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卡罗内酯策略无效:卡罗内酯的合成与生物学评价

The carolactam strategy is ineffective: synthesis and biological evaluation of carolactam.

作者信息

Ammermann Jonas, Schmidt Thomas, Donner Jannik, Reck Michael, Dalton Marly, Stumpp Nico, Stiesch Meike, Wagner-Döbler Irene, Kirschning Andreas

机构信息

Institute of Organic Chemistry and Center of Biomolecular Drug Research (BMWZ), Leibniz Universität Hannover, Schneiderberg 1B, 30167 Hannover, Germany.

出版信息

Org Biomol Chem. 2017 Oct 18;15(40):8553-8558. doi: 10.1039/c7ob02060k.

Abstract

Carolacton, a secondary metabolite isolated from the extracts of Sorangium cellulosum, causes membrane damage and cell death in biofilms of the caries- and endocarditis-associated bacterium Streptococcus mutans and Streptococcus pneumoniae. It is known that macrolactam derivatives can show improved pharmacological properties compared to the corresponding macrolactons (lactam strategy). Therefore, we here report the total synthesis and biological activity of the lactam derivative of carolacton ("carolactam"). Carolactam was inactive against planktonic cultures of S. pneumoniae and caused damage of S. mutans biofilms at high concentrations only (above 10 μM). Preliminary modeling studies indicate substantial conformational differences between carolacton and carolactam.

摘要

从纤维堆囊菌提取物中分离出的次级代谢产物卡罗内酯,可导致与龋齿和心内膜炎相关的变形链球菌和肺炎链球菌生物膜出现膜损伤和细胞死亡。已知与相应的大环内酯(内酰胺策略)相比,大环内酰胺衍生物可表现出更好的药理特性。因此,我们在此报告卡罗内酯的内酰胺衍生物(“卡罗内酰胺”)的全合成及其生物活性。卡罗内酰胺对肺炎链球菌的浮游培养物无活性,仅在高浓度(高于10 μM)时会对变形链球菌生物膜造成损伤。初步的模型研究表明卡罗内酯和卡罗内酰胺之间存在显著的构象差异。

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