Synthesis, and docking studies of novel tetrazole-S-alkyl derivatives as antimicrobial agents
作者:Ulviye Acar Çevik、Ismail Celik、Ayşen Işık、Ülküye Dudu Gül、Gizem Bayazıt、Hayrani Eren Bostancı、Yusuf Özkay、Zafer Asım Kaplancıklı
DOI:10.1080/10426507.2022.2117812
日期:2023.2.1
drug, with a MIC value of 7.81 µg/mL. All the derivatives were efficiently synthesized by a two-step process. The structure of the newly synthesized compounds was elucidated by their 1H NMR, 13C NMR, LC-MS/MS, and elemental analysis. In this study, the detailed synthesis, spectroscopic and biological evaluation data are reported. Molecular docking studies of all compounds were performed with the sterol
摘要 合成了一系列新型四唑-S-烷基-哌嗪衍生物,并评估了它们对白色念珠菌(ATCC 24433)、克柔念珠菌(ATCC 6258) 和近光滑念珠菌(ATCC 22019) 的抗真菌活性以及对大肠杆菌的抗菌活性。大肠杆菌(ATCC 25922)、粘质链球菌 ( ATCC 8100)、肺炎克雷伯菌(ATCC 13883)、铜绿假单胞菌(ATCC 27853)、粪肠球菌(ATCC 2942)、枯草杆菌(ATCC)、金黄色葡萄球菌(ATCC ) 29213)、表皮葡萄球菌(ATCC 12228)。在合成的化合物中,1-(4-环己基哌嗪-1-基)-2-((1-甲基-1 H-tetrazol-5-yl)thio)ethan-1-one ( 2b ) (MIC = 7.81 µg/mL) 和 1-(4-(4-chlorobenzyl)piperazin-1-yl)-2-((1-methyl -1 H