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
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
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/27253901Curator'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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27253901
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.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL3356 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15294457 |
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Target ID: P20813 Gene ID: 1555.0 Gene Symbol: CYP2B6 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/15294457 |
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Target ID: CHEMBL2890 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15294457 |
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Target ID: CHEMBL340 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15294457 |
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Target ID: CHEMBL3199 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26247155 |
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Target ID: Sodium-Potassium-Exchanging ATPase (Rat) Sources: https://www.ncbi.nlm.nih.gov/pubmed/24217638 |
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Target ID: CHEMBL2331074 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Esbelcaps Approved UseAnorexigenic. Assist in the treatment of obesity. An adjuvant to the establishment of a low-calorie diet. |
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 Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15294457
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.
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09PE91J6V6
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16359-54-9
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SUB02126MIG
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100000086985
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DTXSID10936846
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m5292
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236528
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240-420-3
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161245
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18305-29-8
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SUPERSEDED |
ACTIVE MOIETY
SUBSTANCE RECORD