In vitro screening of 2-(1H-imidazol-1-yl)-1-phenylethanol derivatives as antiprotozoal agents and docking studies on Trypanosoma cruzi CYP51

被引:19
|
作者
De Vita, Daniela [1 ]
Moraca, Francesca [3 ]
Zamperini, Claudio [3 ]
Pandolfi, Fabiana
Di Santo, Roberto [2 ]
Matheeussen, An [4 ]
Maes, Louis [4 ]
Tortorella, Silvano [1 ]
Scipione, Luigi [1 ]
机构
[1] Univ Roma La Sapienza, Dept Chim & Tecnol Farmaco, Piazzale Aldo Moro 5, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, Dept Chim & Tecnol Farmaco, Fdn Cenci Bolognetti, Ist Pasteur, Piazzale Aldo Moro 5, I-00185 Rome, Italy
[3] Univ Siena, Dept Biotecnol Chim & Farm, Via A Moro 2, I-53100 Siena, Italy
[4] Univ Antwerp, Fac Pharmaceut Biomed & Vet Sci, LMPH, B-2610 Antwerp, Belgium
关键词
Trypanosoma cruzi; Azoles; CYP51; CHAGAS-DISEASE; INHIBITORS; DISCOVERY; SERIES;
D O I
10.1016/j.ejmech.2016.02.028
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Sterol 14 alpha-demethylase (CYP51) is a key enzyme involved in the survival and virulence of many parasite protozoa, such as Trypanosoma and Leishmania species, thus representing a valuable drug target for the treatment of Kinetoplastid diseases. A set of azole-based compounds selected from an in-house compound library was in vitro screened against different human protozoan parasites. Several compounds showed selective activity against Trypanosoma cruzi, with compound 7 being the most active (IC50 = 40 nM). Given the structural similarity between the compounds here reported and known CYP51 inhibitors, a molecular docking study was performed to assess their binding with protozoal target and to rationalize the biological activity data. (C) 2016 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:28 / 33
页数:6
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