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Molecules ; 17(3): 2351-66, 2012 Feb 24.
Artigo em Inglês | MEDLINE | ID: mdl-22367029

RESUMO

A series of N-3-substituted 7-aminopyrido[2,3-d]pyrimidin-6-carbonitrile derivatives was readily synthesized and their anti-proliferative activities on five types of tumor cells were evaluated through a cell-based phenotypic screening approach. Compound 3k was found to be potent on human colon cancer SW620 cells with an IC(50) value of 12.5 mM. Structural optimization of compound 3k led to compound 4a with improved anti-proliferative potency on SW620 cells with an IC(50) value of 6.9 mM. Further cell-cycle analyses suggested that compound 4a induced apoptosis of SW620 cells in a concentration-dependent manner.


Assuntos
Antineoplásicos/síntese química , Nitrilas/síntese química , Pirimidinas/síntese química , Antineoplásicos/farmacologia , Ciclo Celular/efeitos dos fármacos , Linhagem Celular Tumoral , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Concentração Inibidora 50 , Nitrilas/farmacologia , Pirimidinas/farmacologia , Relação Estrutura-Atividade
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