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The following term was not found in PubMed: 4-benzoxybenzyl
Page 1
Discovery of Novel Dihydropyrimidine and hydroxamic acid hybrids as potent Helicobacter pylori Urease inhibitors.
Mamidala R, Bhimathati SRS, Vema A. Mamidala R, et al. Bioorg Chem. 2021 Sep;114:105010. doi: 10.1016/j.bioorg.2021.105010. Epub 2021 May 28. Bioorg Chem. 2021. PMID: 34102519
In vitro enzyme inhibition screening led to the discovery of three potent urease inhibitors 2-[[4-(4-hydroxy phenyl)-6-oxo-1,6-dihydropyrimidine-2-yl]-amino]-N-hydroxy acetamide (4g), 2-[[4-(4-chloro phenyl)-6-oxo-1,6-dihydropyrimidine-2-yl]-amino]-N- …
In vitro enzyme inhibition screening led to the discovery of three potent urease inhibitors 2-[[4-(4-hydroxy phenyl)-6-oxo-1,6-dihydropyrimi …
Studies on the mechanism of acetamide hepatocarcinogenicity.
Dybing E, Søderlund EJ, Gordon WP, Holme JA, Christensen T, Becher G, Rivedal E, Thorgeirsson SS. Dybing E, et al. Pharmacol Toxicol. 1987 Jan;60(1):9-16. doi: 10.1111/j.1600-0773.1987.tb01712.x. Pharmacol Toxicol. 1987. PMID: 3550769
N-Hydroxy-acetamide was cytotoxic to monolayers of isolated hepatocytes at concentrations above 2.5 mM. This cytotoxicity was increased after diethyl maleate treatment, but N-hydroxy-acetamide did not deplete cellular glutathione. A HPLC
N-Hydroxy-acetamide was cytotoxic to monolayers of isolated hepatocytes at concentrations above 2.5 mM. This cytotoxici