Molecular docking, chemo-informatic properties, alpha-amylase, and lipase inhibition studies of benzodioxol derivatives

M Hawash, N Jaradat, S Shekfeh, M Abualhasan… - BMC chemistry, 2021 - Springer
Currently, available therapies for diabetes could not achieve normal sugar values in a high
percentage of treated patients. In this research project, a series of 17 benzodioxole …

In silico design of new α-glucosidase inhibitors through 3D-QSAR study, molecular docking modeling and ADMET analysis

A Khaldan, S Bouamrane, REMA Ajana… - Moroccan Journal of …, 2022 - revues.imist.ma
Abstract α-Glucosidase enzyme is a therapeutic target for diabetes mellitus and its inhibitors
shown a crucial importance in the treatment of this disease. Twenty oxindole based …

2, 4-Dichloro-5-[(N-aryl/alkyl) sulfamoyl] benzoic acid derivatives: in vitro antidiabetic activity, molecular modeling and in silico ADMET screening

S Thakral, V Singh - Medicinal Chemistry, 2019 - ingentaconnect.com
Background: Postprandial hyperglycemia can be reduced by inhibiting major carbohydrate
hydrolyzing enzymes, such as α-glucosidase and α-amylase which is an effective approach …

[HTML][HTML] Aryl-oxadiazole Schiff bases: Synthesis, α-glucosidase in vitro inhibitory activity and their in silico studies

H Ullah, F Rahim, M Taha, R Hussain… - Arabian Journal of …, 2020 - Elsevier
Abstract α-Glucosidase enzyme is a therapeutic target for diabetes mellitus and its inhibitors
play a vital role in the treatment of this disease. A new series of aryl-oxadiazole Schiff bases …

Biological, toxicological and molecular docking evaluations of isoxazoline-thiazolidine-2, 4-dione analogues as new class of anti-hyperglycemic agents

S Fettach, FZ Thari, Z Hafidi, K Karrouchi… - Journal of …, 2023 - Taylor & Francis
In this work, three isoxazoline-thiazolidine-2, 4-dione derivatives were synthesized and
characterized by FT-IR, 1H-NMR, 13C-NMR and ESI-MS spectrometry. All compounds have …

Synthesis, biological evaluation and molecular docking study of benzimidazole derivatives as α-glucosidase inhibitors and anti-diabetes candidates

S Hayat, H Ullah, F Rahim, I Ullah, M Taha… - Journal of Molecular …, 2023 - Elsevier
Voglibose and acarbose are distinguished α-glucosidase inhibitors used for controlling
diabetes mellitus. Unfortunately, these distinguished and clinically used inhibitors have also …

Synthesis of triazinoindole bearing sulfonamide derivatives, in vitro α-amylase activity and their molecular docking study

H Zada, H Ullah, S Hayat, F Rahim, F Khan… - Chemical Data …, 2022 - Elsevier
Diabetes mellitus is one of the most chronic metabolic diseases. Since past few years, our
research group had synthesized and evaluated libraries of heterocyclic analogues against α …

Synthesis, molecular docking study of thiazole derivatives and exploring their dual inhibitor potentials against α-amylase and α-glucosidase

H Ullah, N Ahmad, F Rahim, I Uddin, S Hayat… - Chemical Data …, 2022 - Elsevier
Diabetes mellitus is one of the most chronic metabolic diseases. The current study
comprises of evaluation of thiazole as an antidiabetic agent. A library of sixteen derivatives …

Synthesis of indole derivatives as diabetics II inhibitors and enzymatic kinetics study of α-glucosidase and α-amylase along with their in-silico study

M Taha, AS Alrashedy, NB Almandil, N Iqbal… - International Journal of …, 2021 - Elsevier
In this study, we have investigated a series of indole-based compounds for their inhibitory
study against pancreatic α-amylase and intestinal α-glucosidase activity. Inhibitors of …

Identification of potential N-substituted 5-benzylidenethiazolidine-2, 4‑dione derivatives as α-amylase inhibitors: Computational cum synthetic studies

S Gupta, GS Baweja, GD Gupta, V Asati - Journal of Molecular Structure, 2023 - Elsevier
Diabetes mellitus is a chronic metabolic disorder become a major health problem globally
associated with social and economic consequences. α-amylase is an endo-amylase …