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Design, synthesis and biological evaluation of heteroaryl diketohexenoic and diketobutanoic acids as HIV-1 integrase inhibitors endowed with antiretroviral activity

…, M Artico, R Ragno, G Greco, E Novellino, C Marchand…

文献索引：Di Santo; Costi; Artico; Ragno; Greco; Novellino; Marchand; Pommier Farmaco, 2005 , vol. 60, # 5 p. 409 - 417

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被引用次数: 43

摘要

Highly active anti-retroviral therapy (HAART) using reverse transcriptase (RT) and protease (PR) inhibitors and, more recently, inhibitors of the fusion is currently the best clinical approach in combating acquired immunodeficiency syndrome (AIDS), caused by infection from human immunodeficiency virus type 1 (HIV-1). However, this therapy does not completely eradicate the virus, so that resistant strains easily emerge. The above problem ...