Pinocembrin chalcone

CAS No. 4197-97-1

Pinocembrin chalcone( 2',4',6'-Trihydroxychalcone | Pinocembrinchalcone )

Catalog No. M29214 CAS No. 4197-97-1

Pinocembrin chalcone is an inhibitor of tyrosinase with antimutagenic effects. Pinocembrin chalcone can be used in studies about the prevention of gastric ulcers.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 163 In Stock
10MG 242 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
    Pinocembrin chalcone
  • Note
    Research use only, not for human use.
  • Brief Description
    Pinocembrin chalcone is an inhibitor of tyrosinase with antimutagenic effects. Pinocembrin chalcone can be used in studies about the prevention of gastric ulcers.
  • Description
    Pinocembrin chalcone is an inhibitor of tyrosinase with antimutagenic effects. Pinocembrin chalcone can be used in studies about the prevention of gastric ulcers.(In Vitro):Pinocembrin chalcone exhibits antibacterial activity against the antibiotic-susceptible NG strain WHO V and Candida albicans with a MIC of 100 μg/mL.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    2',4',6'-Trihydroxychalcone | Pinocembrinchalcone
  • Pathway
    GPCR/G Protein
  • Target
    Calcium Channel
  • Recptor
    Calcium Channel
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    4197-97-1
  • Formula Weight
    256.257
  • Molecular Formula
    C15H12O4
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Oc1cc(O)c(C(=O)C=Cc2ccccc2)c(O)c1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Cav 2.2 blocker 1

    Cav 2.2 blocker 1 is an N-type calcium channel (Cav 2.2; IC50: 1 nM) blocker for the treatment of pain.

  • Oxodipine

    Oxodipine, a dihydropyridine-type calcium antagonist, inhibited KCl-induced aortic contraction in rabbits and reduced cardiac force in less potent rat ventricular test-paper contractions.

  • (S)-crizotinib

    (S)-crizotinib(IC50 of 72 nM), an effective MTH1 (NUDT1) inhibitor, is the (S)-enantiomer of crizotinib.