Selected article for: "drug resistant virus and wild type"

Author: Novikov, Mikhail S.; Ivanova, Olga N.; Ivanov, Alexander V.; Ozerov, Alexander A.; Valuev-Elliston, Vladimir T.; Temburnikar, Kartik; Gurskaya, Galina V.; Kochetkov, Sergey N.; Pannecouque, Christophe; Balzarini, Jan; Seley-Radtke, Katherine L.
Title: 1-[2-(2-Benzoyl- and 2-benzylphenoxy)ethyl]uracils as potent anti-HIV-1 agents
  • Cord-id: 1nk1trsa
  • Document date: 2011_10_1
  • ID: 1nk1trsa
    Snippet: Non-nucleoside reverse transcriptase inhibitors (NNRTI) are key components in highly active antiretroviral therapy for treating HIV-1. Herein we present the synthesis for a series of N1-alkylated uracil derivatives bearing ω-(2-benzyl- and 2-benzoylphenoxy)alkyl substituents as novel NNRTIs. These compounds displayed anti-HIV activity similar to that of nevirapine and several of them exhibited activity against the K103N/Y181C RT mutant HIV-1 strain. Further evaluation revealed that the inhibito
    Document: Non-nucleoside reverse transcriptase inhibitors (NNRTI) are key components in highly active antiretroviral therapy for treating HIV-1. Herein we present the synthesis for a series of N1-alkylated uracil derivatives bearing ω-(2-benzyl- and 2-benzoylphenoxy)alkyl substituents as novel NNRTIs. These compounds displayed anti-HIV activity similar to that of nevirapine and several of them exhibited activity against the K103N/Y181C RT mutant HIV-1 strain. Further evaluation revealed that the inhibitors were active against most nevirapine-resistant mono- and di-substituted RTs with the exception of the V106A RT. Thus, the candidate compounds can be regarded as potential lead compounds against the wild-type virus and drug-resistant forms.

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