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Details

Stereochemistry RACEMIC
Molecular Formula C12H18ClN
Molecular Weight 211.731
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEFENOREX

SMILES

CC(CC1=CC=CC=C1)NCCCCl

InChI

InChIKey=XXVROGAVTTXONC-UHFFFAOYSA-N
InChI=1S/C12H18ClN/c1-11(14-9-5-8-13)10-12-6-3-2-4-7-12/h2-4,6-7,11,14H,5,8-10H2,1H3

HIDE SMILES / InChI

Molecular Formula C12H18ClN
Molecular Weight 211.731
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: description was created based on several sources, including, http://ec.europa.eu/health/documents/community-register/2000/200003093430/anx_3430_en.pdf

Mefenorex or (+/-)N-(3-chloropropyl)-1-methyl-2-phenylethylamine is an N-alkylated analogue of amphetamine. The therapeutic efficacy of mefenorex as an adjunctive support in the treatment of obesity for limited periods of time, as well as its ability to be well tolerated, has been amply demonstrated. Mefenorex is considered to be racemic mixture, no available data regarding enantiospecific pharmacological activity of the compound.

Originator

Curator's Comment: # Hoffmann-La Roche

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Pondinil

Approved Use

Adjunctive therapy to diet, in patients with obesity and a body mass index (BMI) of 30 kg/m2 or higher who have not responded to an appropriate weight-reducing regimen alone

Launch Date

1970
PubMed

PubMed

TitleDatePubMed
Toxicokinetics of amphetamines: metabolism and toxicokinetic data of designer drugs, amphetamine, methamphetamine, and their N-alkyl derivatives.
2002 Apr
Precursor medications as a source of methamphetamine and/or amphetamine positive drug testing results.
2002 May
Impaired cognition and attention in adults: pharmacological management strategies.
2007 Feb
Patents

Sample Use Guides

In Vivo Use Guide
40 mg/day
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:19:58 GMT 2023
Edited
by admin
on Fri Dec 15 17:19:58 GMT 2023
Record UNII
K98M4N387W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEFENOREX
INN   MI   WHO-DD  
INN  
Official Name English
MEFENOREX [MI]
Common Name English
N-(3-CHLOROPROPYL)-.ALPHA.-METHYLPHENETHYLAMINE
Systematic Name English
mefenorex [INN]
Common Name English
PHENETHYLAMINE, N-(3-CHLOROPROPYL)-.ALPHA.-METHYL-
Systematic Name English
Mefenorex [WHO-DD]
Common Name English
BENZENEETHANAMINE, N-(3-CHLOROPROPYL)-.ALPHA.-METHYL
Common Name English
Classification Tree Code System Code
WHO-ATC A08AA09
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
NCI_THESAURUS C29728
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
DEA NO. 1580
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
WHO-VATC QA08AA09
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
Code System Code Type Description
MERCK INDEX
m7140
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY Merck Index
ChEMBL
CHEMBL2110962
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
MESH
C000450
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
ECHA (EC/EINECS)
241-279-0
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID6057665
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
EVMPD
SUB08706MIG
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
CAS
17243-57-1
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
RXCUI
29444
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY RxNorm
DRUG BANK
DB13852
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
PUBCHEM
21777
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
INN
2494
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
NCI_THESAURUS
C83915
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
DRUG CENTRAL
1664
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
WIKIPEDIA
MEFENOREX
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
SMS_ID
100000081459
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
FDA UNII
K98M4N387W
Created by admin on Fri Dec 15 17:19:58 GMT 2023 , Edited by admin on Fri Dec 15 17:19:58 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY