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pubmed-article:18835709pubmed:abstractTextA novel series of pyrazolo[1,5-b]pyridazines have been synthesized and identified as cyclin dependant kinase inhibitors potentially useful for the treatment of solid tumors. Modification of the hinge-binding amine or the C(2)- and C(6)-substitutions on the pyrazolopyridazine core provided potent inhibitors of CDK4 and demonstrated enzyme selectivity against VEGFR-2 and GSK3beta.lld:pubmed
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pubmed-article:18835709pubmed:dateRevised2011-11-2lld:pubmed
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pubmed-article:18835709pubmed:articleTitleSynthesis and evaluation of pyrazolo[1,5-b]pyridazines as selective cyclin dependent kinase inhibitors.lld:pubmed
pubmed-article:18835709pubmed:affiliationDepartment of Oncology, GlaxoSmithKline, Research Triangle Park, NC 27709, USA. Kirk.L.Stevens@gsk.comlld:pubmed
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