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合成 3,5-双(三氟甲基)苯基取代吡唑衍生物作为耐药菌的有效生长抑制剂。

Synthesis of 3,5-Bis(trifluoromethyl)phenyl-Substituted Pyrazole Derivatives as Potent Growth Inhibitors of Drug-Resistant Bacteria.

机构信息

Department of Chemistry and Physics, The College of Sciences and Mathematics, Arkansas State University, Jonesboro, AR 72401, USA.

Department of Biological Sciences, The College of Sciences and Mathematics, Arkansas State University, Jonesboro, AR 72401, USA.

出版信息

Molecules. 2021 Aug 22;26(16):5083. doi: 10.3390/molecules26165083.

Abstract

Enterococci and methicillin-resistant (MRSA) are among the menacing bacterial pathogens. Novel antibiotics are urgently needed to tackle these antibiotic-resistant bacterial infections. This article reports the design, synthesis, and antimicrobial studies of 30 novel pyrazole derivatives. Most of the synthesized compounds are potent growth inhibitors of planktonic Gram-positive bacteria with minimum inhibitory concertation (MIC) values as low as 0.25 µg/mL. Further studies led to the discovery of several lead compounds, which are bactericidal and potent against MRSA persisters. Compounds , , and are potent against biofilms with minimum biofilm eradication concentration (MBEC) values as low as 1 µg/mL.

摘要

肠球菌和耐甲氧西林金黄色葡萄球菌 (MRSA) 是具有威胁性的细菌病原体。急需新型抗生素来应对这些对抗生素具有耐药性的细菌感染。本文报道了 30 种新型吡唑衍生物的设计、合成和抗菌研究。大多数合成的化合物对浮游革兰氏阳性菌具有很强的生长抑制作用,最低抑菌浓度 (MIC) 值低至 0.25 µg/mL。进一步的研究发现了几种具有杀菌作用的先导化合物,对 MRSA 持久菌具有很强的作用。化合物 、 和 对生物膜具有很强的作用,最低生物膜清除浓度 (MBEC) 值低至 1 µg/mL。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/412e/8398255/2e74503a1986/molecules-26-05083-g001.jpg

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