Discovery of a novel and potent series of thieno[3,2-b]pyridine-based inhibitors of c-Met and VEGFR2 tyrosine kinases

被引:68
|
作者
Claridge, Stephen [1 ]
Raeppel, Franck [1 ]
Granger, Marie-Claude [1 ]
Bernstein, Naomy [1 ]
Saavedra, Oscar [1 ]
Zhan, Lijie [1 ]
Llewellyn, David [1 ]
Wahhab, Amal [1 ]
Deziel, Robert [1 ]
Rahil, Jubrail [3 ]
Beaulieu, Normand [2 ]
Nguyen, Hannah [2 ]
Dupont, Isabelle [2 ]
Barsalou, Annie [2 ]
Beaulieu, Carole [2 ]
Chute, Ian [2 ]
Gravel, Serge [2 ]
Robert, Marie-France [2 ]
Lefebvre, Sylvain [2 ]
Dubay, Marja [2 ]
Pascal, Roussen [4 ]
Gillespie, Jeff [4 ]
Jin, Zhiyun [4 ]
Wang, James [4 ]
Besterman, Jeffrey M. [2 ]
MacLeod, A. Robert [2 ]
Vaisburg, Arkadii [1 ]
机构
[1] MethylGene Inc, Dept Med Chem, Montreal, PQ H4S 2A1, Canada
[2] MethylGene Inc, Dept Cell Biol & Pharmacol, Montreal, PQ H4S 2A1, Canada
[3] MethylGene Inc, Dept Lead Discovery, Montreal, PQ H4S 2A1, Canada
[4] MethylGene Inc, Dept PK Analyt Chem, Montreal, PQ H4S 2A1, Canada
关键词
c-Met; VEGFR2; kinase; thieno[3,2-b]pyridine; cancer;
D O I
10.1016/j.bmcl.2008.04.009
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of thieno[3,2-b]pyridine-based inhibitors of c-Met and VEGFR2 tyrosine kinases is described. The compounds demonstrated potency with IC50 values in the low nanomolar range in vitro while the lead compound also showed in vivo activity against various human tumor xenograft models in mice. Further exploration of this class of compounds is underway. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2793 / 2798
页数:6
相关论文
共 39 条
  • [31] Discovery of a novel 6,7-disubstituted-4-(2-fluorophenoxy)quinolines bearing 1,2,3-triazole-4-carboxamide moiety as potent c-Met kinase inhibitors
    Liu, Mingmei
    Hou, Yunlei
    Yin, Weile
    Zhou, Shunguang
    Qian, Ping
    Guo, Zhuang
    Xu, Liying
    Zhao, Yangfang
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2016, 119 : 96 - 108
  • [32] Structure-based discovery of novel 4-(2-fluorophenoxy)quinoline derivatives as c-Met inhibitors using isocyanide-involved multicomponent reactions
    Nan, Xiang
    Li, Hui-Jing
    Fang, Sen-Biao
    Li, Qin-Ying
    Wu, Yan-Chao
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2020, 193
  • [33] Discovery of Novel Pyrrolo[2,3-b]pyridine-Based CSF-1R Inhibitors with Demonstrated Efficacy against Patient-Derived Colorectal Cancer Organoids
    He, Jinting
    Gao, Wen
    Dong, Rongrong
    Lv, Yingshan
    Zhang, Qiang
    Li, Lin
    Xie, Xiaolong
    Lv, Qi
    Hu, Lihong
    Wang, Junwei
    JOURNAL OF MEDICINAL CHEMISTRY, 2025, 68 (05) : 5655 - 5674
  • [34] Synthesis, fluorescence properties of novel thiazolo[3,2-b][1,2,4]triazol derivatives as potent SHP2 inhibitors and its uses in sensing for Fe3+and cell imaging
    Yan, Xue
    Zhang, Chun
    Gao, Li-Xin
    Cao, Zi-Tong
    Gan, Su-Ya
    Li, Jia
    Xiang, Da-Jun
    Zhou, Yu-Bo
    Wang, Wen-Long
    JOURNAL OF MOLECULAR STRUCTURE, 2025, 1324
  • [35] Pyrrolo[3,2-b]quinoxaline Derivatives as Types I1/2 and II Eph Tyrosine Kinase Inhibitors: Structure-Based Design, Synthesis, and in Vivo Validation
    Unzue, Andrea
    Dong, Jing
    Lafleur, Karine
    Zhao, Hongtao
    Frugier, Emilie
    Caflisch, Amedeo
    Nevado, Cristina
    JOURNAL OF MEDICINAL CHEMISTRY, 2014, 57 (15) : 6834 - 6844
  • [36] Discovery of novel pyrazole based Urea/Thiourea derivatives as multiple targeting VEGFR-2, EGFRWT, EGFRT790M tyrosine kinases and COX-2 Inhibitors, with anti-cancer and anti-inflammatory activities
    Fadaly, Wael A. A.
    Nemr, Mohamed T. M.
    Kahk, Nesma M.
    BIOORGANIC CHEMISTRY, 2024, 147
  • [37] Discovery of 6-(difluoro(6-(4-fluorophenyl)-[1,2,4]triazolo[4,3-b] [1,2,4]triazin-3-yl)methyl)quinoline as a highly potent and selective c-Met inhibitor
    Zhan, Zhengsheng
    Peng, Xia
    Liu, Qiufeng
    Chen, Fang
    Ji, Yinchun
    Yao, Shanyan
    Xi, Yong
    Lin, Yipeng
    Chen, Tiantian
    Xu, Yechun
    Ai, Jing
    Geng, Meiyu
    Duan, Wenhu
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2016, 116 : 239 - 251
  • [38] Design and synthesis of novel DFG-out RAF/vascular endothelial growth factor receptor 2 (VEGFR2) inhibitors: 3. Evaluation of 5-amino-linked thiazolo[5,4-d]pyrimidine and thiazolo[5,4-b]pyridine derivatives
    Hirose, Masaaki
    Okaniwa, Masanori
    Miyazaki, Tohru
    Imada, Takashi
    Ohashi, Tomohiro
    Tanaka, Yuta
    Arita, Takeo
    Yabuki, Masato
    Kawamoto, Tomohiro
    Tsutsumi, Shunichirou
    Sumita, Akihiko
    Takagi, Terufumi
    Sang, Bi-Ching
    Yano, Jason
    Aertgeerts, Kathleen
    Yoshida, Sei
    Ishikawa, Tomoyasu
    BIOORGANIC & MEDICINAL CHEMISTRY, 2012, 20 (18) : 5600 - 5615
  • [39] Identification of 3-substituted-6-(1-(1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)ethyl)quinoline derivatives as highly potent and selective mesenchymal-epithelial transition factor (c-Met) inhibitors via metabolite profiling-based structural optimization
    Zhao, Fei
    Zhang, Le-Duo
    Hao, Yu
    Chen, Na
    Bai, Rui
    Wang, Yu-Ji
    Zhang, Chun-Chun
    Li, Gong-Sheng
    Hao, Li-Jun
    Shi, Chen
    Zhang, Jing
    Mao, Yu
    Fan, Yi
    Xia, Guang-Xin
    Yu, Jian-Xin
    Liu, Yan-Jun
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 134 : 147 - 158