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Yao Xue Xue Bao ; 48(10): 1579-84, 2013 Oct.
Artigo em Chinês | MEDLINE | ID: mdl-24417085

RESUMO

A series of phthalazine ketone compounds were synthesized and the structures were confirmed by H NMR and HR-MS spectrum. All target compounds were obtained through 7 steps, including selective reduction, nitration, bromination, ring enlargement, reduction, Knoevenagel and acylated reaction. The compounds were evaluated for their immunosuppressive effects of T-cell proliferation and inhibitory activity of IMPDH type II in vitro, as well as their structure-activity relationship were assessed. Several compounds exhibited strong immunosuppressive properties, especially compounds 7f and 7h, with IC50 values of 0.093 micromol x L(-1) and 0.14 micromol x L(-1) respectively, which were superior to mycophenolic acid. The information obtained from the studies may be useful for further research on the immunosuppressive agents.


Assuntos
Proliferação de Células/efeitos dos fármacos , Imunossupressores/síntese química , Ftalazinas/síntese química , Animais , Feminino , IMP Desidrogenase/metabolismo , Imunossupressores/química , Imunossupressores/farmacologia , Concentração Inibidora 50 , Camundongos , Camundongos Endogâmicos BALB C , Ftalazinas/química , Ftalazinas/farmacologia , Baço/citologia , Relação Estrutura-Atividade , Linfócitos T/efeitos dos fármacos
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