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Design, synthesis of quinolinone acid-containing compounds with anti-HIV integrase activity / 药学学报
Acta Pharmaceutica Sinica ; (12): 263-267, 2010.
Article in Zh | WPRIM | ID: wpr-250632
Responsible library: WPRO
ABSTRACT
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).
Subject(s)
Full text: 1 Index: WPRIM Main subject: Pharmacology / Structure-Activity Relationship / Chemistry / Quinolones / HIV Integrase Inhibitors / HIV Integrase / Inhibitory Concentration 50 / Metabolism Language: Zh Journal: Acta Pharmaceutica Sinica Year: 2010 Type: Article
Full text: 1 Index: WPRIM Main subject: Pharmacology / Structure-Activity Relationship / Chemistry / Quinolones / HIV Integrase Inhibitors / HIV Integrase / Inhibitory Concentration 50 / Metabolism Language: Zh Journal: Acta Pharmaceutica Sinica Year: 2010 Type: Article