70050

Myricetin

≥96.0% (HPLC)

• Sinónimos: 3,3′,4′,5,5′,7-Hexahydroxyflavone, Cannabiscetin, Myricetol
• Fórmula empírica (notación de Hill): C₁₅H₁₀O₈
• Número de CAS: 529-44-2
• Peso molecular: 318.24
• Beilstein: 332331
• Número CE: 208-463-2
• Número MDL: MFCD00006827
• Código UNSPSC: 12352202
• ID de la sustancia en PubChem: 57652239
• NACRES: NA.77

Propiedades

• Ensayo: ≥96.0% (HPLC)
• Formulario: powder
• mp: ≥300 °C; >300 °C (lit.)
• solubilidad: ethanol: 10 mg/mL, clear to very faintly turbid, yellow to very deep greenish-yellow
• aplicaciones: metabolomics; vitamins, nutraceuticals, and natural products
• cadena SMILES: Oc1cc(O)c2C(=O)C(O)=C(Oc2c1)c3cc(O)c(O)c(O)c3
• 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
• Clave InChI: IKMDFBPHZNJCSN-UHFFFAOYSA-N
• Información sobre el gen: human ... CYP1A2(1544) ; mouse ... Hexa(15211) ; rat ... Il4(287287) , Tnf(24835)

Descripción

Descripción general

Myricetin (MYR) is a natural polyhydroxyflavonol compound, first isolated from the bark of Morella rubra (Myrica rubra) tree.[1]

Aplicación

Myricetin has been used:

• to study its preventive effect as an antioxidant on noise-induced hearing loss (NIHL) in rats[2]
• as a flavonoid compound to test antiviral activity of Bourbon virus (BRBV) and in inhibition of RNA-dependent RNA polymerase (RdRP)[3]
• to study its effect as a treatment on biofilms of Streptococcus mutans and Candida albicans[4]
• as a reference standard for the quantification of phenolic compounds from Juniperus species[5]

Acciones bioquímicas o fisiológicas

Myricetin exerts anti-oxidant effects[6], and anti-inflammatory effects by regulating multiple signal pathways.[1] It also displays anti-diabetic[1] and hepatoprotective effects.[6] Myricetin strongly inhibits yeast α-glucosidase,[7] glyoxalase I in vitro,[8] and bovine milk xanthine oxidase.[9] It also promotes complex formation between DNA and both topoisomerase I and II, an effect that may have implications in cancer chemotherapy.[10] Myricetin also has various nutraceuticals values and therapeutic effects.[1][6]

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Gloves, type N95 (US)