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C-2 衍生化 8-磺胺基喹啉类化合物作为抗菌化合物。

C-2 derivatized 8-sulfonamidoquinolines as antibacterial compounds.

机构信息

School of Chemical Sciences, University of Auckland, 23 Symonds Street, Auckland, New Zealand; Maurice Wilkins Centre for Molecular Biodiscovery, University of Auckland, Auckland 1042, New Zealand.

School of Chemical Sciences, University of Auckland, 23 Symonds Street, Auckland, New Zealand.

出版信息

Bioorg Med Chem. 2021 Jan 1;29:115837. doi: 10.1016/j.bmc.2020.115837. Epub 2020 Nov 6.

Abstract

A series of C-2 derivatized 8-sulfonamidoquinolines were evaluated for their antibacterial activity against the common mastitis causative pathogens Streptococcus uberis, Staphylococcus aureus and Escherichia coli, both in the presence and absence of supplementary zinc (50 µM ZnSO). The vast majority of compounds tested were demonstrated to be significantly more active against S. uberis when in the presence of supplementary zinc (MICs as low as 0.125 µg/mL were observed in the presence of 50 µM ZnSO). Compounds 5, 34-36, 39, 58, 79, 82, 94 and 95 were shown to display the greatest antibacterial activity against S. aureus (MIC ≤ 8 µg/mL; both in the presence and absence of supplementary zinc), while compounds 56, 58 and 66 were demonstrated to also exhibit activity against E. coli (MIC ≤ 16 µg/mL; under all conditions). Compounds 56, 58 and 66 were subsequently confirmed to be bactericidal against all three mastitis pathogens studied, with MBCs (≥3log CFU/mL reduction) of ≤ 32 µg/mL (in both the presence and absence of 50 µM ZnSO). To validate the sanitizing activity of compounds 56, 58 and 66, a quantitative suspension disinfection (sanitizer) test was performed. Sanitizing activity (>5log CFU/mL reduction in 5 min) was observed against both S. uberis and E. coli at compound concentrations as low as 1 mg/mL (compounds 56, 58 and 66), and against S. aureus at 1 mg/mL (compound 58); thereby validating the potential of compounds 56, 58 and 66 to function as topical sanitizers designed explicitly for use in non-human applications.

摘要

一系列 C-2 衍生的 8-磺酰胺基喹啉类化合物被评估了其对常见乳腺炎病原体无乳链球菌、金黄色葡萄球菌和大肠杆菌的抗菌活性,同时评估了有无补充锌(50 μM ZnSO)的情况。绝大多数测试化合物在有补充锌的情况下对无乳链球菌的活性显著增强(在 50 μM ZnSO 的存在下,观察到低至 0.125 μg/mL 的 MIC)。化合物 5、34-36、39、58、79、82、94 和 95 对金黄色葡萄球菌显示出最大的抗菌活性(MIC≤8μg/mL;无论有无补充锌),而化合物 56、58 和 66 被证明对大肠杆菌也有活性(MIC≤16μg/mL;在所有条件下)。化合物 56、58 和 66 随后被证实对研究的所有三种乳腺炎病原体均具有杀菌作用,MBC(减少≥3log CFU/mL)≤32μg/mL(在有和没有 50 μM ZnSO 的情况下)。为了验证化合物 56、58 和 66 的消毒活性,进行了定量悬浮消毒(消毒剂)测试。在 1mg/mL(化合物 56、58 和 66)的低浓度下,对无乳链球菌和大肠杆菌均观察到消毒活性(在 5 分钟内减少≥5log CFU/mL),而在 1mg/mL(化合物 58)时对金黄色葡萄球菌也观察到消毒活性;从而验证了化合物 56、58 和 66 具有作为专门用于非人类应用的局部消毒剂的潜力。

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