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- W4308347924 abstract "• New thiadiazole were designed and synthesized. • Several functional groups were endured. • effective inhibitors of urease, glycation, and (DPPH) scavengers • Compound 13 was found as the effective and lead molecule • Molecular docking study was presented to explain numerous key binding interactions. Thiadiazole is a potential class of α-glucosidase, β -glucuronidase, and anti-leishmanial inhibitors. Our aim was to develop thiadiazole based dual inhibitors for urease glycation inhibition and (DDPH) scavenging activity. Pyridine-based-thiadiazole analogs ( 1-18 ) were synthesized and characterized through 1 H-NMR, 13 C-NMR, EI-HRMS. All synthesized compounds were new and showed good inhibition ranging between IC 50 value (0.70 ± 0.010 to 21.10 ± 0.90 μ M) when compared with standard thiourea (21.40 ± 0.21 μ M). Among the series, analog 13 having IC 50 value (0.70 ± 0.010) showed the most potent inhibition. All synthesized compounds screened for their antioxidant and antiglycation inhibitory effect, and they showed good inhibition for both. The binding interactions with urease enzyme with active inhibitors studied via molecular docking studies. The compound 13 showed potent urease, antiglycation and (DPPH) scavenging activity and showed its character as dual inhibitor." @default.
- W4308347924 created "2022-11-11" @default.
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- W4308347924 date "2023-02-01" @default.
- W4308347924 modified "2023-09-24" @default.
- W4308347924 title "Discovering biological efficacy of new thiadiazole as effective inhibitors of urease, glycation, and (DPPH) scavengers: Biochemical and in silico study" @default.
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- W4308347924 doi "https://doi.org/10.1016/j.molstruc.2022.134449" @default.
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