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J Med Chem ; 58(20): 8309-13, 2015 Oct 22.
Article in English | MEDLINE | ID: mdl-26356364

ABSTRACT

As part of a program to develop a small molecule inhibitor of LIMK, a series of aminothiazole inhibitors were discovered by high throughput screening. Scaffold hopping and subsequent SAR directed development led to a series of low nanomolar inhibitors of LIMK1 and LIMK2 that also inhibited the direct biomarker p-cofilin in cells and inhibited the invasion of MDA MB-231-luc cells in a matrigel inverse invasion assay.


Subject(s)
Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/pharmacology , Lim Kinases/antagonists & inhibitors , Thiazoles/chemical synthesis , Thiazoles/pharmacology , Actin Depolymerizing Factors/metabolism , Animals , Biotransformation , Drug Design , High-Throughput Screening Assays , Humans , Microsomes, Liver/metabolism , Neoplasm Invasiveness , Structure-Activity Relationship
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