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Chem Biol Drug Des ; 85(6): 722-8, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25328020

ABSTRACT

A novel series of 1-(thiophen-2-yl)-9H-pyrido [3,4-b]indole derivatives were synthesized using DL-tryptophan as starting material. All the compounds were characterized by spectral analysis such as (1) H NMR, Mass, IR, elemental analysis and evaluated for inhibitory potency against HIV-1 replication. Among the reported analogues, compound 7g exhibited significant anti-HIV activity with EC(50) 0.53 µm and selectivity index 483; compounds 7e, 7i, and 7o displayed moderate activity with EC(50) 3.8, 3.8, and 2.8 µm and selectivity index >105, >105, and 3.85, respectively. Interestingly, compound 7g inhibited p24 antigen expression in acute HIV-1(IIIB) infected cell line C8166 with EC50 1.1 µm. In this study, we also reported the Lipinski rule of 5 parameters, predicted toxicity profile, drug-likeness, and drug score of the synthesized analogues.


Subject(s)
Anti-HIV Agents/chemistry , Anti-HIV Agents/pharmacology , Drug Design , HIV-1/drug effects , Indoles/chemistry , Indoles/pharmacology , Anti-HIV Agents/chemical synthesis , Cell Line , HIV Infections/drug therapy , HIV Infections/virology , HIV-1/physiology , Humans , Indoles/chemical synthesis , Structure-Activity Relationship , Thiophenes/chemical synthesis , Thiophenes/chemistry , Thiophenes/pharmacology , Virus Replication/drug effects
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