Weight | 318.237 g/mol |
---|---|
Formula | C15H10O8 |
Hydrogen Acceptors | 8 |
Hydrogen Donors | 6 |
Aromatic Rings | 3 |
Rotatable Bonds | 1 |
myricetin (529-44-2)
3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one
Score:
#513 in Biochemistry
,
#1598 in Biology
,
#1879 in Chemistry
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- Structural Determinants of Phosphoinositide 3-Kinase Inhibition by Wortmannin, LY294002, Quercetin, Myricetin, and Staurosporine (Molecular Cell, 2000)
- Flavonoid (Myricetin, Quercetin, Kaempferol, Luteolin, and Apigenin) Content of Edible Tropical Plants (Journal of Agricultural and Food Chemistry, 2001)
- Antioxidant and pro-oxidant actions of the plant phenolics quercetin, gossypol and myricetin: Effects on lipid peroxidation, hydroxyl radical generation and bleomycin-dependent damage to DNA (Biochemical Pharmacology, 1989)
- Content of the Flavonols Quercetin, Myricetin, and Kaempferol in 25 Edible Berries (Journal of Agricultural and Food Chemistry, 1999)
- Quercetin and myricetin protect against hydrogen peroxide-induced DNA damage (strand breaks and oxidised pyrimidines) in human lymphocytes. (Mutation Research-genetic Toxicology and Environmental Mutagenesis, 1997)
- Myricetin and quercetin, the flavonoid constituents ofGinkgo biloba extract, greatly reduce oxidative metabolism in both resting and Ca2+-loaded brain neurons (Brain Research, 1994)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one
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SMILESC1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
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InChIKeyIKMDFBPHZNJCSN-UHFFFAOYSA-N
- Pubchem - myricetin
- Wikipedia - myricetin
Myricetin is a member of the flavonoid class of polyphenolic compounds, with antioxidant properties. It is commonly derived from vegetables, fruits, nuts, berries, tea, and is also found in red wine. Myricetin is structurally similar to fisetin, luteolin, and quercetin and is reported to have many of the same functions as these other members of the flavonol class of flavonoids.
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