Lupeol

Lupeol
Names
	IUPAC name (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol
	Other names (3β,13ξ)-Lup-20(29)-en-3-ol; Clerodol; Monogynol B; Fagarasterol; Farganasterol
Identifiers
CAS Number	545-47-1 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL289191;
ChemSpider	23089061;
ECHA InfoCard	100.008.082
PubChem CID	259846;
UNII	O268W13H3O ;
	InChI InChI=1S/C30H50O/c1-19(2)20-11-14-27(5)17-18-29(7)21(25(20)27)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h20-25,31H,1,9-18H2,2-8H3/t20-,21?,22-,23+,24-,25+,27+,28-,29+,30+/m0/s1;
	SMILES CC([C@@H]1CC[C@@]2(C)[C@@]1([H])[C@@]3([H])CC[C@]4([H])[C@@]5(C)CC[C@H](O)C(C)(C)[C@]5([H])CC[C@@]4(C)[C@]3(C)CC2)=C;
Properties
Chemical formula	C30H50O
Molar mass	426.729 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Lupeol is a pharmacologically active pentacyclic triterpenoid. It has several potential medicinal properties, like anticancer and anti-inflammatory activity.^[1]

^ Majumder, Soumya; Ghosh, Arindam; Bhattacharya, Malay (2020-08-27). "Natural anti-inflammatory terpenoids in Camellia japonica leaf and probable biosynthesis pathways of the metabolome". Bulletin of the National Research Centre. 44 (1): 141. doi:10.1186/s42269-020-00397-7. ISSN 2522-8307.

[:0-1] Majumder, Soumya; Ghosh, Arindam; Bhattacharya, Malay (2020-08-27). "Natural anti-inflammatory terpenoids in Camellia japonica leaf and probable biosynthesis pathways of the metabolome". Bulletin of the National Research Centre. 44 (1): 141. doi:10.1186/s42269-020-00397-7. ISSN 2522-8307.

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