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• W3134097060 endingPage "130226" @default.
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• W3134097060 abstract "Involvement of urease in various pathological conditions specifically in gastric and peptic ulcers make it an important therapeutic target. In the present study urease inhibition was investigated by newly designed Schiff bases of levofloxacin. Structure elucidation of these compounds were done by spectral studies such as IR, 1H NMR and 13C NMR and elemental analysis. In vitro urease enzyme inhibition assay revealed the compounds LS01, LS06 and LS07 were found to be the most potent and showed comparable IC50 values 0.58±0.11, 0.45±0.21 µM and 0.52±0.28 µM respectively. The compound LS06 was competitive inhibitor with Ki value 1.13 µM while the compounds LS01 and LS07 were mixed type of inhibitors with Ki values 3.40 and 6.03 µM respectively. Plausible binding mode of competitive inhibitor was predicted using molecular docking studies. Ancillary to synthetic studies, density functional theory (DFT) at B3LYP/6–31G(d,p) basis sets in ground state is utilized in order to gain optimized geometries of LS01-LS09 molecules. Different geometric parameters like molecular electrostatic potential analysis, alignment of HOMO and LUMO levels, natural bonding orbital (NBO) analysis and global descriptor of reactivity were performed in support of experimental findings. All DFT based computed results showed best agreement with experimental finding and suggest that all synthesized compounds are chemically stable." @default.
• W3134097060 created "2021-03-15" @default.
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• W3134097060 date "2021-07-01" @default.
• W3134097060 modified "2023-10-15" @default.
• W3134097060 title "Levofloxacin and sulfa drugs linked via Schiff bases: Exploring their urease inhibition, enzyme kinetics and in silico studies" @default.
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• W3134097060 doi "https://doi.org/10.1016/j.molstruc.2021.130226" @default.
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