Lichesterol

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

Lichesterol
Names
IUPAC name
(22E)-Ergosta-5,8,22-trien-3β-ol
Preferred IUPAC name
(1R,3aR,7S,9aS,11aR)-1-[(2R,3E,5R)-5,6-Dimethylhept-3-en-2-yl]-9a,11a-dimethyl-2,3,3a,4,6,7,8,9,9a,10,11,11a-dodecahydro-1H-cyclopenta[a]phenanthren-7-ol
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
  • 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
  • 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
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

References
  1. 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. doi:10.1007/BF00486063. PMID 4282021. S2CID 36287225.


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