新型香豆素胸膜残素衍生物作为抗mrsa药物的发现

IF 6.8 1区 医学 Q1 CHEMISTRY, MEDICINAL
Kai Liu, Jing Xia, Yun Li, Bing-Bing Li, Meng-Qian Wang, Qian Zhou, Meng-Lin Ma, Qiu-Rong He, Wei-Qing Yang*, Dong-Fang Liu, Zhou-Yu Wang, Ling-Ling Yang* and Yuan-Yuan Zhang*, 
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引用次数: 0

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)感染的治疗仍然是临床实践中最困难的挑战之一,主要是由于MRSA对多种抗生素的耐药性。因此,迫切需要开发高效、低交叉耐药率的新型抗生素。本研究合成了一系列具有香豆素结构的新型胸膜残素衍生物,并对其生物活性进行了评价。大多数这些衍生物对耐药革兰氏阳性菌株显示出有效的抗菌活性。化合物14b的杀菌效果特别快,耐药发展缓慢,细胞毒性低。此外,在小鼠全身MRSA感染模型中,它能降低肺、肝、肾、脾和心脏的细菌负荷,并表现出更好的抗菌效果(ED50 = 11.16 mg/kg),优于替亚穆林(ED50 = 28.93 mg/kg)。体外和体内分析表明,化合物14b是一种治疗MRSA感染的有希望的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Discovery of Novel Coumarin Pleuromutilin Derivatives as Potent Anti-MRSA Agents

Discovery of Novel Coumarin Pleuromutilin Derivatives as Potent Anti-MRSA Agents

Treating methicillin-resistant Staphylococcus aureus (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 14b 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 (ED50 = 11.16 mg/kg) than tiamulin (ED50 = 28.93 mg/kg) in a mouse model of systemic MRSA infection. Both in vitro and in vivo analyses suggest that compound 14b is a promising agent for the treatment of MRSA infections.

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来源期刊
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry 医学-医药化学
CiteScore
4.00
自引率
11.00%
发文量
804
审稿时长
1.9 months
期刊介绍: The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents. The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.
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