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磷化硫属化合物及其由红磷与功能化吡啶、咪唑、吡唑生成的衍生物及其抗菌和细胞抑制活性。

Phosphine chalcogenides and their derivatives from red phosphorus and functionalized pyridines, imidazoles, pyrazoles and their antimicrobial and cytostatic activity.

作者信息

Malysheva Svetlana, Kuimov Vladimir, Belovezhets Lyudmila, Belogorlova Natalia, Borovskaya Marina, Borovskii Gennadii

机构信息

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St., 664033 Irkutsk, Russia.

Siberian Institute of Plant Physiology and Biochemistry, Siberian Brunch of the Russian Academy of Sciences, Lermontova st., 132, Irkutsk, 664033, Russia.

出版信息

Bioorg Chem. 2023 Mar;132:106363. doi: 10.1016/j.bioorg.2023.106363. Epub 2023 Jan 18.

Abstract

Tertiary phosphine oxides, phosphine sulfides, and phosphine selenides containing pyridine, imidazole, and pyrazole groups have been synthesized via the reaction of elemental phosphorus or secondary phosphine oxides with functional pyridines, imidazoles, and pyrazoles. Alkyl tris(2-pyridylethyl)phosphonium iodide and bromide are also obtained by quaternization of the corresponding phosphine. Antimicrobial activity of the synthesized compounds, including nitrogen-containing heterocycles, phosphorus, selenium, and sulfur, with respect to Enterococcus durans, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa microorganisms is evaluated. It is found that phosphine chalcogenides bearing imidazole (14, 19), pyrazole (13), and pyridine fragments (5, 9) and phosphonium salts (11, 12) can be considered as new promising antibacterial agents. For some synthesized compounds, LC is determined. Phosphine oxide with methylpyrazole fragments (13) and phosphonium salts (11, 12) show strong profile of antimicrobial activity, and cytotoxic effect of phosphonium bromide having a long chain radical (12) is by order of magnitude higher than that of cisplatin. We believe that the results obtained may contribute to the development of highly effective agents for the treatment and prevention of bacterial infections and cancers.

摘要

通过元素磷或仲膦氧化物与功能性吡啶、咪唑和吡唑的反应,合成了含有吡啶、咪唑和吡唑基团的叔膦氧化物、膦硫化物和膦硒化物。相应的膦经季铵化反应还可得到烷基三(2 - 吡啶基乙基)碘化膦和溴化膦。评估了所合成的含氮杂环、磷、硒和硫的化合物对耐久肠球菌、枯草芽孢杆菌、大肠杆菌、铜绿假单胞菌等微生物的抗菌活性。发现带有咪唑(14, 19)、吡唑(13)和吡啶片段(5, 9)的膦硫属化物以及鏻盐(11, 12)可被视为有前景的新型抗菌剂。对一些合成化合物测定了最低抑菌浓度(LC)。带有甲基吡唑片段的膦氧化物(13)和鏻盐(11, 12)表现出很强的抗菌活性,具有长链基团的溴化鏻(12)的细胞毒性作用比顺铂高一个数量级。我们认为所获得的结果可能有助于开发用于治疗和预防细菌感染及癌症的高效药物。

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