Pharmaceutical and medicinal significance of sulfur (SVI)-Containing motifs for drug discovery: A critical review

C Zhao, KP Rakesh, L Ravidar, WY Fang… - European journal of …, 2019 - Elsevier
Sulfur (S VI) based moieties, especially, the sulfonyl or sulfonamide based analogues have
showed a variety of pharmacological properties, and its derivatives propose a high degree …

Sulfonamide derivatives as multi-target agents for complex diseases

S Apaydın, M Török - Bioorganic & medicinal chemistry letters, 2019 - Elsevier
Sulfonamide derivatives are frequently seen structural motifs in medicinal chemistry. Almost
a century after Gerhard Domagk's pioneering work leading to the first sulfonamide antibiotic …

Synthesis, in vitro α-amylase, α-glucosidase activities and molecular docking study of new benzimidazole bearing thiazolidinone derivatives

S Khan, H Ullah, F Rahim, M Nawaz, R Hussain… - Journal of Molecular …, 2022 - Elsevier
We have synthesized a series of benzimidazole bearing thiazolidinone derivatives (1-20),
characterized through NMR and HREI-MS and screened against α-glucosidase and α …

Benzenesulfonamide derivatives as potent acetylcholinesterase, α-glycosidase, and glutathione S-transferase inhibitors: biological evaluation and molecular docking …

P Taslimi, M Işık, F Türkan, M Durgun… - Journal of …, 2021 - Taylor & Francis
Sulfonamide derivatives exhibit a wide biological activity and can function as potential
medical molecules in the development of a drug. Studies have reported that the compounds …

Discovery of imidazopyridine derived oxadiazole-based thiourea derivatives as potential anti-diabetic agents: Synthesis, in vitro antioxidant screening and in silico …

R Hussain, W Rehman, F Rahim, S Khan… - Journal of Molecular …, 2023 - Elsevier
A series of new imidazopyridine based oxadiazole derivatives (5a-l) were designed and
synthesized. Their structures were confirmed by spectral data and then subjected to in vitro …

Molecular docking and investigation of 4-(benzylideneamino)-and 4-(benzylamino)-benzenesulfonamide derivatives as potent AChE inhibitors

M Işık, Y Demir, M Durgun, C Türkeş, A Necip… - Chemical Papers, 2020 - Springer
The discovery of acetylcholinesterase inhibitors is important for the treatment of Alzheimer's
disease (AD), known as the most common type of dementia. Due to the side effects of …

Cross-Electrophile Coupling of Benzyl Halides and Disulfides Catalyzed by Iron

J Semenya, Y Yang, E Picazo - Journal of the American Chemical …, 2024 - ACS Publications
Cross-electrophile couplings are influential reactions that typically require a terminal
reductant or photoredox conditions. We discovered an iron-catalyzed reaction that couples …

Combined QSAR, molecular docking and molecular dynamics study on new Acetylcholinesterase and Butyrylcholinesterase inhibitors

I Daoud, N Melkemi, T Salah, S Ghalem - Computational biology and …, 2018 - Elsevier
Background and purpose This work deals with several molecular modeling methods used to
discover new therapeutic agents for treating the Alzheimer's disease (AD). The cholinergic …

[HTML][HTML] Experimental and computational pharmacological approaches decoding the anti-diabetic molecular mechanism of indole based triazole bearing …

S Khan, T Iqbal, Y Khan, R Hussain, MS Khan… - Results in …, 2024 - Elsevier
In search for a potent anti-Diabetes therapeutic agent, we have synthesized a series of
indole based triazole derived sulfonothioate derivatives (1–15). These compounds were …