Scutellarein

CAS No. 529-53-3

Scutellarein( Scutellarein | 4',5,6,7-Tetrahydroxyflavone )

Catalog No. M17533 CAS No. 529-53-3

Scutellarein reduces inflammatory responses by inhibiting Src kinase activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 54 In Stock
2MG 32 In Stock
5MG 48 In Stock
10MG 69 In Stock
25MG 111 In Stock
50MG 158 In Stock
100MG 235 In Stock
200MG 349 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Scutellarein
  • Note
    Research use only, not for human use.
  • Brief Description
    Scutellarein reduces inflammatory responses by inhibiting Src kinase activity.
  • Description
    Scutellarein is natural product. Scutellarein from Scutellaria barbata induces apoptosis of human colon cancer HCT116 cells through the ROS-mediated mitochondria-dependent pathway. Scutellarein Reduces Inflammatory Responses by Inhibiting Src Kinase Activity.
  • In Vitro
    ——
  • In Vivo
    Animal Model:HFD mice Dosage:50 mg/kg Administration:in diet, 16 weeks Result:Reduced lipid accumulation and levels of inflammatory factors in the liver.
  • Synonyms
    Scutellarein | 4',5,6,7-Tetrahydroxyflavone
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    GPR
  • Recptor
    Src
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    529-53-3
  • Formula Weight
    286.24
  • Molecular Formula
    C15H10O6
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 30 mg/mL; 104.81 mM
  • SMILES
    c1cc(ccc1c1cc(=O)c2c(c(c(cc2o1)O)O)O)O
  • Chemical Name
    5,6,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

Shipping & Storage Information

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

Reference

1. Sung NY, et al. Korean J Physiol Pharmacol. 2015 Sep;19(5):441-9.
molnova catalog
related products
  • GTPL5846

    6-OAU(GTPL5846; 6-n-octylaminouracil) is a surrogate agonist of GPR84; activates human GPR84 in the presence of Gqi5 chimera in HEK293 cells with an EC50 of 105 nM in the PI assay.

  • ML 145

    ML 145 is a selective and potent antagonist of human GPR35, with no significant activity against GPR35 in any of its immediate rodent homologs.

  • GPR120 Agonist 3

    GPR120-IN-1 is a selective agonist of Gpr120 ( logEC50: -7.62).