Lophenol

Lophenol
Names
	IUPAC name (3S,4S,5S,9R,10S,13R,14R,17R)-4,10,13-trimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
Identifiers
CAS Number	481-25-4 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:18378;
ChemSpider	141024;
KEGG	C08825;
PubChem CID	160482;
UNII	X4BL075LYS;
CompTox Dashboard (EPA)	DTXSID70963996 ;
	InChI InChI=1S/C28H48O/c1-18(2)8-7-9-19(3)22-12-13-24-21-10-11-23-20(4)26(29)15-17-28(23,6)25(21)14-16-27(22,24)5/h10,18-20,22-26,29H,7-9,11-17H2,1-6H3/t19-,20+,22-,23+,24+,25+,26+,27-,28+/m1/s1 Key: LMYZQUNLYGJIHI-SPONXPENSA-N;
	SMILES C[C@@H]1[C@H](CC[C@]2([C@H]1CC=C3[C@@H]2CC[C@]4([C@H]3CC[C@@H]4[C@H](C)CCCC(C)C)C)C)O;
Properties
Chemical formula	C28H48O
Molar mass	400.691 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

Lophenol, or 4α-methyllathosterol, also called 4-Methylcholest-7-en-3-ol, is a Metabolic intermediate of plant sterol biosynthesis.^[1]

References[edit]

^ Ullah, H; Khan, A; Rehman, NU; Halim, SA; Khan, H; Khan, I; Csuk, R; Al-Rawahi, A; Al-Hatmi, S; Al-Harrasi, A (24 April 2020). "Lophenol and lathosterol from resin of Commiphora kua possess hepatoprotective effects in vivo". Journal of Ethnopharmacology. 252: 112558. doi:10.1016/j.jep.2020.112558. PMID 31926985. S2CID 210166705.

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