Liu Kai, Xia Jing, Li Yun, Li Bing-Bing, Wang Meng-Qian, Zhou Qian, Ma Meng-Lin, He Qiu-Rong, Yang Wei-Qing, Liu Dong-Fang, Wang Zhou-Yu, Yang Ling-Ling, Zhang Yuan-Yuan
School of Science, Xihua University, Chengdu 610039, China.
West China Fourth Hospital, Sichuan University, Chengdu 610041, China.
J Med Chem. 2024 Dec 12;67(23):21030-21048. doi: 10.1021/acs.jmedchem.4c01678. Epub 2024 Nov 27.
Treating methicillin-resistant (MRSA) infection remains one of the most difficult challenges in clinical practice, primarily due to the resistance of MRSA to multiple antibiotics. Therefore, there is an urgent need to develop novel antibiotics with high efficacy and low cross-resistance rates. In this study, a series of novel pleuromutilin derivatives with coumarin structures were synthesized and subsequently assessed for their biological activities. Most of these derivatives showed potent antimicrobial activity against drug-resistant Gram-positive bacterial strains. Compound displayed particularly rapid bactericidal effects, slow resistance development, and low cytotoxicity. Moreover, it decreased bacterial loads in the lung, liver, kidney, spleen, and heart and exhibited better antibacterial efficacy (ED = 11.16 mg/kg) than tiamulin (ED = 28.93 mg/kg) in a mouse model of systemic MRSA infection. Both in vitro and in vivo analyses suggest that compound is a promising agent for the treatment of MRSA infections.
治疗耐甲氧西林金黄色葡萄球菌(MRSA)感染仍然是临床实践中最困难的挑战之一,主要是因为MRSA对多种抗生素具有耐药性。因此,迫切需要开发具有高疗效和低交叉耐药率的新型抗生素。在本研究中,合成了一系列具有香豆素结构的新型截短侧耳素衍生物,并随后评估了它们的生物活性。这些衍生物中的大多数对耐药革兰氏阳性细菌菌株显示出强大的抗菌活性。化合物表现出特别快速的杀菌作用、缓慢的耐药性发展和低细胞毒性。此外,在全身性MRSA感染的小鼠模型中,它降低了肺、肝、肾、脾和心脏中的细菌载量,并且比替米考星(ED = 28.93 mg/kg)表现出更好的抗菌疗效(ED = 11.16 mg/kg)。体外和体内分析均表明,化合物是治疗MRSA感染的有前景的药物。