PHA-408

CAS No. 503555-55-3

PHA-408( PHA-767408 | PHA767408 | PHA 408 )

Catalog No. M14711 CAS No. 503555-55-3

A novel potent, highly selective, ATP-competitive IKK-2 inhibitor with IC50 of 40 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    PHA-408
  • Note
    Research use only, not for human use.
  • Brief Description
    A novel potent, highly selective, ATP-competitive IKK-2 inhibitor with IC50 of 40 nM.
  • Description
    A novel potent, highly selective, ATP-competitive IKK-2 inhibitor with IC50 of 40 nM, 350-fold selectivity over IKK-1; inhibits LPS-induces TNF-α producton in PBMCs and HWB with IC50 of 20-30 nM, prevents IL-1β-induced IκBα phosphorylation in RASFs while sparing the JNK and p38 MAPK pathways and has no effect on IKK-2 phosphorylation; demonstrates target-specific anti-inflammatory activities in in vivo model of airway inflammation.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    PHA-767408 | PHA767408 | PHA 408
  • Pathway
    Immunology/Inflammation
  • Target
    IκB kinase (IKK)
  • Recptor
    IκB kinase (IKK)
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    503555-55-3
  • Formula Weight
    560.03
  • Molecular Formula
    C29H27ClFN7O2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(C1=NN(C2=CC=C(F)C=C2)C3=C1CCC4=CC=C(NC(C5=C(Cl)C=NC(N6CCN(C)CC6)=C5)=O)C=C43)N
  • Chemical Name
    8-[[[5-Chloro-2-(4-methyl-1-piperazinyl)-4-pyridinyl]carbonyl]amino]-1-(4-fluorophenyl)-4,5-dihydro-1H-benz[g]indazole-3-carboxamide

Shipping & Storage Information

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

Reference

1. Mbalaviele G, et al. J Pharmacol Exp Ther. 2009 Apr;329(1):14-25. 2. Sommers CD, et al. J Pharmacol Exp Ther. 2009 Aug;330(2):377-88. 3. Xie J, et al. Bioorg Med Chem. 2011 Feb 1;19(3):1242-55.
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