Institut des Biomolécules Max Mousseron, Univ Montpellier, CNRS, ENSCM, Montpellier, France.
Dipartimento di Biotecnologie Mediche, Università di Siena, I-53100 Siena, Italy.
Bioorg Med Chem. 2022 Oct 15;72:116964. doi: 10.1016/j.bmc.2022.116964. Epub 2022 Aug 11.
Metallo-β-lactamases (MBLs) represent an increasingly serious threat to public health because of their increased prevalence worldwide in relevant opportunistic Gram-negative pathogens. MBLs efficiently inactivate widely used and most valuable β-lactam antibiotics, such as oxyiminocephalosporins (ceftriaxone, ceftazidime) and the last-resort carbapenems. To date, no MBL inhibitor has been approved for therapeutic applications. We are developing inhibitors characterized by a 1,2,4-triazole-3-thione scaffold as an original zinc ligand and few promising series were already reported. Here, we present the synthesis and evaluation of a new series of compounds characterized by the presence of an arylalkyl substituent at position 4 of the triazole ring. The alkyl link was mainly an ethylene, but a few compounds without alkyl or with an alkyl group of various lengths up to a butyl chain were also synthesized. Some compounds in both sub-series were micromolar to submicromolar inhibitors of tested VIM-type MBLs. A few of them were broad-spectrum inhibitors, as they showed significant inhibitory activity on NDM-1 and, to a lesser extent, IMP-1. Among these, several inhibitors were able to significantly reduce the meropenem MIC on VIM-1- and VIM-4- producing clinical isolates by up to 16-fold. In addition, ACE inhibition was absent or moderate and one promising compound did not show toxicity toward HeLa cells at concentrations up to 250 μM. This series represents a promising basis for further exploration. Finally, molecular modelling of representative compounds in complex with VIM-2 was performed to study their binding mode.
金属β-内酰胺酶(MBLs)在全球范围内在相关机会性革兰氏阴性病原体中的流行率增加,对公共健康构成了日益严重的威胁。MBLs 有效地使广泛使用和最有价值的β-内酰胺抗生素失活,例如氧肟头孢菌素(头孢曲松、头孢他啶)和最后手段碳青霉烯类。迄今为止,尚无 MBL 抑制剂获准用于治疗应用。我们正在开发以 1,2,4-三唑-3-硫酮骨架为特征的抑制剂,作为原始锌配体,已经报道了几个有前途的系列。在这里,我们提出了一系列新化合物的合成和评价,这些化合物的特征是三唑环的 4 位具有芳烷基取代基。烷基连接主要是乙烯,但也合成了一些没有烷基或具有各种长度烷基链(最长可达丁基链)的化合物。两个亚系列中的一些化合物对测试的 VIM 型 MBLs 具有微摩尔至亚微摩尔的抑制作用。其中一些是广谱抑制剂,因为它们对 NDM-1 表现出显著的抑制活性,并且在较小程度上对 IMP-1 表现出抑制活性。在这些抑制剂中,有几种抑制剂能够使产 VIM-1 和 VIM-4 的临床分离株的美罗培南 MIC 降低多达 16 倍。此外,ACE 抑制作用缺失或适中,一种有前途的化合物在高达 250 μM 的浓度下对 HeLa 细胞没有毒性。该系列为进一步探索提供了有希望的基础。最后,对与 VIM-2 形成复合物的代表性化合物进行了分子建模,以研究它们的结合模式。