CP-609754

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

CP-609754 显示出对法呢基转移酶的选择性抑制。

CP-609754 shows selective inhibition of farnesyltransferase.(In Vitro):CP-609754 inhibits farnesylation (IC50?= 1.72 ng/mL) of mutant H-Ras in 3T3 H-ras (61L)-transfected cell lines. CP-609754 selectively inhibits farnesylation of both H- and K-Ras proteins in 3T3 transfectants. CP-609754 is competitive for the prenyl acceptor (H-Ras protein) and noncompetitive for the prenyl donor farnesyl PPI. CP-609754 interacts with the farnesyltransferase-farnesyl PPI complex and competes for the binding of the Ras protein.(In Vivo):CP-609754 has?in vivo?antitumor activity against 3T3 H-ras (61L) tumors. With twice daily oral dosing of CP-609754, tumor regression is achieved with a dose of 100 mg/kg; the ED50?for tumor growth inhibition is 28 mg/kg. With continuous i.p. infusion of CP-609754, tumor growth is inhibited by >50%, and tumor farnesyltransferase activity inhibited by >30% in mice in which the plasma concentration of CP-609754 is maintained above 118 ng/mL.

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OSI-754

Metabolic Enzyme/Protease

Transferase

Human Endogenous Metabolite

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1190094-64-4

479.96

C29H22ClN3O2

>98% (HPLC)

In Vitro:?DMSO : 100 mg/mL (208.35 mM)

N/A

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(-20℃)

With Ice Pack

≥ 2 years