Genkwanin

CAS No. 437-64-9

Genkwanin( Puddumetin )

Catalog No. M18551 CAS No. 437-64-9

Genkwanin exerts its anti-inflammatory effect mainly through the regulation of the miR-11/MKP-1/MAPK pathway.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 49 In Stock
50MG 79 In Stock
100MG 129 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Genkwanin
  • Note
    Research use only, not for human use.
  • Brief Description
    Genkwanin exerts its anti-inflammatory effect mainly through the regulation of the miR-11/MKP-1/MAPK pathway.
  • Description
    Genkwanin exerts its anti-inflammatory effect mainly through the regulation of the miR-11/MKP-1/MAPK pathway. Genkwanin is transported by both passive diffusion and multidrug resistance protein (MDR)-mediated efflux mechanisms.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Puddumetin
  • Pathway
    Tyrosine Kinase
  • Target
    Src
  • Recptor
    Others
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    437-64-9
  • Formula Weight
    284.26
  • Molecular Formula
    C16H12O5
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 5 mg/mL 17.59 mM; H2O : < 0.1 mg/mL
  • SMILES
    COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • A-770041

    A-770041 is selective and orally active Src-family Lck inhibitor, and the other Src family kinase involved in T-cell signaling.

  • Secretin, canine

    Secretin is an endocrine hormone that stimulates the secretion of bicarbonate-rich pancreatic fluids. Canine secretin can regulates gastric chief cell function and paracellular permeability in canine gastric monolayers by a Src kinase-dependent pathway.

  • DGY-06-116

    DGY-06-116 is an selective and irreversible covalent inhibitor of Src and FGFR1 with IC50 value of 3nM and 8340 nM, respectively.