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Yao Xue Xue Bao ; (12): 1579-1584, 2013.
Artigo em Chinês | WPRIM | ID: wpr-298041

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
Animais , Feminino , Camundongos , Proliferação de Células , IMP Desidrogenase , Metabolismo , Imunossupressores , Química , Farmacologia , Concentração Inibidora 50 , Camundongos Endogâmicos BALB C , Ftalazinas , Química , Farmacologia , Baço , Biologia Celular , Relação Estrutura-Atividade , Linfócitos T
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