CHEBI:28324 - 11-deoxycortisol

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ChEBI Name 11-deoxycortisol
ChEBI ID CHEBI:28324
Definition A deoxycortisol that is cortisol in which the hydroxy group at position 11 has been replaced by a hydrogen.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:19124, CHEBI:714
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Formula C21H30O4
Net Charge 0
Average Mass 346.46050
Monoisotopic Mass 346.214
InChI InChI=1S/C21H30O4/c1-19-8-5-14(23)11-13(19)3-4-15-16(19)6-9-20(2)17(15)7-10-21(20,25)18(24)12-22/h11,15-17,22,25H,3-10,12H2,1-2H3/t15-,16+,17+,19+,20+,21+/m1/s1
InChIKey WHBHBVVOGNECLV-OBQKJFGGSA-N
SMILES [H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@@]1(C)[C@@]2([H])CC[C@]1(O)C(=O)CO
Metabolite of Species Details
Mus musculus (NCBI:10090) Source: BioModels - MODEL1507180067 See: PubMed
Homo sapiens (NCBI:9606) 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).
hormone
Originally referring to an endogenous compound that is formed in specialized organ or group of cells and carried to another organ or group of cells, in the same organism, upon which it has a specific regulatory function, the term is now commonly used to include non-endogenous, semi-synthetic and fully synthetic analogues of such compounds.
(via steroid hormone )
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ChEBI Ontology
Outgoing 11-deoxycortisol (CHEBI:28324) has role human metabolite (CHEBI:77746)
11-deoxycortisol (CHEBI:28324) has role mouse metabolite (CHEBI:75771)
11-deoxycortisol (CHEBI:28324) is a deoxycortisol (CHEBI:23618)
11-deoxycortisol (CHEBI:28324) is a glucocorticoid (CHEBI:24261)
IUPAC Name
17,21-dihydroxypregn-4-ene-3,20-dione
Synonyms Sources
11-Deoxycortisol KEGG COMPOUND
11-deoxycortisol UniProt
11-desoxy-17-hydroxycorticosterone ChemIDplus
cortodoxone ChemIDplus
Cortodoxone KEGG COMPOUND
Database Links Databases
C05488 KEGG COMPOUND
Cortexolone Wikipedia
D03595 KEGG DRUG
HMDB0000015 HMDB
LMST02030086 LIPID MAPS
View more database links
Registry Numbers Types Sources
152-58-9 CAS Registry Number KEGG COMPOUND
152-58-9 CAS Registry Number ChemIDplus
2511358 Beilstein Registry Number Beilstein
2511358 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
18958601 PubMed citation Europe PMC
24863084 PubMed citation Europe PMC
Last Modified
27 January 2016