… Efficient synthesis of unsubstituted hydroxamic acids is challenging, in part due to the
hydrolytic sensitivity of many such products. (48, 49) In light of this and of the low accessibility of …

… had the highest amylase inhibition (29.6 ± … synthesized CuO NPs and plant extracts were
also tested to compare and contrast their urease inhibition potency whereas a standard inhibitor…

… its ability to overcome inhibition by either synthesis of more … kinetics researchers of modern
era prefer enzyme inhibitor … offers an environment for Helicobacter pylori colonization and …

… Saleem et al., “Synthesis, urease Inhibition, antioxidant, antibacterial, and molecular docking
studies of 1, 3, 4-oxadiazole derivatives,” ISRN Pharmacology, vol. 2012, Article ID 928901, …

… urease inhibition, our results are in line with those previously reported, wherein potent urease
… In addition, enzyme kinetic studies may reveal the underlying mechanism of action of the …

… Besides, molecular docking simulation suggested the key … The structural features of the
synthetic compounds were all … the COX-2 inhibition and the anti-tumor effect. Additionally, …

… Synthesis, molecular docking and kinetic properties of β-hydroxyβ-phenylpropionyl-hydroxamic
acids as Helicobacter pylori urease inhibitors,” European Journal of Medicinal Chemistry…