Synthetic α-glucosidase inhibitors as promising anti-diabetic agents: Recent developments and future challenges

A Mushtaq, U Azam, S Mehreen, MM Naseer - European journal of …, 2023 - Elsevier
Diabetes mellitus is one of the biggest challenges for the scientific community in the 21st
century. It is a well-recognized multifactorial health problem contributes significantly to high …

Recent developments in synthetic α-glucosidase inhibitors: A comprehensive review with structural and molecular insight

A Singh, K Singh, A Sharma, K Kaur, K Kaur… - Journal of Molecular …, 2023 - Elsevier
Diabetes mellitus is the prominent metabolic disorder affecting 422 million people around
the globe and cause severe associated problems like kidney disorders, heart and nervous …

Identification of 1, 3, 4-oxadiazolyl-containing β-carboline derivatives as novel α-glucosidase inhibitors with antidiabetic activity

D Xiao, L Lu, B Liang, Z Xiong, X Xu… - European Journal of …, 2023 - Elsevier
In this study, we designed and synthesized a novel class of 1, 3, 4-oxadiazolyl-containing β-
carboline derivatives, ie, compounds f1∼ f35 as potential α-glucosidase inhibitors. All the …

Synthesis, biological evaluation and action mechanism of 7H-[1, 2, 4] triazolo [3, 4-b][1, 3, 4] thiadiazine-phenylhydrazone derivatives as α-glucosidase inhibitors

Q Feng, J Zhang, S Luo, Y Huang, Z Peng… - European Journal of …, 2023 - Elsevier
In our work, several 7H-[1, 2, 4] triazolo [3, 4-b][1, 3, 4] thiadiazine-phenylhydrazone
derivatives as α-glucosidase inhibitors (α-GIs) were synthesized and characterized by 1 H …

Synthesis, in vitro, and in silico evaluation of Indazole Schiff bases as potential α-glucosidase inhibitors

S Shamim, KM Khan, N Ullah, M Mahdavi… - Journal of Molecular …, 2021 - Elsevier
Indazole Schiff bases were synthesized 1–24 and structurally characterized by different
spectroscopic techniques such as EI-MS, HREI-MS, 1 H-and 13 C-NMR. Stereochemistry of …

[HTML][HTML] Structural characterization and molecular docking screening of most potent 1, 2, 4-triazine sulfonamide derivatives as anti-cancer agents

S Mutahir, MA Khan, AM Naglah, MA Al-Omar… - Crystals, 2023 - mdpi.com
One of the biggest problems facing contemporary medicine is cancer. New approaches to
therapy are required due to the difficult and prolonged treatment, the numerous adverse …

Diphenyl-substituted triazine derivatives: synthesis, α-glucosidase inhibitory activity, kinetics and in silico studies

S Shamim, KM Khan, M Ali, M Mahdavi… - Future Medicinal …, 2023 - Taylor & Francis
Background: Diabetes mellitus (DM) is a chronic disorder, considered to be a major global
health challenge in the 21st century. α-Glucosidase enzyme is a well-known drug target to …

Design, synthesis and bio-evaluation of indolin-2-ones as potential antidiabetic agents

IG Asuquo, M Solangi, KM Khan… - Future Medicinal …, 2023 - Taylor & Francis
Background: Diabetes mellitus is a serious global health concern, and this is expected to
impact more than 300 million people by 2025. The current study focuses on identifying …

[HTML][HTML] Density functional theory (DFT), molecular docking, and xanthine oxidase inhibitory studies of dinaphthodiospyrol S from Diospyros kaki L

T Abu-Izneid, A Rauf, Z Ahmad, A Wadood… - Saudi Pharmaceutical …, 2024 - Elsevier
In this work, we investigated Diospyros kaki extract and an isolated compound for their
potential as xanthine oxidase (XO) inhibitors, a target enzyme involved in inflammatory …

Design, Synthesis and biological evaluation of novel benzopyran derivatives as potential α-amylase inhibitors: An Investigation by Experimental and Computational …

A Hajlaoui, A Assel, H Lazrag, J Bouajila… - Journal of Molecular …, 2023 - Elsevier
A novel series of benzopyran derivatives 4, 5, and 6a-i was synthesized via
cyclocondensation reaction of hydrazide 3 with some electrophilic species such as 2, 4 …