AM-1430

• Description:

  AM-1430 is an efficient, highly selective and orally active small molecule inhibitor of PI3Kδ with an IC50 of 4.6 nM. AM-1430 exhibits IC50s for PI3Kα, PI3Kβ and PI3Kγ of 14.18, 2.2 and 3.22 μM, respectively. AM-1430 inhibits B cell proliferation and exhibits excellent in vivo activity in pAKT inhibition models and the hemoglobin (KLH) immune response model. AM-1430 can be used for the study of inflammation and autoimmune diseases[1].

• UNSPSC:

  12352005

• Target:

  PI3K

• Related Pathways:

  PI3K/Akt/mTOR

• Field of Research:

  Inflammation/Immunology

• Smiles:

  CNC(C1=C(C([C@@H](NC2=NC=NC(N)=C2C#N)C)=NC3=CC=CC(F)=C13)C4=NC=CC=C4)=O

• Molecular Formula:

  C23H19FN8O

• Molecular Weight:

  442.45

• References & Citations:

  [1]Gonzalez-Lopez de Turiso F, et al. Discovery and in Vivo Evaluation of the Potent and Selective PI3Kδ Inhibitors 2- ((1S) -1- ((6-Amino-5-cyano-4-pyrimidinyl) amino) ethyl) -6-fluoro-N-methyl-3- (2-pyridinyl) -4-quinolinecarboxamide (AM-0687) and 2- ((1S) -1- ((6-Amino-5-cyano-4-pyrimidinyl) amino) ethyl) -5-fluoro-N-methyl-3- (2-pyridinyl) -4-quinolinecarboxamide (AM-1430) . J Med Chem. 2016 Aug 11;59 (15) :7252-67.

• Shipping Conditions:

  Room temperature

• Scientific Category:

  Reference compound1

• Clinical Information:

  No Development Reported

• Isoform:

  PI3Kα; PI3Kβ; PI3Kγ; PI3Kδ

• CAS Number:

  [1975263-74-1]