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Design and effective synthesis of novel templates, 3, 7-diphenyl-4-amino-thieno and furo-[3, 2-c] pyridines as protein kinase inhibitors and in vitro evaluation targeting …

…, EN Nartey, KE Hightower, L Kane-Carson

文献索引:Miyazaki, Yasushi; Nakano, Masato; Sato, Hideyuki; Truesdale, Anne T.; Stuart, J. Darren; Nartey, Eldridge N.; Hightower, Kendra E.; Kane-Carson, Laurie Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 1 p. 250 - 254

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被引用次数: 44

摘要

A novel class of 3, 7-diphenyl-4-amino-thieno and furo [3, 2-c] pyridine has been designed based on pharmacophore models of ATP competitive kinase inhibitors. Versatile synthetic methods via double Suzuki coupling to explore SAR have been established and potent inhibitors against angiogenetic targets, VEGFR2, Tie-2, and EphB4, have been successfully discovered.

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