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二氢吡咯并吡唑类转化生长因子-βⅠ型受体激酶结构域抑制剂的优化:发现一种口服生物可利用的转化生长因子-βⅠ型受体抑制剂作为抗肿瘤药物。

Optimization of a dihydropyrrolopyrazole series of transforming growth factor-beta type I receptor kinase domain inhibitors: discovery of an orally bioavailable transforming growth factor-beta receptor type I inhibitor as antitumor agent.

作者信息

Li Hong-Yu, McMillen William T, Heap Charles R, McCann Denis J, Yan Lei, Campbell Robert M, Mundla Sreenivasa R, King Chi-Hsin R, Dierks Elizabeth A, Anderson Bryan D, Britt Karen S, Huss Karen L, Voss Matthew D, Wang Yan, Clawson David K, Yingling Jonathan M, Sawyer J Scott

机构信息

Discovery Chemistry Research and Technology, Lead Optimization Biology, and Chemical Product Research and Development, Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.

出版信息

J Med Chem. 2008 Apr 10;51(7):2302-6. doi: 10.1021/jm701199p. Epub 2008 Mar 4.

Abstract

In our continuing effort to expand the SAR of the quinoline domain of dihydropyrrolopyrazole series, we have discovered compound 15d, which demonstrated the antitumor efficacy with oral bioavailability. This effort also demonstrated that the PK/PD in vivo target inhibition paradigm is an effective approach to assess potential for antitumor efficacy. The dihydropyrrolopyrazole inhibitor 15d (LY2109761) is representative of a novel series of antitumor agents.

摘要

在我们持续拓展二氢吡咯并吡唑系列喹啉结构域构效关系的工作中,我们发现了化合物15d,它展现出具有口服生物利用度的抗肿瘤功效。这项工作还表明,体内药代动力学/药效学靶点抑制模式是评估抗肿瘤功效潜力的有效方法。二氢吡咯并吡唑抑制剂15d(LY2109761)是一系列新型抗肿瘤药物的代表。

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