N-heteroaryl pyrazolopyrimidines as cyclin dependent kinase...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C544S281000, C514S263320, C514S252170, C514S183000, C514S081000, C514S110000, C514S234200, C514S252160, C514S151000, C514S008100, C514S009100, C514S027000, C514S167000, C514S015800, C514S221000, C514S245000, C424S649000, C424S094400

Reexamination Certificate

active

07470695

ABSTRACT:
In its many embodiments, the present invention provides a novel class of pyrazolo[1,5-a]pyrimidine compounds as inhibitors of cyclin dependent kinases, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the CDKs using such compounds or pharmaceutical compositions.

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