Homobutein

CAS No. 34000-39-0

Homobutein( 2',4,4'-Trihydroxy-3-methoxychalcone | 3-O-Methylbutein )

Catalog No. M29306 CAS No. 34000-39-0

Homobutein is a dual inhibitor of HDACs and NF-κB with IC50s of 190 and 38 μM. Homobutein is an iron chelator with anticancer, anti-inflammatory, antiparasite, and antioxidation activities.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 188 In Stock
10MG 282 In Stock
25MG 489 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Homobutein
  • Note
    Research use only, not for human use.
  • Brief Description
    Homobutein is a dual inhibitor of HDACs and NF-κB with IC50s of 190 and 38 μM. Homobutein is an iron chelator with anticancer, anti-inflammatory, antiparasite, and antioxidation activities.
  • Description
    Homobutein is a dual inhibitor of HDACs and NF-κB with IC50s of 190 and 38 μM. Homobutein is an iron chelator with anticancer, anti-inflammatory, antiparasite, and antioxidation activities.(In Vitro):Homobutein (1 μg/mL) inhibits the growth of Toxoplasma gondii by 19.48% with IC50s of 15.0 and 16.1 μM for W2 and D6 strains of P. falciparum. Homobutein (20 - 40 μM) inhibits the viability and TNFα-induced NF-κB activity of K562 cells.
  • In Vitro
    Homobutein (compound 15) (20, 24, 28, 32, 40 μM; 2 h) inhibits the viability of K562 cells.Homobutein (2 h) inhibits TNFα-induced NF-κB activity in K562 cells.Homobutein (1 μg/mL; 72 h) inhibits the growth of Toxoplasma gondii by 19.48%.Homobutein (24 h) againsts W2 and D6 strains of P.falciparum with IC50s of 15.0 and 16.1 μM, respectively.Cell Viability Assay Cell Line:K562 cells Concentration:20, 24, 28, 32, 40 μM Incubation Time:2 h Result:Showed inhibition of viability in K562 cells.Cell Viability AssayCell Line:Toxoplasma gondii RH-2F strain Concentration:1 μg/mL Incubation Time:72 h Result:Surpressed 19.48% of the Toxoplasma gondii.
  • In Vivo
    ——
  • Synonyms
    2',4,4'-Trihydroxy-3-methoxychalcone | 3-O-Methylbutein
  • Pathway
    Others
  • Target
    Antioxidant
  • Recptor
    Antioxidant
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    34000-39-0
  • Formula Weight
    286.28
  • Molecular Formula
    C16H14O5
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C(=C/C(=O)C1=C(O)C=C(O)C=C1)\C2=CC(OC)=C(O)C=C2
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • DIM-C-pPhOH

    Nur77 (NR4A1) antagonist. Inhibits TGF-β induced cell migration of breast cancer cell lines. Promotes ROS/endoplasmic reticulum stress and proapoptotic pathways in pancreatic cancer cell lines.

  • BMY 7378 dihydrochlo...

    BMY-7378, α1D-adrenergic receptor antagonist, is a weak partial agonist/antagonist of 5-HT1A receptor.

  • Genipin 1-β-D-gentio...

    Genipin 1-β-D-gentiobioside (Genipin 1-gentiobioside) is one of the most abundant and bioactive iridoid glycosides in?Gardenia jasminoides?Ellis, which possesses hepatoprotective, anti-inflammatory, antioxidant, and antithrombotic activities.