Article ID Journal Published Year Pages File Type
10592414 Bioorganic & Medicinal Chemistry Letters 2015 5 Pages PDF
Abstract
New carboxamide head group analogs of thieno[3,2-b]pyridine-based kinase inhibitor LCRF-0004 were designed and synthesized. Potent and selective inhibitors of RON enzyme over c-Met RTK were obtained.
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Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
Design and synthesis of close analogs of LCRF-0004, a potent and selective RON receptor tyrosine kinase inhibitor
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