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myricetin (CHEBI:18152)

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ChEBI Name myricetin
ChEBI ID CHEBI:18152
Definition A hexahydroxyflavone that is flavone substituted by hydroxy groups at positions 3, 3', 4', 5, 5' and 7.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:14636, CHEBI:7053
Supplier Information
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Formula Source
C15H10O8 KEGG COMPOUND
Net Charge 0
Average Mass 318.23510
InChI
InChI=1S/C15H10O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,16-20,22H
InChIKey
IKMDFBPHZNJCSN-UHFFFAOYSA-N
SMILES
Oc1cc(O)c2c(c1)oc(-c1cc(O)c(O)c(O)c1)c(O)c2=O
Roles Classification
Chemical Role(s): cyclooxygenase 1 inhibitor
A cyclooxygenase inhibitor that interferes with the action of cyclooxygenase 1.
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): cyclooxygenase 1 inhibitor
A cyclooxygenase inhibitor that interferes with the action of cyclooxygenase 1.
secondary metabolite
A metabolite that is not directly involved in the normal growth, development or reproduction of an organism.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more on the ChEBI Ontology
ChEBI Ontology
Outgoing myricetin (CHEBI:18152) has role antineoplastic agent (CHEBI:35610)
myricetin (CHEBI:18152) has role antioxidant (CHEBI:22586)
myricetin (CHEBI:18152) has role cyclooxygenase 1 inhibitor (CHEBI:50630)
myricetin (CHEBI:18152) has role secondary metabolite (CHEBI:26619)
myricetin (CHEBI:18152) is a 7-hydroxyflavonol (CHEBI:52267)
myricetin (CHEBI:18152) is a hexahydroxyflavone (CHEBI:24561)
myricetin (CHEBI:18152) is conjugate acid of myricetin(1−) (CHEBI:58395)
Incoming 3ʼ,5,7-trihydroxy-3,4ʼ,5ʼ-trimethoxyflavone (CHEBI:70009) has functional parent myricetin (CHEBI:18152)
3ʼ,5-dihydroxy-3,4ʼ,5ʼ,7-tetramethoxyflavone (CHEBI:70006) has functional parent myricetin (CHEBI:18152)
5,7,3ʼ,5ʼ-tetrahydroxy-3,4ʼ-dimethyoxyflavone (CHEBI:70004) has functional parent myricetin (CHEBI:18152)
combretol (CHEBI:70005) has functional parent myricetin (CHEBI:18152)
dihydromyricetin (CHEBI:28917) has functional parent myricetin (CHEBI:18152)
laricitrin (CHEBI:31763) has functional parent myricetin (CHEBI:18152)
myricetin 3-O-β-D-galactopyranoside (CHEBI:75815) has functional parent myricetin (CHEBI:18152)
myricetin 3-O-β-L-galactopyranoside (CHEBI:75817) has functional parent myricetin (CHEBI:18152)
myricetin O-glucoside (CHEBI:75812) has functional parent myricetin (CHEBI:18152)
myricetin O-glucuronide (CHEBI:75806) has functional parent myricetin (CHEBI:18152)
myricetin-3-O-β-D-xylopyranoside (CHEBI:69458) has functional parent myricetin (CHEBI:18152)
myricetin-3-O-arabinofuranoside (CHEBI:69459) has functional parent myricetin (CHEBI:18152)
myricitrin (CHEBI:70082) has functional parent myricetin (CHEBI:18152)
syringetin (CHEBI:18215) has functional parent myricetin (CHEBI:18152)
myricetin(1−) (CHEBI:58395) is conjugate base of myricetin (CHEBI:18152)
IUPAC Name
3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one
Synonyms Sources
3,3',4',5,5',7-Hexahydroxyflavone ChemIDplus
3,5,7,3',4',5'-Hexahydroxyflavone KEGG COMPOUND
Cannabiscetin ChemIDplus
Myricetin KEGG COMPOUND
Myricetol ChemIDplus
Database Links Databases
C10107 KEGG COMPOUND
DB02375 DrugBank
HMDB02755 HMDB
LMPK12110001 LIPID MAPS
Myricetin Wikipedia
MYRICETIN MetaCyc
View more database links
Registry Numbers Types Sources
332331 Reaxys Registry Number Reaxys
332331 Beilstein Registry Number Beilstein
529-44-2 CAS Registry Number KEGG COMPOUND
529-44-2 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
19407970 PubMed citation CiteXplore
19778600 PubMed citation CiteXplore
22482362 PubMed citation CiteXplore
23099505 PubMed citation CiteXplore
23232835 PubMed citation CiteXplore
23265454 PubMed citation CiteXplore
Last Modified
16 January 2014

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