Naringenin
Naringenin[edit | edit source]
Naringenin is a flavanone, a type of flavonoid found in various citrus fruits. It is a colorless, water-insoluble solid that is considered to have various health benefits due to its antioxidant properties.
Chemical Properties[edit | edit source]
Naringenin has the chemical formula C15H12O5. It is a derivative of flavanone and is structurally related to other flavonoids such as hesperetin and quercetin. The compound is characterized by its three-ring structure, which includes a phenyl group and a chroman ring.
Sources[edit | edit source]
Naringenin is predominantly found in citrus fruits such as grapefruit, oranges, and lemons. It is also present in smaller amounts in other fruits like tomatoes and figs. The concentration of naringenin can vary depending on the type of fruit and its ripeness.
Biological Effects[edit | edit source]
Naringenin is known for its potential antioxidant, anti-inflammatory, and anticancer properties. It has been studied for its ability to modulate enzyme activity, particularly in the liver, where it can influence the metabolism of lipids and carbohydrates.
Antioxidant Activity[edit | edit source]
As an antioxidant, naringenin helps to neutralize free radicals in the body, which can prevent cellular damage and reduce the risk of chronic diseases such as cardiovascular disease and cancer.
Anti-inflammatory Effects[edit | edit source]
Naringenin has been shown to reduce inflammation by inhibiting the production of pro-inflammatory cytokines. This makes it a compound of interest in the treatment of inflammatory diseases such as arthritis and asthma.
Anticancer Potential[edit | edit source]
Research suggests that naringenin may have anticancer properties by inducing apoptosis in cancer cells and inhibiting their proliferation. It has been studied in various types of cancer, including breast cancer, prostate cancer, and colon cancer.
Metabolism[edit | edit source]
Naringenin is metabolized in the human body primarily in the liver. It undergoes phase II metabolism, where it is conjugated with glucuronic acid or sulfate to form more water-soluble metabolites that can be excreted in the urine.
Potential Health Benefits[edit | edit source]
Due to its various biological activities, naringenin is being investigated for its potential health benefits, including its role in improving cardiovascular health, managing diabetes, and supporting weight loss.
Related Pages[edit | edit source]
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 |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
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