PKCβ inhibitor 1?

CAS No. 257879-35-9

PKCβ inhibitor 1?( KUN79359 )

Catalog No. M21636 CAS No. 257879-35-9

PKCβ inhibitor 1(KUN79359) is a potent selective and ATP-competitive inhibitor of PKC isozymes(IC50s of 21 and 5 nM for human PKCβ1 and PKCβ2 respectively).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 318 Get Quote
5MG 554 Get Quote
10MG 789 Get Quote
25MG 1188 Get Quote
50MG 1611 Get Quote
100MG 2151 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    PKCβ inhibitor 1?
  • Note
    Research use only, not for human use.
  • Brief Description
    PKCβ inhibitor 1(KUN79359) is a potent selective and ATP-competitive inhibitor of PKC isozymes(IC50s of 21 and 5 nM for human PKCβ1 and PKCβ2 respectively).
  • Description
    PKCβ inhibitor 1(KUN79359) is a potent selective and ATP-competitive inhibitor of PKC isozymes(IC50s of 21 and 5 nM for human PKCβ1 and PKCβ2 respectively).
  • In Vitro
    PKCβ inhibitor 1 (0-30 μM; 48 hours) suppresses tumor cell proliferation in a time- and dose-dependent manner.PKCβ inhibitor 1 (14 μM; 2-48 hours) induces apoptosis in 2F7 cells.PKCβ inhibitor 1 (15 μM; 2-48 hours) inhibits cell cycle progression in 2F7 and BCBL-1 cells.PKCβ (15 or 14 μM, respectively; 2-48 hours) inhibitor 1 reduces the expression of phospho-PKCβ in BCBL-1 and 2F7 cells.PKCβ inhibitor 1(0-48 hours) suppresses GSK3β, mTOR, and S6 phosphorylation. Cell Proliferation Assay Cell Line:2F7, BCBL-1 cells Concentration:0, 5, 10, 20, and 30 μMIncubation Time:48 hours Result:A dose-dependent reduction in viability of the 2F7 and BCBL-1 cells starting at 5 μM and increasing with elevated inhibitor concentration. Apoptosis Analysis Cell Line:2F7 cells Concentration:14 μM Incubation Time:2-48 hours Result:Apoptotic induction in 2.1% of the 2F7 cells above background after 2 hours of treatment, increasing through 48 hours of treatment.Cell Cycle AnalysisCell Line:BCBL-1 Cells Concentration:15 μM (the IC50)Incubation Time:2-48 hours Result:Inhibits cell cycle progression in 2F7 and BCBL-1 cells.Western Blot Analysis Cell Line:BCBL-1 and 2F7 cell lines Concentration:15 or 14 μM (at the IC50 respectively)Incubation Time:2-48 hours Result:The expression of phospho-PKCβ in BCBL-1 and 2F7 cells reduced.
  • In Vivo
    ——
  • Synonyms
    KUN79359
  • Pathway
    Angiogenesis
  • Target
    PKC
  • Recptor
    PKCβ
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    257879-35-9
  • Formula Weight
    411.5
  • Molecular Formula
    C24H21N5O2?
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 250 mg/mL (607.59 mM)
  • SMILES
    ——
  • Chemical Name
    3-[1-(3-Imidazol-1-yl-propyl)-1H-indol-3-yl]-4-phenylamino-pyrrole-25-dione

Shipping & Storage Information

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

Reference

1.Saba N S Levy L S . Protein Kinase C-Beta Inhibition Induces Apoptosis and Inhibits Cell Cycle Progression in Acquired Immunodeficiency Syndrome–Related Non-Hodgkin Lymphoma Cells[J]. Journal of Investigative Medicine 2012 60(1):29-.
molnova catalog
related products
  • CGP-53353

    CGP-53353 (DAPH-7) is a selective inhibitor of PKCβII with IC50 of 0.41 uM, shows weak activity on PKCβI with IC50 of 3.8 uM.

  • UCN-01

    UCN-01 (7-Hydroxystaurosporine;NSC 638850) is a synthetic derivative of staurosporine that has antiproliferative activity against several in vitro and in vivo cancer models.

  • PKC-IN-7

    PKC-IN-7 is a potent, selective, reversible, ATP-competitive PKCα/β inhibitor with IC50 of 4.7/3.3 nM.