Chemistry:Friedelane

From HandWiki

Friedelane is an aliphatic chemical compound and natural product. Its formula is C
30H
52.[1] Friedelane is a triterpene, and it and similar compounds are found in several plants.[2] One such compound found in the bark of cork oak, friedelin, is considered a "friedelane-like",[3] and has noted antimicrobial properties.[4] It is also a biological precursor of celastrol.[5]

Occurrence

Friedelane is found in the wood of Calophyllum tomentosum,[6] as well as the flowers of Pongamia pinnata.[7]

References

  1. ↑ Template:Cite PubChem
  2. ↑ Chávez, H.; Estévez-Braun, A.; Ravelo, A. G.; González, A. G. (1998-01-01). "Friedelane Triterpenoids from Maytenus macrocarpa". Journal of Natural Products 61 (1): 82–85. doi:10.1021/np970232k. ISSN 0163-3864. 
  3. ↑ Yaghoobi Anzabi, Mohadese; Cmoch, Piotr; Luboradzki, Roman; Pakulski, Zbigniew (2024-01-01). "Selective transformations of friedelanes isolated from cork smoker wash solids". Steroids 201. doi:10.1016/j.steroids.2023.109333. ISSN 0039-128X. https://www.sciencedirect.com/science/article/pii/S0039128X23001617. 
  4. ↑ Аrbаin, Dаyаr; Saputri, Gita Ayu; Syahputra, Ghalib Syukrilah; Widiyastuti, Yuli; Susanti, Deny; Taher, Muhammad (2021-10-05). "Genus Pterocarpus: A review of ethnopharmacology, phytochemistry, biological activities, and clinical evidence". Journal of Ethnopharmacology 278. doi:10.1016/j.jep.2021.114316. ISSN 0378-8741. https://www.sciencedirect.com/science/article/pii/S0378874121005432. 
  5. ↑ Lu, Yun; Luo, Yunfeng; Zhou, Jiawei; Hu, Tianyuan; Tu, Lichan; Tong, Yuru; Su, Ping; Liu, Yuan et al. (2022). "Probing the functions of friedelane‐type triterpene cyclases from four celastrol‐producing plants" (in en). The Plant Journal 109 (3): 555–567. doi:10.1111/tpj.15575. ISSN 0960-7412. https://onlinelibrary.wiley.com/doi/10.1111/tpj.15575. 
  6. ↑ Karunanayake, Subadra; Sotheeswaran, Subramanian; Uvais, M.; Sultanbawa, S.; Balasubramaniam, Sinnathamby (1981-01-01). "Xanthones and triterpenes of Calophyllum tomentosum". Phytochemistry 20 (6): 1303–1304. doi:10.1016/0031-9422(81)80026-X. ISSN 0031-9422. https://www.sciencedirect.com/science/article/pii/003194228180026X. 
  7. ↑ Talapatra, Sunil K.; Mallik, Asok K.; Talapatra, Bani (1982-01-01). "Isopongaglabol and 6-methoxyisopongaglabol, two new hydroxyfuranoflavones from Pongamia glabra". Phytochemistry 21 (3): 761–766. doi:10.1016/0031-9422(82)83183-X. ISSN 0031-9422. https://www.sciencedirect.com/science/article/pii/003194228283183X. 




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