A historical sketch of the discovery and development of HIV-1 integrase inhibitors

被引:106
作者
Savarino, Andrea [1 ]
机构
[1] Ist Super Sanita, Dept Infect Parasit & Immunemediated Dis, I-00161 Rome, Italy
关键词
beta-hydroxyketo group; antiretroviral agent; diketo acid; equisetin; Fusarium; naphtyridine carboxamide; quinolone; strand transfer;
D O I
10.1517/13543784.15.12.1507
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The long process of HIV-1 integrase inhibitor discovery and development can be attributed to both the complexity of HIV-1 integration and poor 'integration' of these researches into mainstream investigations on anti-retroviral therapy in the mid-1990s. Of note, some fungal extracts investigated during this period contain the beta-hydroxyketo group, later recognised to be a key structural requirement for keto-enol acids (also referred to as diketo acids) and other integrase inhibitors. This review reconstructs (in the general context of the history of AIDS research) the principal steps that led to the integrase inhibitors currently in clinical trials, and discusses possible future directions.
引用
收藏
页码:1507 / 1522
页数:16
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