A potent antioxidant
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Myricetin

Item No. 10012600

Technical Information
Formal Name
3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one
CAS Number
529-44-2
Synonyms
  • Cannabiscetin
  • LDN-0014058
  • NSC 407290
Molecular Formula
C15H10O8
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 10 mg/mlDMSO: 10 mg/mlDMSO:PBS (pH 7.2) (1:10): 0.5 mg/mlEthanol: 1 mg/ml
λmax
255, 376 nm
SMILES
Oc1cc(O)c2c(c1)oc(c1cc(O)c(O)c(O)c1)c(O)c2=O
InChi Code
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
InChi Key
IKMDFBPHZNJCSN-UHFFFAOYSA-N
Origin
Synthetic
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Myricetin is a flavonoid compound found in many fruits and vegetables, including red wine, that acts as a powerful antioxidant.1 Myricetin inhibits TBARS formation with an IC50 value of 6.34 and at 20 µM, blocks oxLDL uptake by U937-derived macrophages, reducing CD36 expression.2 Myricetin demonstrates potent chemopreventative potential by binding JAK1/STAT3 to inhibit the neoplastic transformation of murine JB6 P+ cells and inhibiting MEK1 kinase activity.3,4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Bennett, C.J., Caldwell, S.T., McPhail, D.B., et alPotential therapeutic antioxidants that combine the radical scavenging ability of myricetin and the lipophilic chain of vitamin E to effectively inhibit microsomal lipid peroxidation. Bioorg. Med. Chem. 12(9), 2079-2098 (2004).

    2. Lian, T.-W., Wang, L., Lo, Y.-H., et alFisetin, morin and myricetin attenuate CD36 expression and oxLDL uptake in U937-derived macrophages. Biochim. Biophys. Acta 1781(10), 601-609 (2008).

    3. Kumamoto, T., Fujii, M., and Hou, D.X. Myricetin directly targets JAK1 to inhibit cell transformation. Cancer Lett. 275(1), 17-26 (2009).

    4. Lee, K.W., Kang, N.J., Rogozin, E.A., et alMyricetin is a novel natural inhibitor of neoplastic cell transformation and MEK1. Carcinogenesis 28(9), 1918-1927 (2007).