Γ-Fagarine

From WikiMD.com - Food, Medicine & Wellness Encyclopedia

Chemical compound


Structural formula of γ-Fagarine

γ-Fagarine is a naturally occurring alkaloid found in various plant species, particularly within the Rutaceae family. It is known for its potential pharmacological properties and has been the subject of various studies due to its presence in traditional herbal medicine.

Chemical Structure and Properties[edit | edit source]

γ-Fagarine is classified as a quinoline alkaloid. Its chemical structure is characterized by a quinoline core, which is a bicyclic structure consisting of a benzene ring fused to a pyridine ring. This structure is common among alkaloids that exhibit a range of biological activities.

The molecular formula of γ-Fagarine is C12H9NO3, and it has a molecular weight of 215.21 g/mol. The presence of methoxy groups in its structure contributes to its chemical properties and potential biological activities.

Occurrence[edit | edit source]

γ-Fagarine is predominantly found in plants of the Rutaceae family, which includes species such as Fagara and Zanthoxylum. These plants are often used in traditional medicine systems across various cultures, particularly in Asia and Africa.

Biological Activity[edit | edit source]

Research into γ-Fagarine has revealed several potential biological activities. It has been studied for its antimicrobial, anti-inflammatory, and antioxidant properties. These activities make it a compound of interest for the development of new therapeutic agents.

Antimicrobial Properties[edit | edit source]

γ-Fagarine has shown activity against a range of bacteria and fungi, suggesting its potential use as a natural antimicrobial agent. This property is particularly valuable in the context of increasing antibiotic resistance.

Anti-inflammatory Effects[edit | edit source]

Studies have indicated that γ-Fagarine may help reduce inflammation, which is a common underlying factor in many chronic diseases. Its anti-inflammatory effects are thought to be mediated through the inhibition of pro-inflammatory mediators.

Antioxidant Activity[edit | edit source]

The antioxidant properties of γ-Fagarine contribute to its potential protective effects against oxidative stress, which is implicated in the pathogenesis of various diseases, including cardiovascular disease and cancer.

Potential Applications[edit | edit source]

Due to its diverse biological activities, γ-Fagarine is being explored for various applications in pharmaceutical and nutraceutical industries. Its natural origin and potential health benefits make it an attractive candidate for further research and development.

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