HIV-1 IN Inhibitors: 2010 Update and Perspectives

被引:80
作者
Marchand, Christophe [1 ]
Maddali, Kasthuraiah [1 ]
Metifiot, Mathieu [1 ]
Pommier, Yves [1 ]
机构
[1] NCI, Mol Pharmacol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
HIV-1; IN; diketo acids; HIV inhibitors; AIDS; IN inhibitors; peptides; oligonucleotides; HUMAN-IMMUNODEFICIENCY-VIRUS; RETROVIRAL DNA-INTEGRATION; CHAIN VARIABLE FRAGMENT; L-CHICORIC ACID; METAL-DEPENDENT INHIBITION; STRAND TRANSFER-REACTION; N-TERMINAL DOMAIN; REVERSE-TRANSCRIPTASE; TYPE-1; INTEGRASE; DUAL INHIBITORS;
D O I
10.2174/156802609789630910
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Integrase (IN) is the newest validated target against AIDS and retroviral infections. The remarkable activity of raltegravir (Isentress (R)) led to its rapid approval by the FDA in 2007 as the first IN inhibitor. Several other IN strand transfer inhibitors (STIs) are in development with the primary goal to overcome resistance due to the rapid occurrence of IN mutations in raltegravir-treated patients. Thus, many scientists and drug companies are actively pursuing clinically useful IN inhibitors. The objective of this review is to provide an update on the IN inhibitors reported in the last two years, including second generation STI, recently developed hydroxylated aromatics, natural products, peptide, antibody and oligonucleotide inhibitors. Additionally, the targeting of IN cofactors such as LEDGF and Vpr will be discussed as novel strategies for the treatment of AIDS.
引用
收藏
页码:1016 / 1037
页数:22
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