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合成含 1,3-二芳基吡唑基部分的新型二氢三嗪衍生物作为潜在的抗菌剂。

Synthesis of novel dihydrotriazine derivatives bearing 1,3-diaryl pyrazole moieties as potential antibacterial agents.

机构信息

Department of Pharmacy, Jilin Medical University, Jilin, Jilin Province 132013, PR China.

Key Laboratory of Natural Resources and Functional Molecules of the Changbai Mountain, Affiliated Ministry of Education, Yanbian University College of Pharmacy, Yanji, Jilin Province 133002, PR China.

出版信息

Bioorg Med Chem Lett. 2019 May 1;29(9):1079-1084. doi: 10.1016/j.bmcl.2019.02.033. Epub 2019 Feb 28.

Abstract

Three novel series of dihydrotriazine derivatives bearing 1,3-diaryl pyrazole moieties were designed, synthesized and evaluated in terms of their antibacterial and antifungal activities. Most of the synthesized compounds showed potent inhibition of several Gram-positive bacterial strains (including multidrug-resistant clinical isolates) and Gram-negative bacterial strains with minimum inhibitory concentration values in the range of 1-64 µg/mL. Compounds 4b and 4c presented the most potent inhibitory activity against Gram-positive bacteria (S. aureus 4220, MRSA 3167, QRSA 3519) and Gram-negative bacteria (E. coli 1924), with minimum inhibitory concentration values of 1 or 2 µg/mL. Compared with previous studies, these compounds exhibited a broad spectrum of inhibitory activity. The cytotoxic activity of the compounds 4a, 4b, 4c and 11n were assessed in L02 cells. In vitro enzyme study implied that compound 4c exerted its antibacterial activity through DHFR inhibition.

摘要

设计、合成并评价了三个新型系列的含 1,3-二芳基吡唑部分的二氢三嗪衍生物,评估其抗菌和抗真菌活性。大多数合成化合物对几种革兰氏阳性菌(包括多药耐药临床分离株)和革兰氏阴性菌具有很强的抑制作用,最小抑菌浓度值在 1-64μg/mL 范围内。化合物 4b 和 4c 对革兰氏阳性菌(金黄色葡萄球菌 4220、MRSA 3167、QRSA 3519)和革兰氏阴性菌(大肠杆菌 1924)表现出最强的抑制活性,最小抑菌浓度值为 1 或 2μg/mL。与以前的研究相比,这些化合物表现出广谱的抑制活性。在 L02 细胞中评估了化合物 4a、4b、4c 和 11n 的细胞毒性。体外酶研究表明,化合物 4c 通过 DHFR 抑制发挥其抗菌活性。

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