Cinfenine

From WikiMD.com Medical Encyclopedia

A vasodilator drug


Cinfenine
[[File:
Chemical structure of Cinfenine
|frameless|220px|alt=|]]
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number 77-37-2
PubChem 68654
DrugBank
ChemSpider 61909
KEGG D07068


Cinfenine is a vasodilator drug that was developed for the treatment of angina pectoris. It functions by dilating the blood vessels, thereby improving blood flow and reducing the workload on the heart. This article provides an overview of its chemical properties, mechanism of action, and clinical applications.

Chemical Properties[edit | edit source]

Cinfenine is chemically classified as a ketone and belongs to the class of phenylpyrrolidines. Its systematic IUPAC name is 1-(2,3-dimethylphenyl)-2-(pyrrolidin-1-yl)ethanone. The molecular formula is C14H19NO, and it has a molecular weight of 217.31 g/mol.

The chemical structure of Cinfenine includes a pyrrolidine ring, which is a five-membered nitrogen-containing ring, and a dimethylphenyl group. This structure is crucial for its pharmacological activity as a vasodilator.

Mechanism of Action[edit | edit source]

Cinfenine acts primarily as a vasodilator. It works by relaxing the smooth muscles in the walls of blood vessels, leading to their dilation. This process decreases the vascular resistance and allows blood to flow more easily through the vessels. As a result, the heart does not have to work as hard to pump blood, which can alleviate symptoms of angina.

The exact molecular mechanism by which Cinfenine induces vasodilation is not fully understood, but it is believed to involve the modulation of calcium channels and possibly the adrenergic receptors.

Clinical Applications[edit | edit source]

Cinfenine was primarily used in the management of angina pectoris, a condition characterized by chest pain due to reduced blood flow to the heart muscle. By improving blood flow, Cinfenine helps to relieve the pain and discomfort associated with angina.

However, the use of Cinfenine has declined with the development of newer and more effective vasodilators and anti-anginal medications, such as beta blockers and calcium channel blockers.

Pharmacokinetics[edit | edit source]

The pharmacokinetic profile of Cinfenine includes its absorption, distribution, metabolism, and excretion. After administration, Cinfenine is absorbed into the bloodstream and distributed throughout the body. It is metabolized primarily in the liver and excreted via the kidneys.

Safety and Side Effects[edit | edit source]

As with many vasodilators, the use of Cinfenine can be associated with side effects such as headache, dizziness, and hypotension (low blood pressure). These effects are generally related to the vasodilatory action of the drug.

Related Pages[edit | edit source]

WikiMD
Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD