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20α,22R-Dihydroxycholesterol
Names
	IUPAC name (22R)-Cholest-5-ene-3β,20,22-triol
	Systematic IUPAC name (2R,3R)-2-[(1S,3aS,3bS,7S,9aR,9bS,11aS)-7-Hydroxy-9a,11a-dimethyl-2,3,3a,3b,4,6,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-cyclopenta[a]phenanthren-1-yl]-6-methylheptane-2,3-diol
Identifiers
CAS Number	596-94-1 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	2339391
ChEBI	CHEBI:1294;
ChEMBL	ChEMBL560194;
ChemSpider	4956189;
KEGG	C05501;
PubChem CID	6453841;
CompTox Dashboard (EPA)	DTXSID00975007 ;
	InChI InChI=1S/C27H46O3/c1-17(2)6-11-24(29)27(5,30)23-10-9-21-20-8-7-18-16-19(28)12-14-25(18,3)22(20)13-15-26(21,23)4/h7,17,19-24,28-30H,6,8-16H2,1-5H3/t19-,20-,21-,22-,23-,24+,25-,26-,27+/m0/s1 Key: ISBSSBGEYIBVTO-TYKWNDPBSA-N;
	SMILES CC(C)CC[C@H]([C@@](C)([C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O)C)C)O)O;
Properties
Chemical formula	C27H46O3
Molar mass	418.652 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

20α,22R-Dihydroxycholesterol, or (3β)-cholest-5-ene-3,20,22-triol is an endogenous, metabolic intermediate in the biosynthesis of the steroid hormones from cholesterol.^[1]^[2] Cholesterol ((3β)-cholest-5-en-3-ol) is hydroxylated by cholesterol side-chain cleavage enzyme (P450scc) to form 22R-hydroxycholesterol, which is subsequently hydroxylated again by P450scc to form 20α,22R-dihydroxycholesterol, and finally the bond between carbons 20 and 22 is cleaved by P450scc to form pregnenolone ((3β)-3-hydroxypregn-5-en-20-one),^[1]^[2] the precursor to the steroid hormones.