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硒代亚碲锌(PhSeZnCl)在合成具有抗菌活性的甾体β-羟基-苯硒醚中的应用。

PhSeZnCl in the Synthesis of Steroidal β-Hydroxy-Phenylselenides Having Antibacterial Activity.

机构信息

Institute of Chemistry, University of Białystok, ul. Ciołkowskiego 1K, 15-245 Białystok, Poland.

Department of Microbiological and Nanobiomedical Engineering, Medical University of Białystok, ul. Mickiewicza 2C, 15-222 Bialystok, Poland.

出版信息

Int J Mol Sci. 2019 Apr 29;20(9):2121. doi: 10.3390/ijms20092121.

Abstract

We report here the reaction of in situ prepared PhSeZnCl with steroid derivatives having an epoxide as an electrophilic functionalization. The corresponding ring-opening reaction resulted to be regio- and stereoselective affording to novel phenylselenium-substituted steroids. Assessment of their antibacterial properties against multidrug-resistant bacteria, such as Xen 5 strain, indicates an interesting bactericidal activity and their ability to prevent bacterial biofilm formation.

摘要

我们在这里报告了原位制备的 PhSeZnCl 与具有环氧化物作为亲电官能团的甾体衍生物的反应。相应的开环反应具有区域和立体选择性,得到了新型的苯硒取代甾体。评估它们对多药耐药菌(如 Xen 5 株)的抗菌性能表明,它们具有有趣的杀菌活性和防止细菌生物膜形成的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9d4/6539910/7c51c9f6ecfa/ijms-20-02121-g001.jpg

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