
Myricetin >=96,0% - 10 Mg - Sigma
Código: 23969
Myricetin
≥96.0%, crystalline
Sinônimo(s):
3,3′,4′,5,5′,7-Hexahydroxyflavone, Cannabiscetin, Myricetol
About This Item
Fórmula empírica (Notação de Hill):
C15H10O8
CAS Number:
Peso molecular:
318.24
Beilstein:
332331
Número CE:
Número MDL:
Código UNSPSC:
12352202
ID de substância PubChem:
NACRES:
NA.77
Nível de qualidade
Ensaio
≥96.0%
Formulário
crystalline
pf
>300 °C (lit.)
solubilidade
absolute ethanol: 10 mg/mL, clear to slightly hazy, yellow to very deep greenish-yellow
cadeia de caracteres 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
chave InChI
IKMDFBPHZNJCSN-UHFFFAOYSA-N
Informações sobre genes
human ... CYP1A2(1544)
mouse ... Hexa(15211)
rat ... Il4(287287), Tnf(24835)
Aplicação
Myricetin has been used:
-
to investigate its effect on end product (AGE)- bovine serum albumin mediated phosphorylation of mitogen-activated protein kinase(ERK1) [1]
-
as a standard for the quantification of phenolics from noni plant extracts using high performance liquid chromatography(HPLC)[2]
-
as a standard for characterization of phenolic compounds from Hibiscus sabdariffa using ultra-high performance liquid chromatography(UHPLC)[3]
Ações bioquímicas/fisiológicas
Myricetin is a naturally occurring flavonol with antioxidant property. It displays moderate membrane permeability and it degrades rapidly at elevated pH.[4] Myricetin is one of the major flavonoid present in edible plants and has anticarcinogenic and antimutagenic functionality.[5] It comprises of two benzene rings A and B. Ring B intercalates with nucleotide staking and inhibits bacterial DNA synthesis.[6] Myricetin elicits protective function against oxidative stress generated by tert-butylhydroperoxide (t-BHP) in diabetic rat and improves glutathione peroxidase (GPx) and xanthine oxidase (XO) enzyme activity. It also lowers the glycation of low-density lipoprotein.[1]