
Name Type Language
LEVOFENFLURAMINE
INN  
INN  
Official Name English
R)-(-)-FENFLURAMINE
Common Name English
(-)-FENFLURAMINE
Common Name English
L-FENFLURAMINE
Common Name English
BENZENEETHANAMINE, N-ETHYL-.ALPHA.-METHYL-3-(TRIFLUOROMETHYL)-, (.ALPHA.R)-
Common Name English
BENZENEETHANAMINE, N-ETHYL-.ALPHA.-METHYL-3-(TRIFLUOROMETHYL)-, (R)-
Systematic Name English
J50.055K
Code English
levofenfluramine [INN]
Common Name English
(-)-(R)-N-ETHYL-.ALPHA.-METHYL-M-(TRIFLUOROMETHYL)PHENETHYLAMINE
Systematic Name English
FENFLURAMINE L-FORM
MI  
Common Name English
FENFLURAMINE L-FORM [MI]
Common Name English
FENFLURAMINE, L-
Common Name English
Classification Tree Code System Code
DEA NO. 1670
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
Code System Code Type Description
CAS
3616-77-1
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
SUPERSEDED
CAS
37577-24-5
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID60191009
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
NCI_THESAURUS
C175112
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
CHEBI
521051
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
EVMPD
SUB08470MIG
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
WIKIPEDIA
Levofenfluramine
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
INN
6132
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
FDA UNII
953A94Y45B
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
PUBCHEM
65801
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
SMS_ID
100000082295
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY
MERCK INDEX
m5274
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY Merck Index
ChEMBL
CHEMBL438145
Created by admin on Fri Dec 15 18:51:58 GMT 2023 , Edited by admin on Fri Dec 15 18:51:58 GMT 2023
PRIMARY