We described here our results on the use of thiourea as a ligand in the copper catalysed
azide‐alkyne cycloaddition (CuAAC) of 2‐azidobenzaldehyde with alkynes. Reactions were …

A novel series of 2-pyrazoline derivatives were designed, synthesized, and evaluated for
cholinesterase (ChE) inhibitory, Aβ anti-aggregating and neuroprotective activities. Among …

In this study, four series of compounds with benzoxazolone and benzothiazolone cores were
designed, synthesized and evaluated as multifunctional agents against Alzheimer's disease …

In this study, a series of new benzimidazole/1, 3, 5-triazine-2, 4-diamine hybrid derivatives
(9a–9l) were designed and synthesized. The potential multi-target profiles of these …

In our overall goal to overcome the limitations associated with natural products for the
management of Alzheimer's disease and to develop in-vivo active multifunctional cholinergic …

The diverse nature of Alzheimer's disease (AD) has prompted researchers to develop multi-
functional agents. Herein, we have designed and synthesized molecular hybrids of 2 …

Inspite of established symptomatic relief drug targets, a multi targeting approach is highly in
demand to cure Alzheimer's disease (AD). Simultaneous inhibition of cholinesterase (ChE) …

Abstract A series of 2-acetyl-5-O-(amino-alkyl) phenol derivatives was designed,
synthesized and evaluated as multi-function inhibitors for the treatment of Alzheimer's …

In our endeavor towards the development of potent multitarget ligands for the treatment of
Alzheimer's disease, a series of triazine-triazolopyrimidine hybrids were designed …

Multitargeted hybrids of N-benzylpiperidine and substituted 5-phenyl-1, 3, 4-oxadiazoles
were designed, synthesized, and evaluated against Alzheimer's disease (AD). Tested …