Disclosed are novel pyrimido compounds that are selective inhibitors of both KDR an FGFR kinases and are selective against LCK. These compounds and their pharmaceutically acceptable salts are anti-proliferative agents useful in the treatment or control of solid tumors, in particular breast, colon, lung and prostate tumors. Also disclosed are pharmaceutical compositions containing these compounds and methods of treating cancer.

 
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< Implantable medical assembly

> Pyrazolopyrimidines as cyclin dependent kinase inhibitors

> Method for the selective preparation of 3-oxo-4-aza-5.alpha.-androstane compound

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