[HTML][HTML] Therapeutic potential of 4-substituted coumarins: A conspectus

M Sharma, VK Vyas, S Bhatt, MD Ghate - European Journal of Medicinal …, 2022 - Elsevier
Substituted coumarins are a very large family of naturally occurring compounds, and
substituted coumarins are versatile scaffolds for the development of medicinally active …

Anti-Alzheimer activity of new coumarin-based derivatives targeting acetylcholinesterase inhibition

NN Kamel, HF Aly, GI Fouad, SS Abd El-Karim… - RSC …, 2023 - pubs.rsc.org
New 2-oxo-chromene-7-oxymethylene acetohydrazide derivatives 4a–d were designed and
synthesized with a variety of bioactive chemical fragments. The newly synthesized …

Chromenone: An emerging scaffold in anti-Alzheimer drug discovery

U Agarwal, S Verma, RK Tonk - Bioorganic & Medicinal Chemistry Letters, 2024 - Elsevier
Alzheimer's disease (AD) presents a growing global health concern. In recent decades,
natural and synthetic chromenone have emerged as promising drug candidates due to their …

Investigation of novel benzoxazole-oxadiazole derivatives as effective anti-Alzheimer's agents: in vitro and in silico approaches

S Anwar, W Rehman, R Hussain, S Khan, MM Alanazi… - Pharmaceuticals, 2023 - mdpi.com
Alzheimer's disease (AD) is a progressive neurological illness that is distinguished clinically
by cognitive and memory decline and adversely affects the people of old age. The …

Exploring target site interactions of 1, 3, 4-Oxadiazole/1, 3, 4-thiadiazole derivatives: Synthesis, characterization in vitro anti-urease and in silico molecular docking …

R Hussain, S Khan, W Rehman, Z Ullah, Y Khan… - Journal of Molecular …, 2025 - Elsevier
Urease enzyme is one of the major causes of severe health issues including urinary catheter
encrustation, gastric cancer, duodenal ulcer and peptic ulcer. In search for potent anti …

Molecular modeling, synthesis, and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory activities of novel benzimidazole-bearing thiadiazole derivatives

R Hussain, M Ashraf, S Khan, F Rahim… - Journal of Molecular …, 2024 - Elsevier
A new series of benzimidazole-based thiadiazole hybrids analogues (6a–p) as effective
Alzheimer's inhibitors were synthesized and then evaluated for their inhibition profile against …

Synthesis, biological evaluation, molecular docking, and MD simulation of novel 2, 4-disubstituted quinazoline derivatives as selective butyrylcholinesterase inhibitors …

S Sadeghian, R Razmi, S Khabnadideh… - Scientific Reports, 2024 - nature.com
Alzheimer's disease is the most prevalent neurodegenerative disorder characterized by
significant memory loss and cognitive impairments. Studies have shown that the expression …

[3+ 2] Cycloaddition Synthesis of New (Chromene‐1, 3, 4‐Oxadiazole) Hybrids Linked to Pyrazole Units as Potential Acetylcholinesterase Inhibitors

AAM Ahmed, AEM Mekky, SMH Sanad - ChemistrySelect, 2025 - Wiley Online Library
A lot of interest has been gained recently in develo** novel acetylcholinesterase (AChE)
inhibitors that can alleviate Alzheimer's symptoms. In the current study, we aimed to explore …

Some heterocycles connected to substituted piperazine by 1, 3, 4-oxadiazole linker: Design, synthesis, anticholinesterase and antioxidant activity

Z Kilic-Kurt, D Konyar, H Okur, A Kaplan… - Journal of Molecular …, 2025 - Elsevier
AD is a multifactorial neurodegenerative disease that has caused morbidity and mortality on
a global scale. Currently, there are only a few drugs used in the treatment of AD. Although …

Synthesis of anthraquinone-connected coumarin derivatives via grindstone method and their evaluation of antibacterial, antioxidant, tyrosinase inhibitory activities with …

V Loganathan, A Ahamed, S Radhakrishnan… - Heliyon, 2024 - cell.com
Anthraquinones and coumarins have excellent pharmacological activities and are an
important class of natural plant metabolites with various biological activities. In this study …