Home - Products - Others - Other Targets - 5,7,3-Trihydroxy-6,4,5-trimethoxyflavone

5,7,3-Trihydroxy-6,4,5-trimethoxyflavone

CAS No. 78417-26-2

5,7,3-Trihydroxy-6,4,5-trimethoxyflavone( —— )

Catalog No. M24784 CAS No. 78417-26-2

5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone is a natural product from Artemisia argyi.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 265 In Stock
5MG 235 In Stock
10MG 364 In Stock
25MG 645 In Stock
50MG 923 In Stock
100MG 1237 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    5,7,3-Trihydroxy-6,4,5-trimethoxyflavone
  • Note
    Research use only, not for human use.
  • Brief Description
    5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone is a natural product from Artemisia argyi.
  • Description
    5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone is a natural product from Artemisia argyi.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    78417-26-2
  • Formula Weight
    360.3
  • Molecular Formula
    C18H16O8
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mM
  • SMILES
    COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Further characterization of foliar flavonoids in Crossostephium chinense and their geographic variation.Nat Prod Commun. 2014 Feb;9(2):163-4.
molnova catalog
related products
  • Schizotenuin A

    The herbs of Nepeta cataria.

  • Moschamine

    Moschamine is a very potent compound that is able to inhibit COX-I by 58% and COX-II by 54%, at the concentration of 0.1 μmol L⁻1, it may suppress cAMP formation via binding to 5-HT1 receptors in the cells. Moschamine exerts antitumour effects on HeLa, MCF7 and A431 cells.

  • (E)-SI-2

    (E)-SI-2 is a potent small-molecule inhibitor of steroid receptor coactivator-3 (SRC-3 or AIB1) that can selectively inhibit the intrinsic transcriptional activities of SRC-3, also inhibits SRC-1 and SRC-2.