Aug 2026· Medicinal Chemistry Research· Vol 35, pp. 1801 - 1818· 0 citations· 43 references
Medicine
TL;DR
Compound 17v represents a promising lead compound for anti-Alzheimer's therapy and may possess multi-target neuroprotective potential and a favorable preliminary safety profile, supporting its further investigation as a potential therapeutic candidate for Alzheimer’s disease.
Findings identify trimetazidine‐derived hydrazide‐hydrazones as a promising chemotype for the development of selective AChE inhibitors and provide a basis for further optimization and advanced biological validation.
Muhammed Oğuzhan Doğan, B. Özkan, A. B. Karaduman et al.· Drug development research (P...· 0 citations
Several synthesized spiropyrrolidine compounds exhibited favorable binding interactions with key active site residues and showed promising drug-like properties, which may serve as potential leads for the development of novel AChE inhibitors and may provide new insights for therapeutic strategies in Alzheimer's disease.
Paranthaman Shamala, Mohamed Noor Shaik, P. B. et al.· Research journal of biotechn...· 0 citations
Interestingly, compounds 7a and 8a exhibited five‐fold higher selectivity for BChE than AChE, suggesting their potential relevance for further exploration in the context of Alzheimer's disease therapeutics.
Dilan Konyar, Hayati Okur, M. T. Muhammed et al.· ChemistrySelect· 0 citations
AIM
To synthesize novel sulfonohydrazide derivatives and evaluate their physicochemical and enzyme‑inhibitory profiles, together with the corresponding structure-activity relationships.
METHODS
A series of six hydrazide derivatives (NLs1-NLs6) was synthesized and subjected to comprehensive in vitro enzymatic evaluati...
Lubabah Abdul Karim, Amara Mumtaz, S. Ejaz et al.· Future Medicinal Chemistry· 0 citations
Alzheimer’s disease (AD), involves progressive cognitive impairment primarily associated with cholinergic dysfunction. Dual inhibition of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) continue to represent a validated and clinically relevant therapeutic approach for alleviating cholinergic deficits in...
Y. Khan, Hina Sarfraz, Azmatullah Khan et al.· Journal of Computational Bio...· 0 citations
Together with their dual cholinesterase inhibitory activities, compounds 6a and 6c represent promising multifunctional in vitro lead candidates for further development against neurodegenerative disorders associated with neurodegenerative disorders associated with neuroinflammation and oxidative stress.
Amina Hussain, Rafaqat Hussain, Hina Sarfraz et al.· Journal of Computer-Aided Mo...· 0 citations
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