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> Main
CHEBI:102029 - sorbinil
Main
ChEBI Ontology
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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
Supplier Information
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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).
View more via ChEBI Ontology
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
(4
S
)-
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
View more database links
Registry Numbers
Types
Sources
4297401
Reaxys Registry Number
Reaxys
68367-52-2
CAS Registry Number
ChemIDplus
Citations
Types
Sources
10875546
PubMed citation
Europe PMC
10933817
PubMed citation
Europe PMC
11048957
PubMed citation
Europe PMC
11900277
PubMed citation
Europe PMC
18772236
PubMed citation
Europe PMC
19821053
PubMed citation
Europe PMC
20138035
PubMed citation
Europe PMC
20308528
PubMed citation
Europe PMC
20354121
PubMed citation
Europe PMC
21129963
PubMed citation
Europe PMC
29438107
PubMed citation
Europe PMC
7564101
PubMed citation
Europe PMC
7591626
PubMed citation
Europe PMC
8159110
PubMed citation
Europe PMC
8692029
PubMed citation
Europe PMC
9007520
PubMed citation
Europe PMC
9088040
PubMed citation
Europe PMC
9195881
PubMed citation
Europe PMC
9349546
PubMed citation
Europe PMC
Last Modified
12 June 2018