PF-431396 supplier|PF431396|DC Chemicals

PF-431396 supplier|PF431396|DC Chemicals
DC Chemicals provides PF-431396, other names: PF 431396，PF431396, cas: 717906-29-1. In stock.

Contact: website: www.dcchemicals.com,
sales@dcchemicals.com,order@dcchemicals.com,info@dcchemicals.com,
Tel: +86-21-58447131;Fax:+86-21-61643271；

PF-431396 is dual focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (PYK2) inhibitor , PF-431396 has a Kd value of 445 nM for BRD4.

PF-431396, other names: PF 431396，PF431396, cas: 717906-29-1, Molecule formular: C22H21F3N6O3S, Molecule Weight: 506.5, Chemical name:  N-Methyl-N-[2-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)amino]-5-(trifluoromethyl)-4-pyrimidinyl]amino]methyl]phenyl]methanesulfonamide

PF-431396 is a potent and highly selective pyrimidine-based inhibitor of both Pyk2 and FAK, Consistent with the idea that the tyrosine phosphorylation of Pyk2 and FAK involves an initial autophosphorylation or transphosphorylation step, treating A20 cells with PF-431396 blocked anti-Ig-induced tyrosine phosphorylation of Pyk2 and FAK when the cells were stimulated in suspension when they were stimulated on ECM [3]. Nanomolar affinities were also determined for PF-431396 (Kd = 445 ± 42 nM) and for the PIM inhibitor (Kd = 565 ± 63 nM)  For the detailed information of PF-431396, the solubility of PF-431396 in water, the solubility of PF-431396 in DMSO, the solubility of PF-431396 in PBS buffer, the animal experiment (test) of  PF-431396, the cell expriment (test) of PF-431396, the in vivo, in vitro and clinical trial test of PF-431396, the EC50, IC50,and affinity,of PF-431396, Please contact DC Chemicals.