PHA-665752 |
Catalog No.GC11733 |
PHA-665752 es un inhibidor selectivo, competitivo con ATP y del sitio activo de la actividad catalÍtica de la c-Met quinasa (Ki = 4 nM; IC50 = 9 nM). PHA-665752 exhibe una selectividad >50 veces mayor para c-Met en comparaciÓn con un panel de diversas tirosina y serina-treonina quinasas. PHA-665752 induce la apoptosis y la detenciÓn del ciclo celular y exhibe actividad antitumoral citorreductora.
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Cas No.: 477575-56-7
Sample solution is provided at 25 µL, 10mM.
PHA-665752 is a potent, ATP-competitive and specific c-Met receptor tyrosine kinase inhibitor with K(i) value of 4 nM and IC50 value of 9nM. PHA-665752 shows more than 50-fold selectivity for c-Met versus other serine-threonine and tyrosine kinases [1].
PHA-665752 has been demonstrated to inhibit hepatocyte growth factor (HGF) and c-Met-mediated cell proliferation, motility, invasion and morphology of pancreatic carcinoma cells BxPC-3, gastric carcinoma cells GTL-16 and lung cancer cells NCI-H441. Additionally, PHA-665752 inhibits the c-MET downstream mediators phosphorylation induced by HGF [1].
In vivo, PHA-665752 inhibits c-Met phosphorylation as well as tumor growth in both S114 and GTL-16 implanted xenograft athymic mice [1].
References:
[1] Christensen JG1, Schreck R, Burrows J, Kuruganti P, Chan E, Le P, Chen J, Wang X, Ruslim L, Blake R, Lipson KE, Ramphal J, Do S, Cui JJ,Cherrington JM, Mendel DB. A selective small molecule inhibitor of c-Met kinase inhibits c-Met-dependent phenotypes in vitro and exhibits cytoreductive antitumor activity in vivo. Cancer Res. 2003 Nov 1;63(21):7345-55.
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