Synthetic approaches and pharmaceutical applications of chloro-containing molecules for drug discovery: A critical review

WY Fang, L Ravindar, KP Rakesh… - European Journal of …, 2019 - Elsevier
At present more than 250 FDA approved chlorine containing drugs were available in the
market and many pharmaceutically important drug candidates in pre-clinical trials. Thus, it is …

An insight of alpha-amylase inhibitors as a valuable tool in the management of type 2 diabetes mellitus

R Bashary, M Vyas, SK Nayak, A Suttee… - Current diabetes …, 2020 - benthamdirect.com
Background: Among the millions of people around the world, the most prevalent metabolic
disorder is diabetes mellitus. Due to the drawbacks which are associated with commercially …

Molecular docking, ADME-Tox, DFT and molecular dynamics simulation of butyroyl glucopyranoside derivatives against DNA gyrase inhibitors as antimicrobial agents

N Akter, L Bourougaa, M Ouassaf, RC Bhowmic… - Journal of Molecular …, 2024 - Elsevier
The emergence of antibiotic resistance highlights the critical need for novel antimicrobial
agents. In this study, we investigated the synthesis of methyl α-D-glucopyranoside (1) …

Synthesis, characterization, molecular docking, and biological activities of coumarin–1, 2, 3‐triazole‐acetamide hybrid derivatives

N Sepehri, M Mohammadi‐Khanaposhtani… - Archiv der …, 2020 - Wiley Online Library
Coumarins and their derivatives are receiving increasing attention due to numerous
biochemical and pharmacological applications. In this study, a series of novel coumarin–1 …

[HTML][HTML] New benzoxazole-based sulphonamide hybrids analogs as potent inhibitors of α-amylase and α-glucosidase: Synthesis and in vitro evaluation along with in …

S Khan, F Rahim, W Rehman, M Nawaz, M Taha… - Arabian Journal of …, 2022 - Elsevier
The development of drugs resistance in diabetes mellitus is a growing clinical problem,
creates many challenges for patient. To overcome these problems, there is a serious …

Synthesis and biological evaluation of new benzimidazole-1, 2, 3-triazole hybrids as potential α-glucosidase inhibitors

N Asemanipoor, M Mohammadi-Khanaposhtani… - Bioorganic …, 2020 - Elsevier
In this study, a series of benzimidazole-1, 2, 3-triazole hybrids 8a-n as new α-glucosidase
inhibitors were designed and synthesized. In vitro α-glucosidase inhibition activity results …

Exploring indole-based-thiadiazole derivatives as potent acetylcholinesterase and butyrylcholinesterase enzyme inhibitors

M Taha, F Rahim, N Uddin, IU Khan, N Iqbal… - International Journal of …, 2021 - Elsevier
Abstract Indole based thiadiazole derivatives (1–18) were synthesized and evaluated for
their acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibition. The IC 50 …

Synthesis of new indazole based dual inhibitors of α-glucosidase and α-amylase enzymes, their in vitro, in silico and kinetics studies

R Rafique, KM Khan, S Chigurupati, A Wadood… - Bioorganic …, 2020 - Elsevier
The current study describes the discovery of novel inhibitors of α-glucosidase and α-
amylase enzymes. For that purpose, new hybrid analogs of N-hydrazinecarbothioamide …

Indole-nitroimidazole conjugates as efficient manipulators to decrease the genes expression of methicillin-resistant Staphylococcus aureus

ZZ Li, VKR Tangadanchu, N Battini… - European Journal of …, 2019 - Elsevier
The biological resistance of methicillin-resistant staphylococcus aureus (MRSA) has pushed
synthetic antibiotics to the forefront. To combat the resistance of MRSA, our new effort …