Recent Progress in the Development of Small Molecule c-Met Inhibitors

Peng-Cheng      Lv; Yu-Shun      Yang; Zhong-Chang      Wang
doi:10.2174/1568026619666190712205353
Abstract

C-Met, also referred to as Hepatocyte Growth Factor Receptor (HGFR), is a heterodimeric receptor tyrosine kinase. It has been determined that c-Met gene mutations, overexpression, and amplification also occur in a variety of human tumor types, and these events are closely related to the aberrant activation of the HGF/c-Met signaling pathway. Meanwhile, high c-Met expression is closely associated with poor prognosis in cancer patients. The c-Met kinase has emerged as an attractive target for developing antitumor agents. In this review, we cover the recent advances on the small molecule c-Met inhibitors discovered from 2018 until now, with a main focus on the rational design, synthesis and structureactivity relationship analysis.
Keywords: c-Met, Tyrosine kinase, Small molecule inhibitors, Structure-activity relationship analysis, Anticancer agents, Drug development.
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Graphical Abstract

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DOI https://dx.doi.org/10.2174/1568026619666190712205353	Print ISSN 1568-0266
Publisher Name Bentham Science Publisher	Online ISSN 1873-4294
Current Topics in Medicinal Chemistry

Recent Progress in the Development of Small Molecule c-Met Inhibitors

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