CHEBI:5202 - fustin

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ChEBI Name fustin
ChEBI ID CHEBI:5202
Definition A dihydroflavonol that is the 2,3-dihydro derivative of fisetin.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C15H12O6
Net Charge 0
Average Mass 288.255
Monoisotopic Mass 288.06339
InChI InChI=1S/C15H12O6/c16-8-2-3-9-12(6-8)21-15(14(20)13(9)19)7-1-4-10(17)11(18)5-7/h1-6,14-18,20H
InChIKey FNUPUYFWZXZMIE-UHFFFAOYSA-N
SMILES OC1C(OC2=C(C=CC(O)=C2)C1=O)C1=CC=C(O)C(O)=C1
Roles Classification
Biological Role(s): antiviral agent
A substance that destroys or inhibits replication of viruses.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
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ChEBI Ontology
Outgoing fustin (CHEBI:5202) has functional parent fisetin (CHEBI:42567)
fustin (CHEBI:5202) has role antiviral agent (CHEBI:22587)
fustin (CHEBI:5202) has role plant metabolite (CHEBI:76924)
fustin (CHEBI:5202) is a 4'-hydroxyflavanones (CHEBI:140331)
fustin (CHEBI:5202) is a dihydroflavonols (CHEBI:48039)
fustin (CHEBI:5202) is a secondary α-hydroxy ketone (CHEBI:2468)
fustin (CHEBI:5202) is a tetrahydroxyflavanone (CHEBI:38742)
Incoming fustin 3-O-β-D-galactoside (CHEBI:28183) has functional parent fustin (CHEBI:5202)
(−)-trans-fustin (CHEBI:228235) is a fustin (CHEBI:5202)
(+)-trans-fustin (CHEBI:228234) is a fustin (CHEBI:5202)
IUPAC Name
2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-2,3-dihydro-4H-chromen-4-one
Synonyms Sources
2,3-dihydrofisetin KEGG COMPOUND
2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-2,3-dihydro-4H-1-benzopyran-4-one IUPAC
3',4',7-trihydroxyflavanol ChEBI
3,3',4',7-tetrahydroxyflavanone ChemIDplus
3,7,3',4'-tetrahydroxyflavanone ChEBI
Manual Xref Database
Fustin Wikipedia
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Registry Number Type Source
101849-13-2 CAS Registry Number ChEBI
Citations Waiting for Citations Types Sources
13744045 PubMed citation Europe PMC
1384499 PubMed citation Europe PMC
17603285 PubMed citation Europe PMC
19533734 PubMed citation Europe PMC
22538659 PubMed citation Europe PMC
34660970 PubMed citation Europe PMC
34860003 PubMed citation Europe PMC
34866996 PubMed citation Europe PMC
35212538 PubMed citation Europe PMC
35847266 PubMed citation Europe PMC
36551777 PubMed citation Europe PMC
37520245 PubMed citation Europe PMC
Last Modified
20 November 2023
General Comment
2023-11-20 This is the entry for material with unspecified stereochemistry. There are separate entries for the racemate (±-trans-fustin) and its individual enantiomers, (+)- and (−)-trans-fustin.