One-pot synthesis and antiproliferative activity of novel double-modified derivatives of the polyether ionophore monensin A

被引:6
|
作者
Klejborowska, Greta [1 ]
Maj, Ewa [2 ]
Wietrzyk, Joanna [2 ]
Stefanska, Joanna [3 ]
Huczynski, Adam [1 ]
机构
[1] Adam Mickiewicz Univ, Fac Chem, Umultowska 89b, PL-61614 Poznan, Poland
[2] Polish Acad Sci, Hirszfeld Inst Immunol & Expt Therapy, Wroclaw, Poland
[3] Med Univ Warsaw, Dept Pharmaceut Microbiol, Warsaw, Poland
关键词
antimicrobial activity; antiproliferative activity; drug design; natural compounds; polyether ionophores; MEDIATED GROWTH-INHIBITION; CELL-CYCLE ARREST; BIOLOGICAL EVALUATION; MOLECULAR-STRUCTURE; CANCER CELLS; APOPTOSIS; RESISTANT; COMPLEX; SALINOMYCIN;
D O I
10.1111/cbdd.13320
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Monensin A (MON) is a polyether ionophore antibiotic, which shows a wide spectrum of biological activity. New MON derivatives such as double-modified ester-carbonates and double-modified amide-carbonates were obtained by a new and efficient one-pot synthesis with triphosgene as the activating reagent and the respective alcohol or amine. All new derivatives were tested for their antiproliferative activity against two drug-sensitive (MES-SA, LoVo) and two drug-resistant (MES-SA/DX5, LoVo/DX) cancer cell lines, and were also studied for their antimicrobial activity against different Staphylococcus aureus and Staphylococcus epidermidis bacterial strains. For the first time, the activity of MON and its derivatives against MES-SA and MES-SA/DX5 were evaluated.
引用
收藏
页码:1537 / 1546
页数:10
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