CHEBI:59411 - (5α,22S,24R)-22-hydroxyergostan-3-one

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (5α,22S,24R)-22-hydroxyergostan-3-one
ChEBI ID CHEBI:59411
ChEBI ASCII Name (5alpha,22S,24R)-22-hydroxyergostan-3-one
Definition A brassinosteroid that is 6-deoxocathasterone in which the hydroxy group at position 3 has been oxidised to the corresponding ketone.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C28H48O2
Net Charge 0
Average Mass 416.67950
Monoisotopic Mass 416.36543
InChI InChI=1S/C28H48O2/c1-17(2)18(3)15-26(30)19(4)23-9-10-24-22-8-7-20-16-21(29)11-13-27(20,5)25(22)12-14-28(23,24)6/h17-20,22-26,30H,7-16H2,1-6H3/t18-,19+,20+,22+,23-,24+,25+,26+,27+,28-/m1/s1
InChIKey XGIZPVUTLMXXTK-VNSZYHACSA-N
SMILES [H][C@@]12CC[C@@]3([H])[C@]4([H])CC[C@]([H])([C@H](C)[C@@H](O)C[C@@H](C)C(C)C)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CCC(=O)C2
ChEBI Ontology
Outgoing (5α,22S,24R)-22-hydroxyergostan-3-one (CHEBI:59411) has parent hydride campestane (CHEBI:35518)
(5α,22S,24R)-22-hydroxyergostan-3-one (CHEBI:59411) is a 22-hydroxy steroid (CHEBI:36863)
(5α,22S,24R)-22-hydroxyergostan-3-one (CHEBI:59411) is a 3-oxo-5α-steroid (CHEBI:13601)
(5α,22S,24R)-22-hydroxyergostan-3-one (CHEBI:59411) is a brassinosteroid (CHEBI:22921)
IUPAC Name
(22S,24R)-22-hydroxy-5α-ergostan-3-one
Synonyms Sources
(22S)-22-hydroxy-5α-campestan-3-one MetaCyc
(22S,24R)-22-hydroxy-5α-ergostan-3-one UniProt
(22S,24R)-22-hydroxy-5α-ergostan-3-one ChEBI
(22S,24R)-22-Hydroxy-5alpha-ergostan-3-one KEGG COMPOUND
(5α,22S,24R)-22-hydroxyergostan-3-one ChEBI
22alpha-Hydroxy-5alpha-campestan-3-one KEGG COMPOUND
22S-hydroxy-5α-campestan-3-one LIPID MAPS
Manual Xrefs Databases
C00007520 KNApSAcK
C15797 KEGG COMPOUND
CPD-3946 MetaCyc
LMST01031117 LIPID MAPS
View more database links
Registry Numbers Types Sources
8005941 Beilstein Registry Number Beilstein
8005941 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
17138693 PubMed citation Europe PMC
Last Modified
28 March 2017