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Biological Data
| Biological description | Antioxidant flavonoid. Potentiates the cytotoxicity of natural killer cells. Shows a calcium channel/CaMK-II dependent modulation of GABAA receptor activity. Shows protective effects against diabetic nephrotoxicity, increases insulin signalling molecules and normalises carbohydrate metabolism products. |
Solubility & Handling
| Solubility overview | Soluble in ethanol (1mg/ml) or DMSO (5mg/ml) |
| Important | This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use. |
Chemical Data
| Chemical name | 3,3′,4′,5,5′,7-Hexahydroxyflavone |
| Chemical structure | ![Myricetin [529-44-2] Chemical Structure](data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAQAAAC1HAwCAAAAC0lEQVR4nGP6zwAAAgcBApocMXEAAAAASUVORK5CYII= "Myricetin [529-44-2]") |
| Molecular Formula | C15H10O8 |
| PubChem identifier | 5281672 |
| SMILES | C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O |
References for Myricetin
References are publications that support the biological activity of the product
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Protective effect of bioflavonoid myricetin enhances carbohydrate metabolic enzymes and insulin signaling molecules in streptozotocin-cadmium induced diabetic nephrotoxic rats.
Kandasamy N et al (2014) Toxicol Appl Pharmacol 279(2) : 173-85. -
Potentiation of natural killer cell activity with myricetin.
Lindqvist C et al (2014) Anticancer Res 34(8) : 3975-9.
![Myricetin [529-44-2] Chemical Structure](https://hellobio.com/media/catalog/product//h/b/hb0434.png "Myricetin [529-44-2]")
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