CHEBI:28103 - pinobanksin

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ChEBI Name pinobanksin
Definition A trihydroxyflavanone in which the three hydroxy substituents are located at positions 3, 5 and 7.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Anonymous
Secondary ChEBI IDs CHEBI:75149, CHEBI:8219, CHEBI:26136
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Formula C15H12O5
Net Charge 0
Average Mass 272.25280
InChI InChI=1S/C15H12O5/c16-9-6-10(17)12-11(7-9)20-15(14(19)13(12)18)8-4-2-1-3-5-8/h1-7,14-17,19H/t14-,15+/m0/s1
SMILES O[C@@H]1[C@H](Oc2cc(O)cc(O)c2C1=O)c1ccccc1
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides. In European countries, E-numbers for permitted antioxidant food additives are from E 300 to E 324.
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
An agent that reduces or interferes with the mutagenic actions or effects of a substance.
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ChEBI Ontology
Outgoing pinobanksin (CHEBI:28103) has role antimutagen (CHEBI:73190)
pinobanksin (CHEBI:28103) has role antioxidant (CHEBI:22586)
pinobanksin (CHEBI:28103) has role metabolite (CHEBI:25212)
pinobanksin (CHEBI:28103) is a trihydroxyflavanone (CHEBI:38739)
Synonyms Sources
2,3-Dihydro-3,5,7-trihydroxy-2-phenyl-4H-1-benzopyran-4-one ChemIDplus
3,5,7-Trihydroxyflavanone KEGG COMPOUND
Database Links Databases
C00000991 KNApSAcK
CPD-6992 MetaCyc
Pinobanksin Wikipedia
View more database links
Registry Numbers Types Sources
548-82-3 CAS Registry Number KEGG COMPOUND
548-82-3 CAS Registry Number ChemIDplus
91238 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
19636435 PubMed citation CiteXplore
23630255 PubMed citation CiteXplore
23870890 PubMed citation CiteXplore
9266597 PubMed citation CiteXplore
9725994 PubMed citation CiteXplore
IND44497441 Agricola citation CiteXplore
Last Modified
28 July 2014