Discovery of multi-target receptor tyrosine kinase inhibitors as novel anti-angiogenesis agents

نویسندگان

  • Jinfeng Wang
  • Lin Zhang
  • Xiaoyan Pan
  • Bingling Dai
  • Ying Sun
  • Chuansheng Li
  • Jie Zhang
چکیده

Recently, we have identified a biphenyl-aryl urea incorporated with salicylaldoxime (BPS-7) as an anti-angiogenesis agent. Herein, we disclosed a series of novel anti-angiogenesis agents with BPS-7 as lead compound through combining diarylureas with N-pyridin-2-ylcyclopropane carboxamide. Several title compounds exhibited simultaneous inhibition effects against three pro-angiogenic RTKs (VEGFR-2, TIE-2 and EphB4). Some of them displayed potent anti-proliferative activity against human vascular endothelial cell (EA.hy926). In particular, two potent compounds (CDAU-1 and CDAU-2) could be considered as promising anti-angiogenesis agents with triplet inhibition profile. The biological evaluation and molecular docking results indicate that N-pyridin-2-ylcyclopropane carboxamide could serve as a hinge-binding group (HBG) for the discovery of multi-target anti-angiogenesis agents. CDAU-2 also exhibited promising anti-angiogenic potency in a tissue model for angiogenesis.

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عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2017