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在52种天然和合成化合物中寻找抗菌活性,鉴定出了具有抑制作用的蒽醌类和聚乙炔类化合物。

Search for Antimicrobial Activity Among Fifty-Two Natural and Synthetic Compounds Identifies Anthraquinone and Polyacetylene Classes That Inhibit .

作者信息

Pollo Luiz A E, Martin Erlon F, Machado Vanessa R, Cantillon Daire, Wildner Leticia Muraro, Bazzo Maria Luiza, Waddell Simon J, Biavatti Maique W, Sandjo Louis P

机构信息

Programa de Pós-Graduação em Farmácia, CCS, Universidade Federal de Santa Catarina, Florianópolis, Brazil.

Department of Global Health and Infection, Brighton and Sussex Medical School, University of Sussex, Brighton, United Kingdom.

出版信息

Front Microbiol. 2021 Jan 18;11:622629. doi: 10.3389/fmicb.2020.622629. eCollection 2020.

Abstract

Drug-resistant tuberculosis threatens to undermine global control programs by limiting treatment options. New antimicrobial drugs are required, derived from new chemical classes. Natural products offer extensive chemical diversity and inspiration for synthetic chemistry. Here, we isolate, synthesize and test a library of 52 natural and synthetic compounds for activity against . We identify seven compounds as antimycobacterial, including the natural products isobavachalcone and isoneorautenol, and a synthetic chromene. The plant-derived secondary metabolite damnacanthal was the most active compound with the lowest minimum inhibitory concentration of 13.07 μg/mL and a favorable selectivity index value. Three synthetic polyacetylene compounds demonstrated antimycobacterial activity, with the lowest MIC of 17.88 μg/mL. These results suggest new avenues for drug discovery, expanding antimicrobial compound chemistries to novel anthraquinone and polyacetylene scaffolds in the search for new drugs to treat drug-resistant bacterial diseases.

摘要

耐多药结核病有可能通过限制治疗选择来破坏全球控制计划。需要从新的化学类别中衍生出新型抗菌药物。天然产物为合成化学提供了广泛的化学多样性和灵感。在此,我们分离、合成并测试了一个包含52种天然和合成化合物的文库,以检测其对……的活性。我们鉴定出七种化合物具有抗分枝杆菌活性,包括天然产物异补骨脂查耳酮和异新奥勒冈醇,以及一种合成色烯。植物衍生的次生代谢产物金丝桃素是活性最强的化合物,最低抑菌浓度为13.07μg/mL,且具有良好的选择性指数值。三种合成聚乙炔化合物表现出抗分枝杆菌活性,最低MIC为17.88μg/mL。这些结果为药物发现开辟了新途径,在寻找治疗耐药细菌性疾病的新药过程中,将抗菌化合物化学扩展到新型蒽醌和聚乙炔支架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aef/7847937/a041686fa809/fmicb-11-622629-g001.jpg

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