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

Details

Stereochemistry RACEMIC
Molecular Formula C12H16N2.ClH
Molecular Weight 224.73
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENPROPOREX HYDROCHLORIDE

SMILES

Cl.CC(CC1=CC=CC=C1)NCCC#N

InChI

InChIKey=ZBRZSJUFJUMKIM-UHFFFAOYSA-N
InChI=1S/C12H16N2.ClH/c1-11(14-9-5-8-13)10-12-6-3-2-4-7-12;/h2-4,6-7,11,14H,5,9-10H2,1H3;1H

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including: http://en.pharmacodia.com/web/drug/1_10952.html | http://www.ndrugs.com/?s=fenproporex%20hydrochloride&t=dosage | http://www.doctoralia.com.mx/medicamento/esbelcaps-53723

Fenproporex is a central and indirect-acting sympathomimetic. It was developed as an anorectic drug. Their anorectic effects are believed to be a result of adrenergic activation. Fenproporex has never been approved by the US Food and Drug Administration (FDA) for sale in the US due to lack of efficacy and safety data. There is a paucity of randomized, placebo-controlled trials on Fenproporex. These studies suggest that Fenproporex is modestly effective in promoting weight loss. Data from these studies are insufficient to determine the risk-benefit profile of Fenproporex. Abuse potential and amphetamine-like adverse effects are causes for concern. Adverse effect most frequently reported are: insomnia, anxiety, depression, irritability, dry mouth.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Esbelcaps

Approved Use

Anorexigenic. Assist in the treatment of obesity. An adjuvant to the establishment of a low-calorie diet.
PubMed

PubMed

TitleDatePubMed
Diabesity: are weight loss medications effective?
2005
Patents

Sample Use Guides

The initial dose is 10 mg/day. The dose might be increased up to 15 mg/day.
Route of Administration: Oral
In presence of 3 uM inhibitor quinidine and 50 uM Fenproporex the metabolite formation of the S(+)-enantiomer was significantly (P value 0.0145) inhibited.
Name Type Language
FENPROPOREX HYDROCHLORIDE
MART.   MI   WHO-DD  
Common Name English
Fenproporex hydrochloride [WHO-DD]
Common Name English
SOLVOLIP
Brand Name English
FENPROPOREX HCL
Common Name English
GACILIN
Brand Name English
(±)-3-(.ALPHA.-METHYLPHENETHYLAMINO)PROPIONITRILE HYDROCHLORIDE
Systematic Name English
(±)-N-2-CYANOETHYLAMPHETAMINE HYDROCHLORIDE
Systematic Name English
FENPROPOREX HYDROCHLORIDE [MI]
Common Name English
N-2-CYANOETHYLAMPHETAMINE HYDROCHLORIDE
Systematic Name English
FENPROPOREX HYDROCHLORIDE [MART.]
Common Name English
Code System Code Type Description
FDA UNII
09PE91J6V6
Created by admin on Fri Dec 15 18:30:15 GMT 2023 , Edited by admin on Fri Dec 15 18:30:15 GMT 2023
PRIMARY
CAS
16359-54-9
Created by admin on Fri Dec 15 18:30:14 GMT 2023 , Edited by admin on Fri Dec 15 18:30:14 GMT 2023
PRIMARY
EVMPD
SUB02126MIG
Created by admin on Fri Dec 15 18:30:15 GMT 2023 , Edited by admin on Fri Dec 15 18:30:15 GMT 2023
PRIMARY
SMS_ID
100000086985
Created by admin on Fri Dec 15 18:30:15 GMT 2023 , Edited by admin on Fri Dec 15 18:30:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID10936846
Created by admin on Fri Dec 15 18:30:15 GMT 2023 , Edited by admin on Fri Dec 15 18:30:15 GMT 2023
PRIMARY
MERCK INDEX
m5292
Created by admin on Fri Dec 15 18:30:15 GMT 2023 , Edited by admin on Fri Dec 15 18:30:15 GMT 2023
PRIMARY Merck Index
RXCUI
236528
Created by admin on Fri Dec 15 18:30:15 GMT 2023 , Edited by admin on Fri Dec 15 18:30:15 GMT 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
240-420-3
Created by admin on Fri Dec 15 18:30:15 GMT 2023 , Edited by admin on Fri Dec 15 18:30:15 GMT 2023
PRIMARY
PUBCHEM
161245
Created by admin on Fri Dec 15 18:30:15 GMT 2023 , Edited by admin on Fri Dec 15 18:30:15 GMT 2023
PRIMARY
CAS
18305-29-8
Created by admin on Fri Dec 15 18:30:14 GMT 2023 , Edited by admin on Fri Dec 15 18:30:14 GMT 2023
SUPERSEDED