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PHA-665752

رقم الكتالوجGC11733

PHA-665752 هو مثبط انتقائي ، تنافسي لـ ATP ، ومثبط موقع نشط للنشاط التحفيزي لـ c-Met kinase (Ki = 4 نانومتر ؛ IC50 = 9 نانومتر)يعرض PHA-665752> انتقائية بمقدار 50 ضعفًا لـ c-Met مقارنة بلوحة متنوعة من كينازات التيروزين وسيرين ثريونينيستحث PHA-665752 موت الخلايا المبرمج وتوقف دورة الخلية ، ويعرض نشاطًا مضادًا للورم الخلوي

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PHA-665752 التركيب الكيميائي

Cas No.: 477575-56-7

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
109٫00
متوفر
10mg
90٫00
متوفر
50mg
287٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

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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