20S-Hydroxycholesterol

20S-Hydroxycholesterol

File:20S-hydroxycholesterol.svg
Names
IUPAC name Cholest-5-ene-3β,20-diol
Systematic IUPAC name (1S,3aS,3bS,7S,9aR,9bS,11aS)-1-[(2S)-2-Hydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-2,3,3a,3b,4,6,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-cyclopenta[a]phenanthren-7-ol
Other names 20α-Hydroxycholesterol; 5-Cholestene-3β,20α-diol; 20(S)-OHC
Identifiers
CAS Number	516-72-3
3D model (JSmol)	Interactive image
ChEBI	CHEBI:166801
ChemSpider	24823271
ECHA InfoCard
E number
PubChem CID	24779600
UNII	30060WAL99
CompTox Dashboard (EPA)	{{#property:P3117}}
InChI InChI=1S/C27H46O2/c1-18(2)7-6-14-27(5,29)24-11-10-22-21-9-8-19-17-20(28)12-15-25(19,3)23(21)13-16-26(22,24)4/h8,18,20-24,28-29H,6-7,9-17H2,1-5H3/t20-,21?,22?,23?,24-,25-,26-,27-/m0/s1 Key: MCKLJFJEQRYRQT-BEOVMOENSA-N
SMILES CC(C)CCC[C@@](C)([C@H]1CCC2[C@@]1(CCC3C2CC=C4[C@@]3(CC[C@@H](C4)O)C)C)O
Properties
Chemical formula	C27H46O2
Molar mass	402.663 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

20S-Hydroxycholesterol is a steroid of the oxysterol class. It is a human metabolite of cholesterol.

20S-Hydroxycholesterol has been the subject of research into its role in human health. For example, 20S-hydroxycholesterol has been found to be an allosteric activator of the Hedgehog signaling pathway, which has implications in cancer research.

More recently, 20S-hydroxycholesterol was identified as an endogenous ligand for the sigma-2 receptor, which had previously been considered an orphan receptor since its discovery in 1990.