Design and synthesis of amphiphilic 2-hydroxybenzylphosphonium salts with antimicrobial and antitumor dual action

被引:21
|
作者
Terekhova, Natalia, V [1 ]
Tatarinov, Dmitry A. [1 ]
Shaihutdinova, Zukhra M. [2 ]
Pashirova, Tatiana N. [1 ]
Lyubina, Anna P. [1 ]
Voloshina, Alexandra D. [1 ]
Sapunova, Anastasiia S. [1 ]
Zakharova, Lucia Ya [1 ]
Mironov, Vladimir F. [1 ]
机构
[1] RAS, Arbuzov Inst Organ & Phys Chem, FRC Kazan Sci Ctr, Arbuzov Str 8, Kazan 420088, Russia
[2] Kazan Fed Univ, Kremlevskaya Str 18, Kazan 420008, Russia
关键词
Phosphonium salts; Grignard reagents; Antimicrobial activity; Cytotoxicity; Phosphine oxides; Cyclization; Critical micelle concentration; Cytofluorimetry; CATIONIC SURFACTANTS; GEMINI SURFACTANTS; DERIVATIVES; AGGREGATION; BEHAVIOR; OXIDES;
D O I
10.1016/j.bmcl.2020.127234
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Here we report the synthesis and biological evaluation of a series of new 2-hydroxybenzylphosphonium salts (QPS) with antimicrobial and antitumor dual action. The most active compounds exhibit antimicrobial activity at a micromolar level against Gram-positive bacteria Sa (ATCC 209p and clinical isolates), Bc (1-2 mu M) and fungi Tm and Ca, and induced no notable hemolysis at MIC. The change in nature of substituents of the same length led to a drastic change of biological activity. Self-assembly behavior of the octadecyl and oleyl derivatives was studied. QPS demonstrated self-assembly within the micromolar range with the formation of nanosized aggregates capable of the solubilizing hydrophobic probe. The synthesized phosphonium salts were tested for cytotoxicity. The most potent salt was active against on M - Hela cell line with IC50 on the level of doxorubicin and good selectivity. According to the cytofluorimetry analysis, the salts induced mitochondria-dependent apoptosis.
引用
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页数:7
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