Literature DB >> 15193138

Recent advances in the development of next generation non-nucleoside reverse transcriptase inhibitors.

Christine M Tarby1.   

Abstract

Since their discovery, non-nucleoside reverse transcriptase inhibitors (NNRTIs) have become one of the cornerstones of highly active anti-retroviral therapy (HAART). Currently, three NNRTI agents, efavirenz, nevirapine and delavirdine are commercially available. Efavirenz and nevirapine, used in combination with nucleoside reverse transcriptase inhibitors (NRTIs), provide durable regimens with efficacy comparable to protease inhibitor (PI) containing therapies. When virological failure occurs following treatment with an NNRTI, the resistance mutations can confer reduced sensitivity to the entire agent class. Therefore, the strategy for the development of next generation NNRTIs has been to focus on compounds which have improved potencies against the clinically relevant viral mutants. Agents with improved virological profiles and which maintain the ease of administration and favorable safety profiles of the current agents should find use in anti-retroviral naïve patients as well as in components of salvage regimens in the anti-retroviral experienced patient. This review summarizes the recent developments with compounds in clinical trials as of January 2002 as well as to summarize information on new agents appearing in the primary and patent literature between January 2001 and December 2002.

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Year:  2004        PMID: 15193138     DOI: 10.2174/1568026043388295

Source DB:  PubMed          Journal:  Curr Top Med Chem        ISSN: 1568-0266            Impact factor:   3.295


  6 in total

1.  Design, synthesis, and biological evaluation of 1-[(2-benzyloxyl/alkoxyl)methyl]-5-halo-6-aryluracils as potent HIV-1 non-nucleoside reverse transcriptase inhibitors with an improved drug resistance profile.

Authors:  Xiaowei Wang; Jianfang Zhang; Yang Huang; Ruiping Wang; Liang Zhang; Kang Qiao; Li Li; Chang Liu; Yabo Ouyang; Weisi Xu; Zhili Zhang; Liangren Zhang; Yiming Shao; Shibo Jiang; Liying Ma; Junyi Liu
Journal:  J Med Chem       Date:  2012-02-17       Impact factor: 7.446

2.  The HEPT Analogue WPR-6 Is Active against a Broad Spectrum of Nonnucleoside Reverse Transcriptase Drug-Resistant HIV-1 Strains of Different Serotypes.

Authors:  Weisi Xu; Jianxiong Zhao; Jianping Sun; Qianqian Yin; Yan Wang; Yang Jiao; Junyi Liu; Shibo Jiang; Yiming Shao; Xiaowei Wang; Liying Ma
Journal:  Antimicrob Agents Chemother       Date:  2015-06-08       Impact factor: 5.191

3.  Design, synthesis, and anti-HIV-1 activity of 1-substituted 3-(3,5-dimethylbenzyl)triazine derivatives.

Authors:  Norikazu Sakakibara; Gianfranco Balboni; Cenzo Congiu; Valentina Onnis; Yosuke Demizu; Takashi Misawa; Masaaki Kurihara; Yoshihisa Kato; Tokumi Maruyama; Masaaki Toyama; Mika Okamoto; Masanori Baba
Journal:  Antivir Chem Chemother       Date:  2015-10-28

4.  Physicochemical property-driven optimization of diarylaniline compounds as potent HIV-1 non-nucleoside reverse transcriptase inhibitors.

Authors:  Na Liu; Bingjie Qin; Lian-Qi Sun; Fei Yu; Lu Lu; Shibo Jiang; Kuo-Hsiung Lee; Lan Xie
Journal:  Bioorg Med Chem Lett       Date:  2014-07-11       Impact factor: 2.823

5.  The development and validation of an UHPLC-MS/MS method for the rapid quantification of the antiretroviral agent dapivirine in human plasma.

Authors:  Lauren A Seserko; Joshua F Emory; Craig W Hendrix; Mark A Marzinke
Journal:  Bioanalysis       Date:  2013-11       Impact factor: 2.681

6.  Concentrations of dapivirine in the rhesus macaque and rabbit following once daily intravaginal administration of a gel formulation of [14C]dapivirine for 7 days.

Authors:  Jeremy P Nuttall; Daryl C Thake; Mark G Lewis; John W Ferkany; Joseph W Romano; Mark A Mitchnick
Journal:  Antimicrob Agents Chemother       Date:  2007-12-17       Impact factor: 5.191

  6 in total

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