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Cited 37 time in webofscience Cited 38 time in scopus
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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

Authors
Han, Sun-YoungChoi, Jie WonYang, JeonChae, Chong HackLee, JongkookJung, HeejungLee, KwanghoHa, Jae DuKim, Hyoung RaeCho, Sung Yun
Issue Date
Apr-2012
Publisher
Pergamon Press Ltd.
Keywords
Cancer; VEGFR-2; KDR kinase; Imidazo[4,5-c]pyridine; Quinolin-2-one
Citation
Bioorganic & Medicinal Chemistry Letters, v.22, no.8, pp 2837 - 2842
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
Bioorganic & Medicinal Chemistry Letters
Volume
22
Number
8
Start Page
2837
End Page
2842
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/22223
DOI
10.1016/j.bmcl.2012.02.073
ISSN
0960-894X
1464-3405
Abstract
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.
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