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酰基磺胺:设计新型磺胺类药物类似物的重要基团。

-Acylsulfonamide: a valuable moiety to design new sulfa drug analogues.

作者信息

Amador Romain, Tahrioui Ali, Barreau Magalie, Lesouhaitier Olivier, Smietana Michael, Clavé Guillaume

机构信息

Institut des Biomolécules Max Mousseron, Université de Montpellier, CNRS, ENSCM 1919 route de Mende 34095 Montpellier France

Univ Rouen Normandie, Université Caen Normandie, Normandie Univ, Communication Bactérienne et Stratégies Anti-infectieuses (CBSA) UR 4312 F-76000 Rouen France.

出版信息

RSC Med Chem. 2023 Jul 4;14(8):1567-1571. doi: 10.1039/d3md00229b. eCollection 2023 Aug 16.

Abstract

Sulfonamides are the oldest class of antibiotics, discovered more than 80 years ago. They are still used today despite the appearance of drug resistance phenomena that limit their prescription. Since the discovery and use of the first sulfa drugs, many analogues have been synthesized in order to obtain new active molecules able to circumvent bacterial resistance. Structurally similar to sulfonamide, the -acylsulfonamide group arouses interest in the field of medicinal chemistry due to specific physico-chemical properties. We report here the synthesis and antibacterial/antibiofilm activities of 18 sulfa drug analogues with an -acylsulfonamide moiety. These derivatives were obtained efficiently by sulfo-click reactions between readily available thioacid and sulfonyl azide synthons.

摘要

磺胺类药物是最古老的一类抗生素,于80多年前被发现。尽管出现了限制其处方使用的耐药现象,但它们如今仍在使用。自第一种磺胺药物被发现和使用以来,人们合成了许多类似物,以获得能够规避细菌耐药性的新活性分子。-酰基磺胺基团在结构上与磺胺类药物相似,由于其特定的物理化学性质,在药物化学领域引起了人们的兴趣。我们在此报告了18种具有-酰基磺胺部分的磺胺类药物类似物的合成及其抗菌/抗生物膜活性。这些衍生物是通过容易获得的硫代酸和磺酰叠氮合成子之间的硫醇点击反应高效制备的。

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