Lichesterol

Lichesterol
Names
	IUPAC name (3β,22E)-Ergosta-5,8,22-trien-3-ol
	Systematic IUPAC name (3β,22E)-Ergosta-5,8,22-trien-3-ol
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	4444706;
KEGG	C08823;
PubChem CID	5281329;
CompTox Dashboard (EPA)	DTXSID101045666 ;
	InChI InChI=1S/C28H44O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-9,18-20,22,24-25,29H,10-17H2,1-6H3/b8-7+/t19-,20+,22-,24+,25-,27-,28+/m0/s1 Key: VILFZDAFELACSG-CMNOFMQQSA-N; InChI=1/C28H44O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-9,18-20,22,24-25,29H,10-17H2,1-6H3/b8-7+/t19-,20+,22-,24+,25-,27-,28+/m0/s1 Key: VILFZDAFELACSG-CMNOFMQQBH;
	SMILES C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CCC3=C2CC=C4[C@@]3(CC[C@@H](C4)O)C)C;
Properties
Chemical formula	C28H44O
Molar mass	396.648
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Lichesterol is a sterol made by certain fungi and lichens.^[1]

References

^ Morris, DC; Safe, S; Subden, RE (1974). "Detection of the ergosterol and episterol isomers lichesterol and fecosterol in nystatin-resistant mutants of Neurospora crassa". Biochemical genetics. 12 (6): 459–66. PMID 4282021.

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