CHEBI:78600 - 11-dehydrocorticosterone

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ChEBI Name 11-dehydrocorticosterone ChEBI ID CHEBI:78600 Definition An 11-oxo steroid that is corticosterone in which the hydroxy substituent at the 11β position has been oxidised to give the corresponding ketone. Stars This entity has been manually annotated by the ChEBI Team. Submitter Lucila Aimo Secondary ChEBI IDs CHEBI:711 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 C21H28O4 Net Charge 0 Average Mass 344.44460 Monoisotopic Mass 344.19876 InChI InChI=1S/C21H28O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-16,19,22H,3-8,10-11H2,1-2H3/t14-,15-,16+,19+,20-,21-/m0/s1 InChIKey FUFLCEKSBBHCMO-KJQYFISQSA-N SMILES C[C@]12CC(=O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO Metabolite of Species Details Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 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 11-dehydrocorticosterone (CHEBI:78600) has functional parent corticosterone (CHEBI:16827) 11-dehydrocorticosterone (CHEBI:78600) has role human metabolite (CHEBI:77746) 11-dehydrocorticosterone (CHEBI:78600) has role mouse metabolite (CHEBI:75771) 11-dehydrocorticosterone (CHEBI:78600) is a 11-oxo steroid (CHEBI:47787) 11-dehydrocorticosterone (CHEBI:78600) is a 20-oxo steroid (CHEBI:36885) 11-dehydrocorticosterone (CHEBI:78600) is a 21-hydroxy steroid (CHEBI:35344) 11-dehydrocorticosterone (CHEBI:78600) is a 3-oxo-Δ4 steroid (CHEBI:47909) 11-dehydrocorticosterone (CHEBI:78600) is a corticosteroid (CHEBI:50858) 11-dehydrocorticosterone (CHEBI:78600) is a primary α-hydroxy ketone (CHEBI:139590) Synonyms Sources 11-dehydrocorticosterone UniProt 11-DHC ChEBI 11-oxo-11-deoxycorticosterone ChemIDplus 17-(1-keto-2-hydroxyethyl)-Δ4androsten-3,11-dione ChEBI 17-deoxycortisone ChemIDplus 4-pregnen-21-ol- 3,11,20-trione SUBMITTER dehydrocorticosterone ChemIDplus Δ4-pregnen-21-ol-3,11,20-trione ChEBI Kendall's compound A ChemIDplus Manual Xrefs Databases C05490 KEGG COMPOUND HMDB0004029 HMDB LMST02030192 LIPID MAPS US2778776 Patent View more database links Registry Numbers Types Sources 3108660 Reaxys Registry Number Reaxys 72-23-1 CAS Registry Number KEGG COMPOUND 72-23-1 CAS Registry Number ChemIDplus Citations Types Sources 11751610 PubMed citation Europe PMC 17329828 PubMed citation Europe PMC 17389675 PubMed citation Europe PMC 1951719 PubMed citation Europe PMC 23832962 PubMed citation Europe PMC 4295227 PubMed citation Europe PMC 8430442 PubMed citation Europe PMC 8498539 PubMed citation Europe PMC 8613810 PubMed citation Europe PMC Last Modified 06 February 2018