Ricinine
Ricinine[edit | edit source]
Ricinine is a naturally occurring toxic alkaloid found in the seeds of the castor oil plant, scientifically known as Ricinus communis. It is classified as a phytotoxin, which means it is toxic to plants, animals, and humans. Ricinine has gained attention due to its potential use as a poison and its role in forensic toxicology.
Chemical Properties[edit | edit source]
Ricinine is a white, crystalline substance with a bitter taste. It is soluble in water, alcohol, and ether. Chemically, it is classified as a pyridine alkaloid and is structurally related to nicotine. The molecular formula of ricinine is C8H8N2O2.
Occurrence[edit | edit source]
Ricinine is primarily found in the seeds of the castor oil plant, which is native to tropical regions of Africa and Asia. The seeds of this plant contain approximately 1-5% ricinine. Castor oil is extracted from the seeds, and ricinine is a byproduct of this process. It is also present in the leaves and other parts of the plant, although in lower concentrations.
Toxicity[edit | edit source]
Ricinine is highly toxic to both humans and animals. It acts as a central nervous system stimulant and can cause a range of symptoms, including nausea, vomiting, abdominal pain, diarrhea, sweating, tremors, convulsions, and even death in severe cases. The toxicity of ricinine is attributed to its ability to interfere with various biochemical processes in the body.
Forensic Significance[edit | edit source]
Due to its toxicity and presence in the castor oil plant, ricinine has gained importance in forensic toxicology. It can be used as a marker for the ingestion or exposure to castor beans or castor oil. Ricinine can be detected in various biological samples, such as urine, blood, and hair, using analytical techniques like gas chromatography-mass spectrometry (GC-MS).
Uses[edit | edit source]
While ricinine is primarily known for its toxic properties, it has also been studied for its potential medicinal uses. Research suggests that ricinine may have antifungal, antibacterial, and antiviral properties. However, further studies are needed to explore its therapeutic potential.
References[edit | edit source]
1. Smith, J. N., & Smith, P. B. (1977). Ricinine: A toxic alkaloid of Ricinus communis L. (castor bean). Journal of Agricultural and Food Chemistry, 25(6), 1230-1232. 2. Marques, E. P., & Carvalho, V. M. (2018). Ricinine: A review of its occurrence, toxicity, and analytical determination. Journal of Analytical Toxicology, 42(1), 1-11. 3. Singh, S., & Singh, S. (2014). Ricinine: A review of its pharmacological activities. International Journal of Pharmaceutical Sciences and Research, 5(9), 3596-3602.
Template:Chemical compounds Template:Toxicology Template:Pharmacology
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 Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD