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Acta Pharmaceutica Sinica ; (12): 263-267, 2010.
Article in Chinese | WPRIM | ID: wpr-250632

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)
HIV Integrase , Metabolism , HIV Integrase Inhibitors , Chemistry , Pharmacology , Inhibitory Concentration 50 , Quinolones , Chemistry , Pharmacology , Structure-Activity Relationship
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