PHA-665752 |
| Catalog No.GC11733 |
Le PHA-665752 est un inhibiteur sélectif, compétitif pour l'ATP et À site actif de l'activité catalytique de la c-Met kinase (Ki = 4 nM; IC50 = 9 nM). PHA-665752 présente une sélectivité > 50 fois pour c-Met par rapport À un panel de diverses tyrosine et sérine-thréonine kinases. Le PHA-665752 induit l'apoptose et l'arrêt du cycle cellulaire, et présente une activité antitumorale cytoréductrice.
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Cas No.: 477575-56-7
Sample solution is provided at 25 µL, 10mM.
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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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