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J Med Chem ; 49(24): 7247-51, 2006 Nov 30.
Article in English | MEDLINE | ID: mdl-17125279

ABSTRACT

The optimization of a series of 5-phenylacetyl 1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole derivatives toward the inhibition of Aurora kinases led to the identification of compound 9d. This is a potent inhibitor of Aurora kinases that also shows low nanomolar potency against additional anticancer kinase targets. Based on its high antiproliferative activity on different cancer cell lines, favorable chemico-physical and pharmacokinetic properties, and high efficacy in in vivo tumor models, compound 9d was ultimately selected for further development.


Subject(s)
Antineoplastic Agents/chemical synthesis , Protein Serine-Threonine Kinases/antagonists & inhibitors , Pyrazoles/chemical synthesis , Pyrroles/chemical synthesis , Animals , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Aurora Kinases , Cell Line, Tumor , Drug Screening Assays, Antitumor , Male , Mice , Models, Molecular , Pyrazoles/pharmacokinetics , Pyrazoles/pharmacology , Pyrroles/pharmacokinetics , Pyrroles/pharmacology , Solubility , Structure-Activity Relationship
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