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fendiline

Structure via PubChem · Public domain (PubChem)

EntityQ999767· pop 6· linked from 327 articles

Fendiline is a nonselective calcium channel blocker and coronary vasodilator, originally developed for its anti-anginal and antiarrhythmic properties in the management of coronary heart disease.

Chemical data

Formula
C23H25N
Molecular weight
315.5 g/mol
IUPAC name
3,3-diphenyl-N-(1-phenylethyl)propan-1-amine

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule
Indications
cardiovascular disease

via ChEMBL · EBI

~1 min read

Encyclopedic overview

2 sections
Contents
  • References
  • Further reading

Fendiline is a nonselective calcium channel blocker and coronary vasodilator, originally developed for its anti-anginal and antiarrhythmic properties in the management of coronary heart disease.

By inhibiting the influx of calcium ions into cardiac and vascular smooth muscle cells, fendiline promotes vasodilation, particularly of the coronary arteries, thereby increasing blood flow to the heart muscle, alleviating ischemia, and reducing chest pain associated with angina. Although its clinical use has become limited due to the availability of alternative treatments and its relatively slow onset of action, fendiline remains notable for its long half-life, lack of tolerance development, and demonstrated efficacy in improving exercise tolerance and reducing the frequency of angina attacks in placebo-controlled trials.

Excerpted from Wikipedia’s “fendiline” article, available under the CC BY-SA 4.0 licence.

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