CHEBI:28195 - 3α-hydroxy-5β-androstan-17-one

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ChEBI Name 3α-hydroxy-5β-androstan-17-one ChEBI ID CHEBI:28195 ChEBI ASCII Name 3alpha-hydroxy-5beta-androstan-17-one Definition An androstanoid that is 5β-androstane substituted by an α-hydroxy group at position 3 and an oxo group at position 17. It is a metabolite of testosterone in mammals. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:40622, CHEBI:20236, CHEBI:11904, CHEBI:1710 Supplier Information No supplier information found for this compound. Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Quinolinic acid (abbreviated QUIN or QA), also known as pyridine-2,3-dicarboxylic acid, is a dicarboxylic acid with a pyridine backbone. It is a colorless solid. It is the biosynthetic precursor to niacin. Quinolinic acid is a downstream product of the kynurenine pathway, which metabolizes the amino acid tryptophan. It acts as an NMDA receptor agonist. Quinolinic acid has a potent neurotoxic effect. Studies have demonstrated that quinolinic acid may be involved in many psychiatric disorders, neurodegenerative processes in the brain, as well as other disorders. Within the brain, quinolinic acid is only produced by activated microglia and macrophages. Read full article at Wikipedia Formula C19H30O2 Net Charge 0 Average Mass 290.44030 Monoisotopic Mass 290.22458 InChI InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3/t12-,13-,14+,15+,16+,18+,19+/m1/s1 InChIKey QGXBDMJGAMFCBF-BNSUEQOYSA-N SMILES [H][C@]12CC[C@@]3([H])[C@]4([H])CCC(=O)[C@@]4(C)CC[C@]3([H])[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): mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing 3α-hydroxy-5β-androstan-17-one (CHEBI:28195) has parent hydride 5β-androstane (CHEBI:20659) 3α-hydroxy-5β-androstan-17-one (CHEBI:28195) has role human metabolite (CHEBI:77746) 3α-hydroxy-5β-androstan-17-one (CHEBI:28195) has role mouse metabolite (CHEBI:75771) 3α-hydroxy-5β-androstan-17-one (CHEBI:28195) is a 17-oxo steroid (CHEBI:19168) 3α-hydroxy-5β-androstan-17-one (CHEBI:28195) is a 3α-hydroxy steroid (CHEBI:36835) 3α-hydroxy-5β-androstan-17-one (CHEBI:28195) is a androstanoid (CHEBI:50402) Incoming 3α-hydroxy-5β-androstan-17-one 3-glucosiduronic acid (CHEBI:37451) has functional parent 3α-hydroxy-5β-androstan-17-one (CHEBI:28195) IUPAC Name 3α-hydroxy-5β-androstan-17-one Synonyms Sources (3α,5β)-3-hydroxyandrostan-17-one NIST Chemistry WebBook 3α-etiocholanolone NIST Chemistry WebBook 3alpha-Hydroxy-5beta-androstan-17-one KEGG COMPOUND 3α-hydroxy-5β-androstan-17-one UniProt 3alpha-Hydroxyetiocholan-17-one KEGG COMPOUND 5-isoandrosterone ChemIDplus 5β-androstan-3α-ol-17-one NIST Chemistry WebBook 5β-androsterone NIST Chemistry WebBook AETIOCHOLANOLONE PDBeChem Etiocholan-3alpha-ol-17-one KEGG COMPOUND Etiocholanolone ChemIDplus Manual Xrefs Databases AE2 PDBeChem C04373 KEGG COMPOUND DB02854 DrugBank Etiocholanolone Wikipedia HMDB0000490 HMDB LMST02020059 LIPID MAPS View more database links Registry Numbers Types Sources 2217625 Reaxys Registry Number Reaxys 53-42-9 CAS Registry Number KEGG COMPOUND 53-42-9 CAS Registry Number NIST Chemistry WebBook 53-42-9 CAS Registry Number ChemIDplus Citations Types Sources 1146492 PubMed citation Europe PMC 301822 PubMed citation Europe PMC 663966 PubMed citation Europe PMC Last Modified 18 October 2017