Drugs anti-HIV: Past, present and future perspectives.

被引:71
|
作者
de Souza, MVN
de Almeida, MV
机构
[1] Inst Tecnol & Farmacos Far Manguinhos, Fundacao Oswaldo Cruz, BR-21041250 Rio De Janeiro, Brazil
[2] Univ Fed Juiz de Fora, Inst Ciencias Exatas, Dept Quim, BR-36038330 Juiz De Fora, MG, Brazil
来源
QUIMICA NOVA | 2003年 / 26卷 / 03期
关键词
AIDS; new Anti-HIV drugs; replicative cycle;
D O I
10.1590/S0100-40422003000300014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
DRUGS ANTI-HIV: PAST, PRESENT AND FUTURE PERSPECTIVES. Currently available anti-HIV drugs can be classified into three categories: nucleoside analogue reverse transcriptase inhibitors (NRTIs), non-nucleoside reverse transcriptase inhibitors (NNRTIs) and protease inhibitors (PIs). In addition to the reverse transcriptase (RT) and protease reaction, various other events in the HIV replicative cycle can be considered as potential targets for chemotherapeutic intervention: (1) viral adsorption, through binding to the viral envelope glycoprotein gp120; (2) viral entry, through blockage of the viral coreceptors CXCR4 and CCR5; (3) virus-cell fusion, through binding to the viral envelope glycoprotein gp 41; (4) viral assembly and disassembly through NCp7 zinc finger-targeted agents; (5) proviral DNA integration, through integrase inhibitors and (6) viral mRNA transcription, through inhibitors of the transcription (transactivation) process. Also, various new NRTIs, NNRTIs and PIs have been developed, possessing different improved characteristics.
引用
收藏
页码:366 / 372
页数:7
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