Suppr超能文献

具有体内杀菌抗结核活性的含氮氧化物杂环的设计、合成与表征

Design, Synthesis, and Characterization of N-Oxide-Containing Heterocycles with in Vivo Sterilizing Antitubercular Activity.

作者信息

Dos Santos Fernandes Guilherme Felipe, de Souza Paula Carolina, Moreno-Viguri Elsa, Santivañez-Veliz Mery, Paucar Rocio, Pérez-Silanes Silvia, Chegaev Konstantin, Guglielmo Stefano, Lazzarato Loretta, Fruttero Roberta, Man Chin Chung, da Silva Patricia Bento, Chorilli Marlus, Solcia Mariana Cristina, Ribeiro Camila Maríngolo, Silva Caio Sander Paiva, Marino Leonardo Biancolino, Bosquesi Priscila Longhin, Hunt Debbie M, de Carvalho Luiz Pedro S, de Souza Costa Carlos Alberto, Cho Sang Hyun, Wang Yuehong, Franzblau Scott Gary, Pavan Fernando Rogério, Dos Santos Jean Leandro

机构信息

São Paulo State University (UNESP) , Institute of Chemistry, Araraquara 14800060, Brazil.

São Paulo State University (UNESP) , School of Pharmaceutical Sciences, Araraquara 14800903, Brazil.

出版信息

J Med Chem. 2017 Oct 26;60(20):8647-8660. doi: 10.1021/acs.jmedchem.7b01332. Epub 2017 Oct 16.

Abstract

Tuberculosis, caused by Mycobacterium tuberculosis (Mtb), is the infectious disease responsible for the highest number of deaths worldwide. Herein, 22 new N-oxide-containing compounds were synthesized followed by in vitro and in vivo evaluation of their antitubercular potential against Mtb. Compound 8 was found to be the most promising compound, with MIC values of 1.10 and 6.62 μM against active and nonreplicating Mtb, respectively. Additionally, we carried out in vivo experiments to confirm the safety and efficacy of compound 8; the compound was found to be orally bioavailable and highly effective, leading to a reduction of Mtb to undetectable levels in a mouse model of infection. Microarray-based initial studies on the mechanism of action suggest that compound 8 blocks translation. Altogether, these results indicate that benzofuroxan derivative 8 is a promising lead compound for the development of a novel chemical class of antitubercular drugs.

摘要

由结核分枝杆菌(Mtb)引起的结核病是全球致死人数最多的传染病。在此,合成了22种新的含N-氧化物的化合物,并对其抗结核分枝杆菌的潜力进行了体外和体内评估。发现化合物8是最有前景的化合物,对活性和非复制性结核分枝杆菌的MIC值分别为1.10和6.62μM。此外,我们进行了体内实验以确认化合物8的安全性和有效性;该化合物被发现具有口服生物利用度且高效,在感染小鼠模型中可将结核分枝杆菌减少到检测不到的水平。基于微阵列的作用机制初步研究表明化合物8阻断翻译。总之,这些结果表明苯并呋咱衍生物8是开发新型抗结核化学类药物的有前景的先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead3/5677254/57e594a44337/jm-2017-01332v_0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验