Institute of Organic Chemistry and Macromolecular Chemistry, Faculty of Mathematics and Natural Sciences, Heinrich Heine University Düsseldorf, Universitätsstrasse 1, D-40225 Düsseldorf, Germany.
Institute of Pharmaceutical Biology and Biotechnology, Faculty of Mathematics and Natural Sciences, Heinrich Heine University Düsseldorf, Universitätsstrasse 1, D-40225 Düsseldorf, Germany.
Molecules. 2024 May 3;29(9):2126. doi: 10.3390/molecules29092126.
In this study, a library of 3,7-di(hetero)aryl-substituted 10-(3-trimethylammoniumpropyl)10-phenothiazine salts is prepared. These title compounds and their precursors are reversible redox systems with tunable potentials. The Hammett correlation gives a very good correlation of the first oxidation potentials with σ parameters. Furthermore, the title compounds and their precursors are blue to green-blue emissive. Screening of the salts reveals for some derivatives a distinct inhibition of several pathogenic bacterial strains (, , , , and ) in the lower micromolar range.
在这项研究中,制备了 3,7-二(杂)芳基取代的 10-(三甲基铵丙基)10-吩噻嗪盐的库。这些标题化合物及其前体是具有可调电位的可逆氧化还原体系。Hammett 相关给出了与 σ 参数非常好的第一氧化电位的相关性。此外,标题化合物及其前体具有蓝色至蓝绿色发光性。盐的筛选表明,一些衍生物在较低的微摩尔范围内明显抑制了几种致病菌(,,,,和)。