CHEBI:16608 - 5α-cholest-8-en-3β-ol

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ChEBI Name 5α-cholest-8-en-3β-ol ChEBI ID CHEBI:16608 ChEBI ASCII Name 5alpha-cholest-8-en-3beta-ol Definition A cholestanoid that is 5α-cholestane substituted by a β-hydroxy group at position 3. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:12170, CHEBI:20645, CHEBI:2139 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C27H46O Net Charge 0 Average Mass 386.65354 Monoisotopic Mass 386.35487 InChI InChI=1S/C27H46O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-21,23-24,28H,6-17H2,1-5H3/t19-,20+,21+,23-,24+,26+,27-/m1/s1 InChIKey QETLKNDKQOXZRP-XTGBIJOFSA-N SMILES [H][C@@]12CCC3=C(CC[C@]4(C)[C@]([H])(CC[C@@]34[H])[C@H](C)CCCC(C)C)[C@@]1(C)CC[C@H](O)C2 Metabolite of Species Details Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed Homo sapiens (NCBI:txid9606) See: DOI Roles Classification Biological Role(s): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). View more via ChEBI Ontology ChEBI Ontology Outgoing 5α-cholest-8-en-3β-ol (CHEBI:16608) has parent hydride 5α-cholestane (CHEBI:35515) 5α-cholest-8-en-3β-ol (CHEBI:16608) has role human metabolite (CHEBI:77746) 5α-cholest-8-en-3β-ol (CHEBI:16608) has role mouse metabolite (CHEBI:75771) 5α-cholest-8-en-3β-ol (CHEBI:16608) is a 3β-sterol (CHEBI:35348) 5α-cholest-8-en-3β-ol (CHEBI:16608) is a cholestanoid (CHEBI:50401) IUPAC Name (5α)-cholest-8-en-3β-ol Synonyms Sources 5alpha-Cholest-8-en-3beta-ol KEGG COMPOUND 5alpha-cholest-8-en-3beta-ol ChEBI 5α-cholest-8-en-3β-ol ChEBI 5α-cholest-8-en-3β-ol UniProt Cholestenol KEGG COMPOUND Zymostenol KEGG COMPOUND Manual Xrefs Databases C03845 KEGG COMPOUND CPD-8621 MetaCyc HMDB0006841 HMDB LMST01010096 LIPID MAPS View more database links Registry Numbers Types Sources 2337227 Reaxys Registry Number Reaxys 566-97-2 CAS Registry Number KEGG COMPOUND 566-97-2 CAS Registry Number ChemIDplus Citation Type Source 5642322 PubMed citation Europe PMC Last Modified 19 October 2017