Bioorganic & Medicinal Chemistry Letters 2006-08-15

Isothiazolopyrimidines and isoxazolopyrimidines as novel multi-targeted inhibitors of receptor tyrosine kinases.

Zhiqin Ji, Asma A Ahmed, Daniel H Albert, Jennifer J Bouska, Peter F Bousquet, George A Cunha, Keith B Glaser, Jun Guo, Junling Li, Patrick A Marcotte, Maria D Moskey, Lori J Pease, Kent D Stewart, Melinda Yates, Steven K Davidsen, Michael R Michaelides

文献索引：Bioorg. Med. Chem. Lett. , 4326, (2006)

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摘要

A series of isothiazolopyrimidines and isoxazolopyrimidines were synthesized and identified as potent KDR inhibitors. SAR studies led to isothiazolopyrimidine urea analogs that potently inhibit VEGFR tyrosine kinases (KDR enzymatic and cellular IC(50) values below 10 nM) as well as cKIT and TIE2. The selected compounds 8 and 13 display 56% and 48% oral bioavailability in mice, respectively.