| Literature DB >> 18651728 |
Nilantha Sirisoma1, Shailaja Kasibhatla, Azra Pervin, Hong Zhang, Songchun Jiang, J Adam Willardsen, Mark B Anderson, Vijay Baichwal, Gary G Mather, Kevin Jessing, Raouf Hussain, Khanh Hoang, Christopher M Pleiman, Ben Tseng, John Drewe, Sui Xiong Cai.
Abstract
Using a live cell, high-throughput caspase-3 activator assay, we have identified a novel series of 4-anilinoquinazolines as inducers of apoptosis. In this report, we discuss the discovery of 2-chloro-N-(4-methoxyphenyl)-N-methylquinazolin-4-amine, compound 2b (EP128265, MPI-0441138) as a highly active inducer of apoptosis (EC50 for caspase activation of 2 nM) and as a potent inhibitor of cell proliferation (GI50 of 2 nM) in T47D cells. Compound 2b inhibited tubulin polymerization, was effective in cells overexpressing ABC transporter Pgp-1, and was efficacious in the MX-1 human breast and PC-3 prostate cancer mouse models. In contrast to the SAR of 4-anilinoquinazolines as EGFR kinase inhibitors, the methyl group on the nitrogen linker was essential for the apoptosis-inducing activity of 4-anilinoquinazolines and substitution in the 6- and 7-positions of the quinazoline core structure decreased potency.Entities:
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Year: 2008 PMID: 18651728 DOI: 10.1021/jm8003653
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446