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Bioorg Med Chem Lett ; 15(17): 3881-5, 2005 Sep 01.
Article in English | MEDLINE | ID: mdl-15993068

ABSTRACT

The inhibition of cyclin-dependent kinase 4 (Cdk4) causes cell cycle arrest and restores a checkpoint that is absent in the majority of tumor cells. Compounds that inhibit Cdk4 selectively are targeted for treating cancer. Appropriate substitution of 2-aminoquinazolines is demonstrated to produce high levels of selectivity for Cdk4 versus closely related serine-threonine kinases.


Subject(s)
Antineoplastic Agents/chemical synthesis , Cyclin-Dependent Kinases/antagonists & inhibitors , Proto-Oncogene Proteins/antagonists & inhibitors , Quinazolines/chemical synthesis , Antineoplastic Agents/pharmacology , Cyclin-Dependent Kinase 4 , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/pharmacology , Humans , Inhibitory Concentration 50 , Quinazolines/pharmacology , Structure-Activity Relationship
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