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 …

[HTML][HTML] Synthesis, in vitro biological analysis and molecular docking studies of new thiadiazole-based thiourea derivatives as dual inhibitors of a-amylase and a …

I Khan, W Rehman, F Rahim, R Hussain, S Khan… - Arabian Journal of …, 2023 - Elsevier
Diabetes mellitus is a syndrome that is caused due to the imbalance of insulin production in
the body. In the present study we have synthesized a class of fifteen compounds (1–15) …

New thiazole-based thiazolidinone derivatives: synthesis, in vitro α-amylase, α-glucosidase activities and silico molecular docking study

S Khan, H Ullah, F Rahim, M Taha, R Hussain… - Chemical Data …, 2022 - Elsevier
A series of thiazole-based thiazolidinone derivatives (1-20) have been synthesized and
evaluated against α-glucosidase and α-amylase enzymes. All derivatives showed good α …

Design, synthesis, in silico testing, and in vitro evaluation of thiazolidinone-based benzothiazole derivatives as inhibitors of α-amylase and α-glucosidase

S Khan, S Iqbal, M Khan, W Rehman, M Shah… - Pharmaceuticals, 2022 - mdpi.com
In this study, a stepwise reaction afforded thiazolidinone-based benzothiazole derivatives 1–
15, and the synthesized derivatives were then screened for biological significance and …

Synthesis of novel benzimidazole-based thiazole derivatives as multipotent inhibitors of α-amylase and α-glucosidase: in vitro evaluation along with molecular …

R Hussain, S Iqbal, M Shah, W Rehman, S Khan… - Molecules, 2022 - mdpi.com
In this study, hybrid analogs of benzimidazole containing a thiazole moiety (1–17) were
afforded and then tested for their ability to inhibit α-amylase and α-glucosidase when …

Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives

KM Khan, S Qurban, U Salar, M Taha, S Hussain… - Bioorganic …, 2016 - Elsevier
Current study based on the synthesis of new thiazole derivatives via “one pot”
multicomponent reaction, evaluation of their in vitro α-glucosidase inhibitory activities, and in …

Synthesis, α-amylase inhibitory activity and molecular docking studies of 2, 4-thiazolidinedione derivatives

F Naeem, H Nadeem, A Muhammad… - Open Chemistry …, 2018 - benthamopen.com
Methods: All the synthesized compounds were characterized by elemental analysis, FTIR, 1
HNMR, and 13 CNMR and further screened for their α-amylase inhibitory potential. Results …

[HTML][HTML] New quinoline-based triazole hybrid analogs as effective inhibitors of α-amylase and α-glucosidase: Preparation, in vitro evaluation, and molecular docking …

Y Khan, S Iqbal, M Shah, A Maalik, R Hussain… - Frontiers in …, 2022 - frontiersin.org
The 7-quinolinyl bearing triazole analogues were synthesized (1-19) and according to
literature known protocol were screened in vitro for their α-amylase and α-glucosidase …

Syntheses, in vitro α-amylase and α-glucosidase dual inhibitory activities of 4-amino-1, 2, 4-triazole derivatives their molecular docking and kinetic studies

EO Yeye, KM Khan, S Chigurupati, A Wadood… - Bioorganic & medicinal …, 2020 - Elsevier
Abstract Thirty-three 4-amino-1, 2, 4-triazole derivatives 1–33 were synthesized by reacting
4-amino-1, 2, 4-triazole with a variety of benzaldehydes. The synthetic molecules were …

Synthesis, in vitro α-glucosidase and α-amylase activities and molecular docking study of oxadiazole-sulphonamide hybrid analogues

H Ullah, MW Aslam, F Rahim, A Hussain… - Chemical Data …, 2023 - Elsevier
Acarbose and voglibose are two different α-glucosidase and α-amylase inhibitors that are
used to manage diabetes mellitus. Sadly, these renowned and therapeutically effective …