Design and synthesis of 3-(4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridin-2-yl)-1H-quinolin-2-ones as VEGFR-2 kinase inhibitors

  • Han, Sun-Young; 
  • Choi, Jie Won; 
  • Yang, Jeon; 
  • Chae, Chong Hack; 
  • Lee, Jongkook; 
  • 외 5명
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초록

A series of 3-(4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridin-2-yl)-1H-quinolin-2-ones have been identified as a new class of VEGFR-2 kinase inhibitors. A variety of (4,5,6,7-tetrahydro-imidazo[5,4-c]pyridin-2-yl)-acetic acid ethyl esters were synthesized, and their VEGFR-2 inhibitory activity was evaluated. Described herein are the preparation of the series and the effects of the compounds on VEGFR-2 kinase activity. (C) 2012 Elsevier Ltd. All rights reserved.

키워드

Cancer; VEGFR-2; KDR kinase; Imidazo[4,5-c]pyridine; Quinolin-2-one; ENDOTHELIAL GROWTH-FACTOR; ORAL MULTIKINASE INHIBITOR; CANCER-THERAPY; ANGIOGENESIS; BEVACIZUMAB; PHARMACOKINETICS; NAPHTHAMIDES; RECEPTORS; SUNITINIB; ANTIBODY
제목
Design and synthesis of 3-(4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridin-2-yl)-1H-quinolin-2-ones as VEGFR-2 kinase inhibitors
저자
Han, Sun-Young; Choi, Jie Won; Yang, Jeon; Chae, Chong Hack; Lee, Jongkook; Jung, Heejung; Lee, Kwangho; Ha, Jae Du; Kim, Hyoung Rae; Cho, Sung Yun
DOI
10.1016/j.bmcl.2012.02.073
발행일
2012-04-15
유형
Article
저널명
Bioorganic & Medicinal Chemistry Letters
권
22
호
8
페이지
2837 ~ 2842