| Literature DB >> 24900443 |
Pam Albaugh1, Yi Fan1, Yuan Mi1, Fangxian Sun1, Francisco Adrian1, Nanxin Li1, Yong Jia1, Yelena Sarkisova1, Andreas Kreusch1, Tami Hood1, Min Lu1, Guoxun Liu1, Shenlin Huang1, Zuosheng Liu1, Jon Loren1, Tove Tuntland1, Donald S Karanewsky1, H Martin Seidel1, Valentina Molteni1.
Abstract
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.Entities:
Keywords: GNF-5837; NGF; TRK; neurotrophins; oxindole; tropomyosin receptor kinase
Year: 2012 PMID: 24900443 PMCID: PMC4025649 DOI: 10.1021/ml200261d
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345