2013
DOI: 10.4028/www.scientific.net/amr.746.40
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Synthesis and Structure Elucidation of Novel Oxime Ether Type H/K+-ATPase Inhibitors

Abstract: Six 6,6-dimethyl-2-phenyl-6,7-dihydrobenzofuran-4(5H)-one oxime derivatives were synthesized, characterized and evaluated as potential anti-ulcer agents. Most of the target compounds exhibited better H+/K+-ATPase inhibitory activity than commercial revaprazan, and both of the two O-propyl oxime ethers displayed the most potent activities with IC50˰̵̱̼͆̓ͅ˰̵̼̓̓˰̸̱̈́̾˰́̀˰μ̝˾ These compounds could be potentially used for the treatment of ulcer disease.

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“…The test compounds were dissolved in ethanol (initial concentration 10 mg/mL), and diluted with 1640 medium to different concentrations of 0~100 mg/L. The H + /K + -ATPase inhibitory activity was determined by H + /K + -ATPase kits according to our previous methods [10,11]. All data were presented as mean ± standard deviation and analyzed by SPSS.…”
Section: Synthesismentioning
confidence: 99%
“…The test compounds were dissolved in ethanol (initial concentration 10 mg/mL), and diluted with 1640 medium to different concentrations of 0~100 mg/L. The H + /K + -ATPase inhibitory activity was determined by H + /K + -ATPase kits according to our previous methods [10,11]. All data were presented as mean ± standard deviation and analyzed by SPSS.…”
Section: Synthesismentioning
confidence: 99%