CHEBI:75033 - peonidin chloride

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ChEBI Name peonidin chloride
ChEBI ID CHEBI:75033
Definition An anthocyanidin chloride that has peonidin as the cationic component.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Anonymous
Secondary ChEBI IDs CHEBI:7987
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Formula C16H13ClO6
Net Charge 0
Average Mass 336.72400
Monoisotopic Mass 336.040
InChI InChI=1S/C16H12O6.ClH/c1-21-15-4-8(2-3-11(15)18)16-13(20)7-10-12(19)5-9(17)6-14(10)22-16;/h2-7H,1H3,(H3-,17,18,19,20);1H
InChIKey OGBSHLKSHNAPEW-UHFFFAOYSA-N
SMILES [Cl-].COc1cc(ccc1O)-c1[o+]c2cc(O)cc(O)c2cc1O
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
apoptosis inducer
Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing peonidin chloride (CHEBI:75033) has part peonidin (CHEBI:75314)
peonidin chloride (CHEBI:75033) has role antineoplastic agent (CHEBI:35610)
peonidin chloride (CHEBI:75033) has role antioxidant (CHEBI:22586)
peonidin chloride (CHEBI:75033) has role apoptosis inducer (CHEBI:68495)
peonidin chloride (CHEBI:75033) has role metabolite (CHEBI:25212)
peonidin chloride (CHEBI:75033) is a anthocyanidin chloride (CHEBI:38696)
IUPAC Name
3,5,7-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromenium chloride
Synonyms Sources
3,4',5,7-tetrahydroxy-3'-methoxyflavylium chloride ChEBI
3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-1-benzopyrylium chloride KEGG COMPOUND
Peonidin KEGG COMPOUND
Database Links Databases
C08726 KEGG COMPOUND
HMDB0005797 HMDB
Peonidin Wikipedia
View more database links
Registry Numbers Types Sources
134-01-0 CAS Registry Number KEGG COMPOUND
134-01-0 CAS Registry Number ChemIDplus
3924296 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
23419068 PubMed citation Europe PMC
23419638 PubMed citation Europe PMC
Last Modified
22 August 2013