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Novel Mps1 kinase inhibitors: From purine to pyrrolopyrimidine and quinazoline leads
Authors:Matthew G. Bursavich  David Dastrup  Mark Shenderovich  Kraig M. Yager  Daniel M. Cimbora  Brandi Williams  D. Vijay Kumar
Affiliation:1. Medicinal Chemistry, Myrexis, Inc., 305 Chipeta Way, Salt Lake City, UT 84108, United States;2. In Vitro Pharmacology, Myrexis, Inc., 305 Chipeta Way, Salt Lake City, UT 84108, United States
Abstract:Mps1, also known as TTK, is a mitotic checkpoint protein kinase that has become a promising new target of cancer research. In an effort to improve the lead-likeness of our recent Mps1 purine lead compounds, a scaffold hopping exercise has been undertaken. Structure-based design, principles of conformational restriction, and subsequent scaffold hopping has led to novel pyrrolopyrimidine and quinazoline Mps1 inhibitors. These new single-digit nanomolar leads provide the basis for developing potent, novel Mps1 inhibitors with improved drug-like properties.
Keywords:Mps1  TTK  Protein kinase inhibitors  Scaffold hopping  Conformational restriction  Structure-based design  Cancer  Purines  Pyrrolopyrimidines  Quinazoline
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