| Weight | 464.379 g/mol |
|---|---|
| Formula | C21H20O12 |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 8 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
Myricitrin (17912-87-7)
3,3',4',5,5',7-hexahydroxyflavone 3-rhamnoside
Score:
#1033 in Neuroscience
,
#2222 in Biochemistry
,
#4497 in Biology
,
#5691 in Chemistry
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- Analysis of the Antinociceptive Effect of the Flavonoid Myricitrin: Evidence for a Role of the l-Arginine-Nitric Oxide and Protein Kinase C Pathways (Journal of Pharmacology and Experimental Therapeutics, 2005)
- Anti-allodynic property of flavonoid myricitrin in models of persistent inflammatory and neuropathic pain in mice. (Biochemical Pharmacology, 2006)
- The flavonoid glycosides, myricitrin, gossypin and naringin exert anxiolytic action in mice. (Neurochemical Research, 2009)
- Myricitrin as a substrate and inhibitor of myeloperoxidase: implications for the pharmacological effects of flavonoids. (Free Radical Biology and Medicine, 2008)
- Inhibitory effects of myricitrin on oxidative stress-induced endothelial damage and early atherosclerosis in ApoE-/- mice. (Toxicology and Applied Pharmacology, 2013)
- Antinociceptive action of myricitrin: involvement of the K+ and Ca2+ channels. (European Journal of Pharmacology, 2007)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,3',4',5,5',7-hexahydroxyflavone 3-rhamnoside
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SMILESCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O
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InChIKeyDCYOADKBABEMIQ-UHFFFAOYSA-N
- Pubchem - Myricitrin
- Wikipedia - Myricitrin
Myricitrin is a plant compound, the 3-O--L-rhamnopyranoside of myricetin.
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Myricitrin
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