3-Arylpropionylhydroxamic acid derivatives as Helicobacter pylori urease inhibitors: Synthesis, molecular docking and biological evaluation
Shi Wei-Kang
Deng Rui-Cheng
Wang Peng-Fei
Yue Qin-Qin
Liu Qi
Ding Kun-Ling
Yang Mei-Hui
Zhang Hong-Yu
Gong Si-Hua
Deng Min
Liu Wen-Run
Feng Qiu-Ju
Xiao Zhu-Ping
Zhu Hai-Liang
· 2016
3-arylpropionylhydroxamic酸
期刊名称:
Bioorganic and Medicinal Chemistry
2016 年
24 卷
19 期
摘要:
Helicobacter pylori urease is involved in several physiologic responses such as stomach and duodenal ulcers, adenocarcinomas and stomach lymphomas. Thus, inhibition of urease is taken for a good chance to treat H. pylori-caused infections, we have therefore focused our efforts on seeking novel urease inhibitors. Here, a series of arylpropionylhydroxamic acids were synthesized and evaluated for urease inhibition. Out of these compounds, 3-(2-benzyloxy-5-chlorophenyl)-3-hydroxypropionylhydroxamic acid (d24) was the most active inhibitor with IC