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机械化学法合成吡嗪酰胺配位骨架的抗菌活性。

Antimicrobial Activity of Pyrazinamide Coordination Frameworks Synthesized by Mechanochemistry.

机构信息

Centro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal.

Associação do Instituto Superior Técnico para a Investigação e Desenvolvimento (IST-ID), Av. Rovisco Pais, 1049-003 Lisboa, Portugal.

出版信息

Molecules. 2021 Mar 28;26(7):1904. doi: 10.3390/molecules26071904.

Abstract

The urge for the development of a more efficient antibiotic crystalline forms led us to the disclosure of new antibiotic coordination frameworks of pyrazinamide, a well-known drug used for the treatment of tuberculosis, with some of the novel compounds unravelling improved antimycobacterial activity. Mechanochemistry was the preferred synthetic technique to yield novel compounds, allowing the reproduction of a 1D zinc framework, the synthesis of a novel hydrogen bonding manganese framework, and three new compounds with silver. The structural characterization of the novel forms is presented along with stability studies. The increased antimicrobial activity of the new silver-based frameworks against , and is particularly relevant.

摘要

对开发更高效抗生素晶体形式的渴望促使我们发现了新的吡嗪酰胺抗生素配位框架,吡嗪酰胺是一种用于治疗结核病的知名药物,其中一些新型化合物展现出了改善的抗分枝杆菌活性。机械化学是生成新型化合物的首选合成技术,允许复制一维锌框架、合成新型氢键锰框架以及三种新的含银化合物。本文介绍了新型形式的结构特征和稳定性研究。新型银基框架对 、 和 的抗菌活性增强尤其相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab3/8036749/e0ba26749261/molecules-26-01904-g001.jpg

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