Synthesis and in vitro urease inhibitory activity of N,N′-disubstituted thioureas

被引:102
|
作者
Khan, Khalid Mohammed [1 ]
Naz, Farzana [1 ]
Taha, Muhammad [2 ,4 ]
Khan, Ajmal [1 ]
Perveen, Shahnaz [3 ]
Choudhary, M. I. [1 ]
Voelter, Wolfgang [5 ]
机构
[1] Univ Karachi, HEJ Res Inst Chem, Int Ctr Chem & Biol Sci, Karachi 75270, Pakistan
[2] Univ Teknol MARA UiTM, Atta ur Rahman Inst Nat Prod Discovery, Bandar Puncak Alam 42300, Selangor, Malaysia
[3] PCSIR Labs Complex, Karachi 75280, Pakistan
[4] Fac Appl Sci UiTM, Shah Alam 40450, Selangor, Malaysia
[5] Univ Tubingen, Interfak Inst Biochem, D-72076 Tubingen, Germany
关键词
Thiourea derivatives; Synthesis; In vitro urease inhibition activity; Kinetic study; SCHIFF-BASES; ANTIMICROBIAL ACTIVITY; BIOLOGICAL EVALUATION; HELICOBACTER-PYLORI; HYDROGEN SULFITE; DERIVATIVES; DISULFIDES; ENZYME; ACID; AMINES;
D O I
10.1016/j.ejmech.2014.01.001
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Thiourea derivatives (1-38) were synthesized and evaluated for their urease inhibition potential. The synthetic compounds showed a varying degree of in vitro urease inhibition with IC50 values 5.53 +/- 0.02 -91.50 +/- 0.08 mu M, most of which are superior to the standard thiourea (IC(5)0 = 21.00 +/- 0.11 mu M). In order to ensure the mode of inhibition of these compounds, the kinetic study of the most active compounds has been carried out. Most of these inhibitors were found to be mixed-type of inhibitors, except compounds 13 and 30 which were competitive, while compound 19 was identified as non-competitive inhibitor with Ki values between 8.6 and 19.29 mu M. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:314 / 323
页数:10
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