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 |
本文献已被 ScienceDirect 等数据库收录! |
|