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 …

Current anti-diabetic agents and their molecular targets: A review

N Kerru, A Singh-Pillay, P Awolade, P Singh - European Journal of …, 2018 - Elsevier
Diabetes mellitus is a medical condition characterized by the body's loss of control over
blood sugar. The frequency of diagnosed cases and consequential increases in medical …

Synthesis, DFT studies, molecular docking and biological activity evaluation of thiazole-sulfonamide derivatives as potent Alzheimer's inhibitors

S Khan, H Ullah, M Taha, F Rahim, M Sarfraz, R Iqbal… - Molecules, 2023 - mdpi.com
Alzheimer's disease is a major public brain condition that has resulted in many deaths, as
revealed by the World Health Organization (WHO). Conventional Alzheimer's treatments …

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, characterization, and inhibition study of novel substituted phenylureido sulfaguanidine derivatives as α‐glycosidase and cholinesterase inhibitors

S Akocak, P Taslimi, N Lolak, M Işık… - Chemistry & …, 2021 - Wiley Online Library
A series of six N‐carbamimidoyl‐4‐(3‐substituted phenylureido) benzenesulfonamide
derivatives were synthesized by reaction of sulfaguanidine with aromatic isocyanates. In …

Novel bis-ureido-substituted sulfaguanidines and sulfisoxazoles as carbonic anhydrase and acetylcholinesterase inhibitors

N Lolak, S Akocak, M Durgun, HE Duran, A Necip… - Molecular Diversity, 2023 - Springer
To discover alternative substances to compounds used to treat many diseases, especially
treating Alzheimer's disease (AD) and Parkinson's disease targeting carbonic anhydrase (h …

Design, Synthesis, and Antimicrobial Evaluation of a New Series of N-Sulfonamide 2-Pyridones as Dual Inhibitors of DHPS and DHFR Enzymes

RA Azzam, RE Elsayed, GH Elgemeie - ACS omega, 2020 - ACS Publications
Sulfonamides and trimethoprim (TMP) drugs are normally used to inhibit the action of
dihydropteroate synthase (DHPS) and dihydrofolate reductase (DHFR) enzymes …

Sulfa drug analogs: new classes of N-sulfonyl aminated azines and their biological and preclinical importance in medicinal chemistry (2000–2018)

GH Elgemeie, RA Azzam, RE Elsayed - Medicinal Chemistry Research, 2019 - Springer
N-sulfonylamino azinones has attracted the interest of numerous researchers and extensive
investigations on their biological activities have been done. The present review provides an …

Synthesis, anticancer and antitubercular properties of new chalcones and their nitrogen-containing five-membered heterocyclic hybrids bearing sulfonamide moiety

LF Castaño, J Quiroga, R Abonia, D Insuasty… - International Journal of …, 2022 - mdpi.com
A new series of sulfonamides, 8a-b, 10, 12, and 14a-b, were synthesized by N-sulfonation
reaction with sulfonyl chlorides 6a-b. Five new series of chalcone-sulfonamide hybrids (16 …

Recent advances in biological active sulfonamide based hybrid compounds Part A: Two-component sulfonamide hybrids

R Ghomashi, S Ghomashi, H Aghaei… - Current Medicinal …, 2023 - ingentaconnect.com
Sulfonamides constitute an important class of drugs, with many types of pharmacological
agents possessing antibacterial, anti-carbonic anhydrase, anti-obesity, diuretic …