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新型 2-氨基噻唑类似物兼具多黏菌素 E 增效剂和抗多重耐药革兰阳性菌的抗菌作用。

Novel 2-aminothiazole analogues both as polymyxin E synergist and antimicrobial agent against multidrug-resistant Gram-positive bacteria.

机构信息

Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, 200237, PR China.

Shanghai JiaoTong University, School of Pharmacy, Shanghai, 200240, PR China.

出版信息

Eur J Med Chem. 2024 Dec 5;279:116879. doi: 10.1016/j.ejmech.2024.116879. Epub 2024 Sep 16.

Abstract

The widespread emergence of antibiotic resistance poses a substantial challenge to global health. While polymyxin E serves as a final option in treatment, its effectiveness is hindered by dose-related toxicity. A crucial strategy for addressing this issue involves incorporating an antibiotic adjuvant to enhance the antibiotic's efficacy and decrease the required dosage. Here, we reported a multifunctional antibacterial compound A33, containing a 2-aminothiazole scaffold. In vitro studies demonstrated that A33 in combination with polymyxin E inhibited the growth of various Gram-negative bacteria, meanwhile with minimum inhibitory concentrations (MICs) of 0.5-4 μg/mL against twenty-three Gram-positive bacteria, including two drug-resistant strains. In vivo studies showed significant efficacy of the combined treatment of A33 and polymyxin E in a mouse infection model. The mice treated with compound A33 (64 mg/kg) and polymyxin E (0.5 mg/kg) in combination had a 100 % survival rate. Mechanistic studies suggested that A33 might exert its synergistic effect by targeting the outer membrane of Gram-negative bacteria. The ADMET data demonstrated that A33 possessed good pharmacokinetic profiles and drug-likeness properties. Overall, the optimized compound A33 assisted polymyxin E in combating various Gram-negative bacteria and exhibited bactericidal effects against drug-resistant Gram-positive bacteria, offering a new potential therapeutic approach for managing mixed bacterial infections.

摘要

抗生素耐药性的广泛出现对全球健康构成了重大挑战。多粘菌素 E 作为治疗的最后选择,但由于剂量相关的毒性而使其效果受到限制。解决这个问题的一个关键策略是加入抗生素佐剂来增强抗生素的疗效并减少所需剂量。在这里,我们报道了一种包含 2-氨基噻唑支架的多功能抗菌化合物 A33。体外研究表明,A33 与多粘菌素 E 联合抑制了各种革兰氏阴性菌的生长,同时对 23 种革兰氏阳性菌(包括两种耐药株)的最小抑菌浓度(MIC)为 0.5-4μg/mL。体内研究表明,A33 和多粘菌素 E 的联合治疗在小鼠感染模型中具有显著疗效。用化合物 A33(64mg/kg)和多粘菌素 E(0.5mg/kg)联合治疗的小鼠的存活率为 100%。机制研究表明,A33 可能通过靶向革兰氏阴性菌的外膜发挥协同作用。ADMET 数据表明,A33 具有良好的药代动力学特性和类药性。总的来说,优化后的化合物 A33 辅助多粘菌素 E 对抗各种革兰氏阴性菌,并对耐药革兰氏阳性菌表现出杀菌作用,为治疗混合细菌感染提供了一种新的潜在治疗方法。

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