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CHEBI:102029 - sorbinil

ChEBI IDCHEBI:102029
ChEBI Namesorbinil
Stars
DefinitionAn azaspiro compound having a monofluoro-substituted chromane skeleton spiro-linked to an imidazolidinedione ring.
Secondary ChEBI IDCHEBI:45392
Last Modified12 June 2018
DownloadsMolfile
FormulaC11H9FN2O3
Net Charge0
Average Mass236.202
Monoisotopic Mass236.05972
SMILESO=C1NC(=O)[C@@]2(CCOc3ccc(F)cc32)N1
InChIInChI=1S/C11H9FN2O3/c12-6-1-2-8-7(5-6)11(3-4-17-8)9(15)13-10(16)14-11/h1-2,5H,3-4H2,(H2,13,14,15,16)/t11-/m0/s1
InChIKeyLXANPKRCLVQAOG-NSHDSACASA-N
Wikipedia
Roles Classification
Chemical Role:
antioxidant  A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role:
EC 1.1.1.21 (aldehyde reductase) inhibitor  An EC 1.1.1.* (oxidoreductase acting on donor CH-OH group, NAD+ or NADP+ acceptor) inhibitor that interferes with the action of aldehyde reductase (EC 1.1.1.21).
ChEBI Ontology
Outgoing Relation(s)
sorbinil (CHEBI:102029) has role antioxidant (CHEBI:22586)
sorbinil (CHEBI:102029) has role EC 1.1.1.21 (aldehyde reductase) inhibitor (CHEBI:48550)
sorbinil (CHEBI:102029) is a azaspiro compound (CHEBI:35624)
sorbinil (CHEBI:102029) is a chromanes (CHEBI:23230)
sorbinil (CHEBI:102029) is a imidazolidinone (CHEBI:55370)
sorbinil (CHEBI:102029) is a organofluorine compound (CHEBI:37143)
sorbinil (CHEBI:102029) is a oxaspiro compound (CHEBI:37948)
IUPAC Name 
(4S)-6-fluoro-2,3-dihydro-2'H,5'H-spiro[chromene-4,4'-imidazolidine]-2',5'-dione
INNs  Source
sorbinilumChemIDplus
sorbiniloChemIDplus
sorbinilChemIDplus
Synonyms  Source
(S)-6-Fluorospiro(chroman-4,4'-imidazolidine)-2',5'-dioneChemIDplus
sorbinolChEBI
Manual XrefsDatabases
SBIPDBeChem
SorbinilWikipedia
DE2821966Patent
US4130714Patent
DB02712DrugBank
Registry NumbersSources
Reaxys:4297401Reaxys
CAS:68367-52-2ChemIDplus
Citations