Recent advance on carbamate-based cholinesterase inhibitors as potential multifunctional agents against Alzheimer's disease
Abstract Alzheimer's disease (AD), as the fourth leading cause of death among the elderly
worldwide, has brought enormous challenge to the society. Due to its extremely complex …
worldwide, has brought enormous challenge to the society. Due to its extremely complex …
Pathogenesis of Alzheimer's Disease and Diversity of 1, 2, 3-Triazole Scaffold in Drug Development: Design Strategies, Structural Insights, and Therapeutic Potential
Alzheimer's disease is a most prevalent form of dementia all around the globe and currently
poses a significant challenge to the healthcare system. Currently available drugs only slow …
poses a significant challenge to the healthcare system. Currently available drugs only slow …
Progress in target drug molecules for Alzheimer's disease
J Xie, R Liang, Y Wang, J Huang… - Current Topics in …, 2020 - ingentaconnect.com
Alzheimer's disease (AD) is a chronic neurodegenerative disease that 4 widespread in the
elderly. The etiology of AD is complicated, and its pathogenesis is still unclear. Although …
elderly. The etiology of AD is complicated, and its pathogenesis is still unclear. Although …
Contemporary medicinal-chemistry strategies for the discovery of selective butyrylcholinesterase inhibitors
L Jing, G Wu, D Kang, Z Zhou, Y Song, X Liu… - Drug discovery today, 2019 - Elsevier
Highlights•BChE is considered a promising drug target for the treatment of moderate to
severe Alzheimer's disease.•The development of selective BChE inhibitors will move on …
severe Alzheimer's disease.•The development of selective BChE inhibitors will move on …
Thiadiazole carbamates: potent inhibitors of lysosomal acid lipase and potential Niemann− Pick type C disease therapeutics
AI Rosenbaum, CC Cosner, CJ Mariani… - Journal of medicinal …, 2010 - ACS Publications
Niemann− Pick type C (NPC) disease is a lysosomal storage disorder characterized at the
cellular level by abnormal accumulation of cholesterol and other lipids in lysosomal storage …
cellular level by abnormal accumulation of cholesterol and other lipids in lysosomal storage …
Design, synthesis, biological evaluation, and molecular modeling studies of chalcone-rivastigmine hybrids as cholinesterase inhibitors
A series of novel chalcone-rivastigmine hybrids were designed, synthesized, and tested in
vitro for their ability to inhibit human acetylcholinesterase and butyrylcholinesterase. Most of …
vitro for their ability to inhibit human acetylcholinesterase and butyrylcholinesterase. Most of …
Solvents and detergents compatible with enzyme kinetic studies of cholinesterases
Abstract Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) are enzymes that
serve a wide range of physiological functions including the hydrolysis of the neurotransmitter …
serve a wide range of physiological functions including the hydrolysis of the neurotransmitter …
Isosorbide-2-benzyl carbamate-5-salicylate, a peripheral anionic site binding subnanomolar selective butyrylcholinesterase inhibitor
CG Carolan, GP Dillon, D Khan, SA Ryder… - Journal of medicinal …, 2010 - ACS Publications
Isosorbide-2-benzyl carbamate-5-benzoate is a highly potent and selective BuChE inhibitor.
Meanwhile, isosorbide-2-aspirinate-5-salicylate is a highly effective aspirin prodrug that …
Meanwhile, isosorbide-2-aspirinate-5-salicylate is a highly effective aspirin prodrug that …
Expansion of the scaffold diversity for the development of highly selective butyrylcholinesterase (BChE) inhibitors: Discovery of new hits through the pharmacophore …
X Lu, H Yang, Q Li, Y Chen, Q Li, Y Zhou, F Feng… - Bioorganic …, 2019 - Elsevier
Butyrylcholinesterase (BChE) is recently considered as a new target for the treatment of
Alzheimer's disease (AD). There is an increasing interest in the development of BChE …
Alzheimer's disease (AD). There is an increasing interest in the development of BChE …
Dual inhibition of the α-glucosidase and butyrylcholinesterase studied by Molecular Field Topology Analysis
F Jabeen, PV Oliferenko, AA Oliferenko… - European Journal of …, 2014 - Elsevier
A striking dual inhibition of enzymes α-glucosidase and butyrylcholinesterase by small drug-
like molecules, including 1, 4-disubstituted-1, 2, 3-triazoles, chalcones, and …
like molecules, including 1, 4-disubstituted-1, 2, 3-triazoles, chalcones, and …