Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1367101 | Bioorganic & Medicinal Chemistry Letters | 2007 | 5 Pages |
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.
Graphical abstractA 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 target, VEGFR2, Tie2, and EphB4, have been successfully discovered.Figure optionsDownload full-size imageDownload as PowerPoint slide