From Surf Wiki (app.surf) — the open knowledge base
Furanolactone
A furanolactone is a heterocyclic chemical compound that contains both lactone and furan rings in its chemical structure.
Examples include:
- The salvinorins, including the hallucinogenic compound salvinorin A
- Columbin, a bitter diterpenoid from Calumbae Radix
- Limonoids such as limonin, nomilin, and nomilinic acid
- Tinosporide, a diterpenoid originally isolated from Tinospora cordifolia
References
References
- (2006). "Synthetic studies of neoclerodane diterpenes from Salvia divinorum: selective modification of the furan ring". Bioorg Med Chem Lett.
- (2002). "A bitter diterpenoid furanolactone columbin from Calumbae Radix inhibits azoxymethane-induced rat colon carcinogenesis". Cancer Lett.
- (1989). "Structure of columbin, a diterpenoid furanolactone from Tinospora cordifolia Miers". Acta Crystallogr C.
- (1989). "Structure of tinosporide, a diterpenoid furanolactone from Tinospora cordifolia Miers". Acta Crystallographica Section C.
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about Furanolactone — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report