CHEBI:28113 - 24,25-dihydrolanosterol

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ChEBI Name 24,25-dihydrolanosterol ChEBI ID CHEBI:28113 Definition A 3β-sterol formed from lanosterol by reduction across the C-24‒C-25 double bond. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:1303, CHEBI:19807 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 C30H52O Net Charge 0 Average Mass 428.73328 Monoisotopic Mass 428.40182 InChI InChI=1S/C30H52O/c1-20(2)10-9-11-21(3)22-14-18-30(8)24-12-13-25-27(4,5)26(31)16-17-28(25,6)23(24)15-19-29(22,30)7/h20-22,25-26,31H,9-19H2,1-8H3/t21-,22-,25+,26+,28-,29-,30+/m1/s1 InChIKey MBZYKEVPFYHDOH-BQNIITSRSA-N SMILES [H][C@@]1(CC[C@@]2(C)C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)C(C)(C)[C@]1([H])CC3)[C@H](C)CCCC(C)C 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 24,25-dihydrolanosterol (CHEBI:28113) has functional parent lanosterol (CHEBI:16521) 24,25-dihydrolanosterol (CHEBI:28113) has role human metabolite (CHEBI:77746) 24,25-dihydrolanosterol (CHEBI:28113) has role mouse metabolite (CHEBI:75771) 24,25-dihydrolanosterol (CHEBI:28113) is a 3β-sterol (CHEBI:35348) 24,25-dihydrolanosterol (CHEBI:28113) is a tetracyclic triterpenoid (CHEBI:26893) Incoming eburicol (CHEBI:70315) has functional parent 24,25-dihydrolanosterol (CHEBI:28113) IUPAC Name lanost-8-en-3β-ol Synonyms Sources 24,25-Dihydrolanosterol KEGG COMPOUND 24,25-dihydrolanosterol UniProt Lanostenol ChemIDplus Manual Xrefs Databases C00023781 KNApSAcK C05109 KEGG COMPOUND CPD-8606 MetaCyc HMDB0006839 HMDB LMST01010087 LIPID MAPS View more database links Registry Numbers Types Sources 2224904 Beilstein Registry Number Beilstein 2224904 Reaxys Registry Number Reaxys 79-62-9 CAS Registry Number KEGG COMPOUND 79-62-9 CAS Registry Number ChemIDplus Citation Type Source 898228 PubMed citation Europe PMC Last Modified 03 October 2017