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-甲基硫代缩氨基脲类化合物作为抗菌剂和细菌碳酸酐酶抑制剂的生物研究。

Biological investigation of -methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors.

机构信息

Department of Pharmacy, "G. d'Annunzio" University of Chieti-Pescara, Chieti, Italy.

Department of Pharmacology, Grace College of Pharmacy, Palakkad, India.

出版信息

J Enzyme Inhib Med Chem. 2022 Dec;37(1):986-993. doi: 10.1080/14756366.2022.2055009.

Abstract

The enormous burden of the COVID-19 pandemic in economic and healthcare terms has cast a shadow on the serious threat of antimicrobial resistance, increasing the inappropriate use of antibiotics and shifting the focus of drug discovery programmes from antibacterial and antifungal fields. Thus, there is a pressing need for new antimicrobials involving innovative modes of action (MoAs) to avoid cross-resistance rise. Thiosemicarbazones (TSCs) stand out due to their easy preparation and polypharmacological application, also in infectious diseases. Recently, we reported a small library of TSCs () that emerged for their non-cytotoxic behaviour. Inspired by their multifaceted activity, we investigated the antibacterial, antifungal, and antidermatophytal profiles of derivatives , highlighting a new promising research line. Furthermore, the ability of these compounds to inhibit selected microbial and human carbonic anhydrases (CAs) was assessed, revealing their possible involvement in the MoA and a good selectivity index for some derivatives.

摘要

新型噻唑烷酮类衍生物的抗菌、抗真菌和抗皮肤真菌活性及对人源和微生物碳酸酐酶的抑制作用

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c0/8956313/1e959ccc6a3a/IENZ_A_2055009_UF0001_C.jpg

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