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Chem Pharm Bull (Tokyo) ; 58(7): 976-9, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20606350

ABSTRACT

To search for compounds with superior anti-human immunodeficiency virus type 1 (HIV-1) activity, ten 5,5'-(p-phenylenebisazo)-8-hydroxyquinoline sulfonates (4a-j) were synthesized and preliminarily evaluated as HIV-1 inhibitors in vitro for the first time. Some compounds demonstrated anti-HIV-1 activity, especially 5,5'-(p-phenylenebisazo)-8-hydroxyquinoline p-ethylbenzenesulfonate (4g) and 5,5'-(p-phenylenebisazo)-8-hydroxyquinoline p-chlorobenzenesulfonate (4i) showed the more potent anti-HIV-1 activity with 50% effective concentration (EC(50)) values of 2.59 and 4.01 microg/ml, and therapeutic index (TI) values of 31.77 and 24.51, respectively.


Subject(s)
Anti-HIV Agents/chemical synthesis , HIV-1/drug effects , Hydroxyquinolines/chemistry , Anti-HIV Agents/chemistry , Anti-HIV Agents/toxicity , Cell Line, Tumor , Drug Discovery , Humans , Hydroxyquinolines/chemical synthesis , Hydroxyquinolines/toxicity , Structure-Activity Relationship
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