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Discovery of GNF-5837, a Selective TRK Inhibitor with Efficacy in Rodent Cancer Tumor Models

  作者 ALBAUGH PAM; FAN YI; MI YUAN; SUN FANGXIAN; ADRIAN FRANCISCO; LI NANXIN; JIA YONG; SARKISOVA YELENA; KREUSCH ANDREAS; HOOD TAMI; LU MIN; LIU GUOXUN; HUANG SHENLIN; LIU ZUOSHENG; LOREN JON; TUNTLAND TOVE; KARANEWSKY DONALD S; SEIDEL H MARTIN; MOLTENI VALENTINA  
  选自 期刊  ACS Medicinal Chemistry Letters;  卷期  2012年3-2;  页码  140-145  
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[摘要]Neurotrophins and their receptors (TRKs) play key roles in the development of the nervous system and the maintenance of the neural network. Accumulating evidence points to their role in malignant transformations, chemotaxis, metastasis, and survival signaling and may contribute to the pathogenesis of a variety of tumors of both neural and non-neural origin. By screening the GNF kinase collection, a series of novel oxindole inhibitors of TRKs were identified. Optimization led to the identification of GNF-5837 (22), a potent, selective, and orally bioavailable pan-TRK inhibitor that inhibited tumor growth in a mouse xenograft model derived from RIE cells expressing both TRKA and NGF. The properties of 22 make it a good tool for the elucidation of TRK biology in cancer and other nononcology indications.

 
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