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Acta Pharmaceutica Sinica ; (12): 263-267, 2010.
Artigo em Chinês | WPRIM | ID: wpr-250632

RESUMO

A series of novel quinolinone acid-containing compounds were designed and synthesized. Their structures were confirmed with 1H NMR and MS. The target compounds were tested for anti-HIV-1 integrase activities in vitro with enzyme linked immunosorbent assay (ELISA). The result showed that D-2, D-4 and D-7 have anti-integrase activity with IC50 < 100 micromol L(-1).


Assuntos
Integrase de HIV , Metabolismo , Inibidores de Integrase de HIV , Química , Farmacologia , Concentração Inibidora 50 , Quinolonas , Química , Farmacologia , Relação Estrutura-Atividade
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