IPI-549

CAS No. 1693758-51-8

IPI-549 ( IPI549;IPI 549 )

Catalog No. M12582 CAS No. 1693758-51-8

IPI-549 (IPI549) is apotent, highly selective, orally active inhibitor of PI3Kγ with IC50 of 16 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 38 In Stock
10MG 59 In Stock
25MG 104 In Stock
50MG 177 In Stock
100MG 321 In Stock
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Biological Information

  • Product Name
    IPI-549
  • Note
    Research use only, not for human use.
  • Brief Description
    IPI-549 (IPI549) is apotent, highly selective, orally active inhibitor of PI3Kγ with IC50 of 16 nM.
  • Description
    IPI-549 (IPI549) is apotent, highly selective, orally active inhibitor of PI3Kγ with IC50 of 16 nM, displays >100-fold selectivity over other lipid and protein kinases (PI3Kα IC50=3.2 uM, PI3Kβ IC50=3.5 uM, PI3Kδ IC50>8.4 uM); demonstrates excellent PI3Kγ potency (IC50=1.2 nM) and selectivity against other Class I PI3K isoforms (>146-fold) in cellular phospho-AKT assays, dose dependently inhibits PI3Kγ dependent bone marrow-derived macrophage (BMDM) migration; demonstrates favorable pharmacokinetic properties and robust inhibition of PI3K-γ mediated neutrophil migration in vivo.Solid Tumors Phase 1 Clinical
  • Synonyms
    IPI549;IPI 549
  • Pathway
    PI3K/Akt/mTOR signaling
  • Target
    PI3K
  • Recptor
    PI3K
  • Research Area
    Cancer
  • Indication
    Solid Tumors

Chemical Information

  • CAS Number
    1693758-51-8
  • Formula Weight
    528.56
  • Molecular Formula
    C30H24N8O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 15 mg/mL
  • SMILES
    O=C1N(C2=CC=CC=C2)C([C@@H](NC(C3=C(N=CC=C4)N4N=C3N)=O)C)=CC5=CC=CC(C#CC6=CN(C)N=C6)=C51
  • Chemical Name
    Pyrazolo[1,5-a]pyrimidine-3-carboxamide, 2-amino-N-[(1S)-1-[1,2-dihydro-8-[2-(1-methyl-1H-pyrazol-4-yl)ethynyl]-1-oxo-2-phenyl-3-isoquinolinyl]ethyl]-

Shipping & Storage Information

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

Reference

1. Evans CA, et al. ACS Med Chem Lett. 2016 Jul 22;7(9):862-7.
2. De Henau O, et al. Nature. 2016 Nov 17;539(7629):443-447.
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