نتایج جستجو برای: galantamine

تعداد نتایج: 646  

Journal: :Health technology assessment 2001
A Clegg J Bryant T Nicholson L McIntyre S De Broe K Gerard N Waugh

BACKGROUND Alzheimer's disease is the most common cause of dementia and is characterised by an insidious onset and slow deterioration. The estimated prevalence of Alzheimer's disease for a standard health authority (500,000 people) is about 3330. Current service involves a wide range of agencies, and drug therapy for some patients. OBJECTIVES To provide a rapid and systematic review of the cl...

2013
Secundino López-Pousa Francisco Javier Arranz

BACKGROUND The aim of this study was to assess the sociodemographic and clinical characteristics of patients with Alzheimer's disease who switched from any oral cholinesterase inhibitor to rivastigmine patches. METHODS An observational, retrospective, multicenter study was conducted in patients with a diagnosis of Alzheimer's disease who had switched to rivastigmine patches within the previou...

Journal: :Cochrane Database of Systematic Reviews 2009

Journal: :Trends in Sciences 2022

Alzheimer’s disease (AD) is a major public health problem worldwide due to an increase in the elderly population. The current pharmacotherapy for early stages of AD mainly dependent on cholinesterase inhibitors. Two most commonly used anti-AD drugs, donepezil (DPZ) and galantamine (GLM), are selective inhibitors human acetylcholinesterase (hAChE). However, inhibitory activity DPZ hAChE was more...

Journal: :Molecules 2012
Pedro de la Torre Luis Astudillo Saavedra Julio Caballero Jairo Quiroga Jans H Alzate-Morales Margarita Gutiérrez Cabrera Jorge Trilleras

(E)-2-(benzo[d]thiazol-2-yl)-3-heteroarylacrylonitriles are described as a new class of selective inhibitors of acetylcholinesterase (AChE). The most potent compound in the series exhibited good AChE inhibitory activity (IC₅₀ = 64 µM). Compound 7f was found to be more selective than galanthamine in inhibiting AChE and it showed a moderate selectivity index. Kinetic studies on AChE indicated tha...

Journal: :Journal of the American Chemical Society 2004
Harry M Greenblatt Catherine Guillou Daniel Guénard Anat Argaman Simone Botti Bernard Badet Claude Thal Israel Silman Joel L Sussman

Bifunctional derivatives of the alkaloid galanthamine, designed to interact with both the active site of the enzyme acetylcholinesterase (AChE) and its peripheral cation binding site, have been assayed with Torpedo californica AChE (TcAChE), and the three-dimensional structures of their complexes with the enzyme have been solved by X-ray crystallography. Differences were noted between the IC(50...

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