CHEBI:16229 - 3β-hydroxy-5β-pregnan-20-one

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ChEBI Name 3β-hydroxy-5β-pregnan-20-one ChEBI ID CHEBI:16229 ChEBI ASCII Name 3beta-hydroxy-5beta-pregnan-20-one Definition The 3β-stereoisomer of 3-hydroxy-5β-pregnan-20-one. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:1721, CHEBI:11910 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 C21H34O2 Net Charge 0 Average Mass 318.49346 Monoisotopic Mass 318.25588 InChI InChI=1S/C21H34O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h14-19,23H,4-12H2,1-3H3/t14-,15+,16+,17-,18+,19+,20+,21-/m1/s1 InChIKey AURFZBICLPNKBZ-GRWISUQFSA-N SMILES [H][C@]12CC[C@@]3([H])[C@]4([H])CC[C@]([H])(C(C)=O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@H](O)C2 Metabolite of Species Details Mus musculus (NCBI:txid10090) See: PubMed Homo sapiens (NCBI:txid9606) See: PubMed 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 3β-hydroxy-5β-pregnan-20-one (CHEBI:16229) has role human metabolite (CHEBI:77746) 3β-hydroxy-5β-pregnan-20-one (CHEBI:16229) has role mouse metabolite (CHEBI:75771) 3β-hydroxy-5β-pregnan-20-one (CHEBI:16229) is a 3β-hydroxy steroid (CHEBI:36836) 3β-hydroxy-5β-pregnan-20-one (CHEBI:16229) is a 3-hydroxy-5β-pregnan-20-one (CHEBI:50171) Incoming 5β-pregnane-3β,20α-diol (CHEBI:156526) has functional parent 3β-hydroxy-5β-pregnan-20-one (CHEBI:16229) IUPAC Name 3β-hydroxy-5β-pregnan-20-one Synonyms Sources (3β,5β)-3-hydroxypregnan-20-one NIST Chemistry WebBook 3beta-Hydroxy-5beta-pregnane-20-one KEGG COMPOUND 3β-hydroxy-5β-pregnane-20-one UniProt 3β-hydroxy-5β-tetrahydroprogesterone NIST Chemistry WebBook epipregnanolone NIST Chemistry WebBook Manual Xrefs Databases C11825 KEGG COMPOUND HMDB0001471 HMDB LMST02030185 LIPID MAPS View more database links Registry Numbers Types Sources 128-21-2 CAS Registry Number NIST Chemistry WebBook 128-21-2 CAS Registry Number ChemIDplus 3035289 Reaxys Registry Number Reaxys 3035289 Beilstein Registry Number Beilstein Citations Types Sources 1265794 PubMed citation Europe PMC 17583491 PubMed citation Europe PMC 347637 PubMed citation Europe PMC Last Modified 18 October 2017