Katacine

CAS No. 135151-34-7

Katacine( —— )

Catalog No. M17252 CAS No. 135151-34-7

Katacine inhibits of oxygen consumption and suppresses the speed of electrons transfer from oxidation substrates via respiratory chain of mitochondria to molecular oxygen.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 122 In Stock
5MG 236 In Stock
10MG 433 In Stock
25MG 708 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
    Katacine
  • Note
    Research use only, not for human use.
  • Brief Description
    Katacine inhibits of oxygen consumption and suppresses the speed of electrons transfer from oxidation substrates via respiratory chain of mitochondria to molecular oxygen.
  • Description
    Katacine inhibits of oxygen consumption and suppresses the speed of electrons transfer from oxidation substrates via respiratory chain of mitochondria to molecular oxygen.Katacine is a mixture of polymers of A-type proanthocyanidins at various stages of polymerisation , from Polygonum coriarium of the Polygonaceae family. Katacine is an antihypoxic.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    c-Kit
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    135151-34-7
  • Formula Weight
    ——
  • Molecular Formula
    (C15H13O7)-[C15H12O7]n-(C15H13O7)
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • ISCK03

    A specific c-Kit inhibitor that inhibits c-kit phosphorylation in vitro and SCF-induced c-kit phosphorylation in human melanoma cells.

  • INCB024360 analogue

    IDO-IN-2 is an effective IDO1 inhibitor(IC50=10 nM).

  • KI8751

    Ki8751 is a potent and selective inhibitor of VEGFR2 with IC50 of 0.9 nM.