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| myricetin |
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| CHEBI:18152 |
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| A hexahydroxyflavone that is flavone substituted by hydroxy groups at positions 3, 3', 4', 5, 5' and 7. It has been isolated from the leaves of Myrica rubra and other plants. |
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This entity has been manually annotated by the ChEBI Team.
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CHEBI:44341, CHEBI:7053, CHEBI:14636
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Molfile
XML
SDF
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| 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 |
| IKMDFBPHZNJCSN-UHFFFAOYSA-N |
| Oc1cc(O)c2c(c1)oc(-c1cc(O)c(O)c(O)c1)c(O)c2=O |
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antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
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plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
food component
Any substance that is distributed in foodstuffs. It includes materials derived from plants or animals, such as vitamins or minerals, as well as environmental contaminants.
cyclooxygenase 1 inhibitor
A cyclooxygenase inhibitor that interferes with the action of cyclooxygenase 1.
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hypoglycemic agent
A drug which lowers the blood glucose level.
antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
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View more via ChEBI Ontology
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Outgoing
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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
food component
(CHEBI:78295)
myricetin
(CHEBI:18152)
has role
hypoglycemic agent
(CHEBI:35526)
myricetin
(CHEBI:18152)
has role
plant metabolite
(CHEBI:76924)
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)
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Incoming
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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)
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3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one
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3,3',4',5,5',7-Hexahydroxyflavone
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ChemIDplus
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3,5,7,3',4',5'-Hexahydroxyflavone
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KEGG COMPOUND
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Cannabiscetin
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ChemIDplus
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Myricetin
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KEGG COMPOUND
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Myricetol
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ChemIDplus
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332331
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Reaxys Registry Number
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Reaxys
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332331
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Beilstein Registry Number
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Beilstein
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529-44-2
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CAS Registry Number
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KEGG COMPOUND
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529-44-2
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CAS Registry Number
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ChemIDplus
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19407970
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PubMed citation
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Europe PMC
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19778600
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PubMed citation
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Europe PMC
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22482362
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PubMed citation
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Europe PMC
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23099505
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PubMed citation
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Europe PMC
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23232835
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PubMed citation
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Europe PMC
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23265454
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PubMed citation
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Europe PMC
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