Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.
Mikrobielle Genetik, Interfakultäres Institut für Mikrobiologie und Infektionsmedizin Tübingen (IMIT), Universität Tübingen, Auf der Morgenstelle 28, 72076, Tübingen, Germany.
Angew Chem Int Ed Engl. 2017 Dec 11;56(50):15852-15856. doi: 10.1002/anie.201707069. Epub 2017 Nov 17.
In the past 20 years, peptide-based antibiotics, such as vancomycin, teicoplanin, and daptomycin, have often been considered as second-line antibiotics. However, in recent years, an increasing number of reports on vancomycin resistance in pathogens appeared, which forces researchers to find novel lead structures for potent new antibiotics. Herein, we report the total synthesis of a defined endo-type B PPAP library and their antibiotic activity against multiresistant S. aureus and various vancomycin-resistant Enterococci. Four new compounds that combine high activities and low cytotoxicity were identified, indicating that the PPAP core might become a new non-peptide-based lead structure in antibiotic research.
在过去的 20 年中,基于肽的抗生素,如万古霉素、替考拉宁和达托霉素,通常被认为是二线抗生素。然而,近年来,越来越多的关于病原体万古霉素耐药性的报道出现,这迫使研究人员寻找新型有效抗生素的先导结构。在此,我们报告了内型 B PPAP 文库的全合成及其对多药耐药性金黄色葡萄球菌和各种万古霉素耐药性肠球菌的抗菌活性。鉴定出了四种兼具高活性和低细胞毒性的新型化合物,这表明 PPAP 核心可能成为抗生素研究中的一种新型非肽类先导结构。