Synthesis of novel arylaminoquinazolinylurea derivatives and their antiproliferative activities against bladder cancer cell line.

Abstract

A novel series of arylurea and arylamide derivatives 1a-z, 2a-d having aminoquinazoline scaffold was designed and synthesized. Their in vitro antiproliferative activities against RT112 bladder cancer cell line and inhibitory activities against FGFR3 kinase were tested. Most compounds showed good antiproliferative activities against RT112 bladder cancer cell line, and arylurea compounds 1a-z were more potent than arylamide compounds 2a-d. Among them, eight compounds 1a, 1d-g, 1l, 1y, and 1z showed potent activities with GI50 values below submicromolar range. Especially, arylurea compounds 1d and 1g possessing 2,3-dimethyl and 3,4-dimethyl moieties exhibited superior or similar antiproliferative activity (GI50=8.8nM and 30.2nM, respectively) to AZD4547 (GI50=29.2nM) as a reference standard.

DOI: 10.1016/j.bmcl.2016.08.076

Cite this paper

@article{Kim2016SynthesisON, title={Synthesis of novel arylaminoquinazolinylurea derivatives and their antiproliferative activities against bladder cancer cell line.}, author={Jung Hun Kim and Yeonui Kwak and Chiman Song and Eun Joo Roh and Chang-Hyun Oh and So Ha Lee and Taebo Sim and Jung Hoon Choi and Kyung Ho Yoo}, journal={Bioorganic & medicinal chemistry letters}, year={2016}, volume={26 20}, pages={5082-5086} }