Famiglini Valeria, Silvestri Romano
Department of Drug Chemistry and Technologies, Sapienza University of Rome, Laboratory affiliated to Istituto Pasteur Italia - Fondazione Cenci Bolognetti, Roma, Italy.
Antivir Chem Chemother. 2018 Jan-Dec;26:2040206617753443. doi: 10.1177/2040206617753443.
Indolylarylsulfones are a potent class of human immunodeficiency virus type 1 non-nucleoside reverse transcriptase inhibitors. In this review, the structure activity relationship (SAR) studies to improve the profile of sulfone L-737,126 discovered by Merck AG have been analysed with focus on introduction of the 3',5'-dimethyl groups at the 3-phenylsulfonyl moiety, the 2-hydroxyethyl tail at the indole-2-carboxamide nitrogen, coupling of the carboxamide nitrogen with one or two glycinamide and alaninamide units, a fluorine atom at position 4 of the indole ring and correlation between configuration of the asymmetric centre and linker length. IAS derivatives look like promising drug candidates for the treatment of AIDS and related infections in combination with other antiretroviral agents.
吲哚芳基砜是一类有效的1型人类免疫缺陷病毒非核苷逆转录酶抑制剂。在本综述中,已对旨在改善默克公司发现的砜L-737,126特性的构效关系(SAR)研究进行了分析,重点关注在3-苯磺酰基部分引入3',5'-二甲基基团、在吲哚-2-甲酰胺氮上引入2-羟乙基尾、将甲酰胺氮与一个或两个甘氨酰胺和丙氨酰胺单元偶联、在吲哚环4位引入氟原子以及不对称中心构型与连接子长度之间的相关性。吲哚芳基砜衍生物看起来是与其他抗逆转录病毒药物联合用于治疗艾滋病及相关感染的有前景的候选药物。