Indolylarylsulfones, a fascinating story of highly potent human immunodeficiency virus type 1 non-nucleoside reverse transcriptase inhibitors.

Q2 Pharmacology, Toxicology and Pharmaceutics Antiviral Chemistry and Chemotherapy Pub Date : 2018-01-01 DOI:10.1177/2040206617753443
Valeria Famiglini, Romano Silvestri
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引用次数: 14

Abstract

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.

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吲哚芳基砜,一个引人入胜的故事,高效的人类免疫缺陷病毒1型非核苷逆转录酶抑制剂。
吲哚芳基砜是一类有效的人类免疫缺陷病毒1型非核苷逆转录酶抑制剂。本文综述了为改善默克公司发现的L-737,126砜的结构活性关系(SAR)研究,重点介绍了在3-苯基磺酰基部分引入3′,5′-二甲基,在吲哚-2-羧基酰胺氮上引入2-羟乙基尾,在羧基酰胺氮上偶联一个或两个甘氨酸酰胺和丙氨酸酰胺单元。吲哚环第4位氟原子及不对称中心构型与连接体长度的关系。IAS衍生物看起来是与其他抗逆转录病毒药物联合治疗艾滋病和相关感染的有希望的候选药物。
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来源期刊
Antiviral Chemistry and Chemotherapy
Antiviral Chemistry and Chemotherapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.20
自引率
0.00%
发文量
5
审稿时长
15 weeks
期刊介绍: Antiviral Chemistry & Chemotherapy publishes the results of original research concerned with the biochemistry, mode of action, chemistry, pharmacology and virology of antiviral compounds. Manuscripts dealing with molecular biology, animal models and vaccines are welcome. The journal also publishes reviews, pointers, short communications and correspondence.
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