Thiazole: A versatile standalone moiety contributing to the development of various drugs and biologically active agents

MF Arshad, A Alam, AA Alshammari, MB Alhazza… - Molecules, 2022 - mdpi.com
For many decades, the thiazole moiety has been an important heterocycle in the world of
chemistry. The thiazole ring consists of sulfur and nitrogen in such a fashion that the pi (π) …

Inhibitory potential of nitrogen, oxygen and sulfur containing heterocyclic scaffolds against acetylcholinesterase and butyrylcholinesterase

RJ Obaid, N Naeem, EU Mughal, MM Al-Rooqi… - RSC …, 2022 - pubs.rsc.org
Heterocycles are the key structures in organic chemistry owing to their immense applications
in the biological, chemical, and pharmaceutical fields. Heterocyclic compounds perform …

Coumarin linked heterocyclic hybrids: a promising approach to develop multi target drugs for Alzheimer's disease

A Husain, K Al Balushi, MJ Akhtar, SA Khan - Journal of Molecular Structure, 2021 - Elsevier
Alzheimer's disease (AD) is a major progressive and perplexing cortical degenerative
disease of the brain in the elderly. It contributes to a significant socioeconomic burden on …

[HTML][HTML] Recent advancements in the synthesis of fused thienopyridines and their therapeutic applications

R Shaw, R Tewari, M Yadav, E Pandey… - European Journal of …, 2024 - Elsevier
Fused thienopyridines represent a class of heterocyclic molecules that have garnered
increasing attention due to their unique structural features and versatile chemical properties …

Hybrid quinoline-thiosemicarbazone therapeutics as a new treatment opportunity for Alzheimer's disease‒synthesis, in vitro cholinesterase inhibitory potential and …

S Zaib, R Munir, MT Younas, N Kausar, A Ibrar, S Aqsa… - Molecules, 2021 - mdpi.com
Alzheimer's disease (AD) is a progressive neurodegenerative disorder and the leading
cause of dementia worldwide. The limited pharmacological approaches based on …

[HTML][HTML] In vitro and in silico evaluation of the antimicrobial and antioxidant activities of spiropyrazoline oxindole congeners

M Chalkha, K Chebbac, H Nour, A Nakkabi… - Arabian Journal of …, 2024 - Elsevier
The search for novel powerful antimicrobial and antioxidant agents is considered a dynamic
field in medicinal chemistry. In this context, a series of spiropyrazoline indolin-3-one …

Citronellal as a promising candidate for Alzheimer's disease treatment: A comprehensive study on in silico and in vivo anti-acetylcholine esterase activity

DS Prasanth, MKR Shadakshara, SF Ahmad… - Metabolites, 2023 - mdpi.com
One of the primary therapeutic approaches for managing Alzheimer's disease (AD) involves
the modulation of Acetylcholine esterase (AChE) activity to elevate acetylcholine (ACh) …

New thiazole and thiazole-chromene hybrids possessing morpholine units: Piperazine-mediated one-pot synthesis of potential acetylcholinesterase inhibitors

AEM Mekky, SMH Sanad… - Synthetic Communications, 2021 - Taylor & Francis
In the current study, new morpholine-linked thiazoles were prepared by the reaction of
salicylaldehyde derivative, thiosemicarbazide, and α-bromoketones. To mediate the …

Exploring biological efficacy of coumarin clubbed thiazolo [3, 2–b][1, 2, 4] triazoles as efficient inhibitors of urease: A biochemical and in silico approach

I Khan, A Khan, SA Halim, A Saeed, S Mehsud… - International journal of …, 2020 - Elsevier
Combating several pathological conditions associated with ureolytic enzyme (urease)
remains a formidable challenge because of the lack of effective and safe drug therapies. In …

Synthesis and biological evaluation of 2-nitrocinnamaldehyde derived thiosemicarbazones as urease inhibitors

M Islam, A Khan, M Khan, SA Halim, S Ullah… - Journal of Molecular …, 2023 - Elsevier
Hyperactivity of urease enzyme induces pathogenesis of peptic ulcers and gastritis. The
excess of urease can be reduced by introducing various inhibitors. The risk of high urease …