CHEBI:102029 - sorbinil

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ChEBI Name sorbinil
ChEBI ID CHEBI:102029
Definition An azaspiro compound having a monofluoro-substituted chromane skeleton spiro-linked to an imidazolidinedione ring.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:45392
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Formula C11H9FN2O3
Net Charge 0
Average Mass 236.19920
Monoisotopic Mass 236.05972
InChI InChI=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
InChIKey LXANPKRCLVQAOG-NSHDSACASA-N
SMILES Fc1ccc2OCC[C@]3(NC(=O)NC3=O)c2c1
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): 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).
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ChEBI Ontology
Outgoing 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 Sources
sorbinil ChemIDplus
sorbinilo ChemIDplus
sorbinilum ChemIDplus
Synonyms Sources
(S)-6-Fluorospiro(chroman-4,4'-imidazolidine)-2',5'-dione ChemIDplus
sorbinol ChEBI
Manual Xrefs Databases
DB02712 DrugBank
DE2821966 Patent
SBI PDBeChem
Sorbinil Wikipedia
US4130714 Patent
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Registry Numbers Types Sources
4297401 Reaxys Registry Number Reaxys
68367-52-2 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
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Last Modified
12 June 2018