Novel methyl indolinone-6-carboxylates containing an indole moiety as angiokinase inhibitors

  • Eur J Med Chem. 2017 Oct 20:139:492-502. doi: 10.1016/j.ejmech.2017.08.031.
Mingze Qin  1 Ye Tian  1 Xiaoqing Sun  1 Simiao Yu  1 Juanjuan Xia  1 Ping Gong  1 Haotian Zhang  2 Yanfang Zhao  3
Affiliations
  • 1. Key Laboratory of Structure-Based Drug Design and Discovery (Shenyang Pharmaceutical University), Ministry of Education, 103 Wenhua Road, Shenyang 110016, PR China.
  • 2. Department of Pharmacology, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, PR China. Electronic address: [email protected].
  • 3. Key Laboratory of Structure-Based Drug Design and Discovery (Shenyang Pharmaceutical University), Ministry of Education, 103 Wenhua Road, Shenyang 110016, PR China. Electronic address: [email protected].
Abstract

A novel series of methyl indolinone-6-carboxylates bearing an indole moiety were identified as potent angiokinase inhibitors. The most active compound, A8, potently targeted the kinase activities of vascular endothelial growth factor receptors 2 and 3, and platelet-derived growth factor receptors α and β, with IC50 values in the nanomolar range. In addition, A8 effectively suppressed the proliferation of human umbilical vein endothelial cells, and HT-29 and MCF-7 Cancer cells, by inducing Apoptosis. Compound A8 is thus a promising candidate for further investigation.

Keywords
Angiokinase inhibitors; Antitumour activity; Methyl indolinone-6-carboxylates; Ring-fused strategy.