The putative neurodegenerative links between depression and Alzheimer's disease
Alzheimer's disease (AD) is the leading neurodegenerative cause of dementia in the elderly.
Thus far, there is no curative treatment for this devastating condition, thereby creating …
Thus far, there is no curative treatment for this devastating condition, thereby creating …
Recent progress in the development of synthetic hybrids of natural or unnatural bioactive compounds for medicinal chemistry
SB Tsogoeva - Mini reviews in medicinal chemistry, 2010 - ingentaconnect.com
The present mini-review highlights the recent developments on different classes of synthetic
hybrids of natural and/or unnatural bioactive compounds, the utilization of which is very …
hybrids of natural and/or unnatural bioactive compounds, the utilization of which is very …
Acetylcholinesterase and butyrylcholinesterase inhibitory activity of some selected Nigerian medicinal plants
TO Elufioye, EM Obuotor, AT Sennuga… - Revista Brasileira de …, 2010 - SciELO Brasil
Plants have been found to be useful as memory enhansers as well as antiaging. Twenty two
of such plants from sixteen families were investigated for their acetylcholinesterase (AChE) …
of such plants from sixteen families were investigated for their acetylcholinesterase (AChE) …
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 …
4-Phenylcoumarins from Mesua elegans with acetylcholinesterase inhibitory activity
A significant acetylcholinesterase (AChE) inhibitory activity was observed for the hexane
extract from the bark of Mesua elegans (Clusiaceae). Thus, the hexane extract was …
extract from the bark of Mesua elegans (Clusiaceae). Thus, the hexane extract was …
From Anti-Allergic to Anti-Alzheimer's: Molecular Pharmacology of Dimebon™
I Okun, SE Tkachenko, A Khvat, O Mitkin… - Current Alzheimer …, 2010 - ingentaconnect.com
Dimebon, originally developed as an anti-histamine drug, is being re-purposed for new
indications as an effective treatment for patients suffering from Alzheimer's and Huntington's …
indications as an effective treatment for patients suffering from Alzheimer's and Huntington's …
Structural determinants of the multifunctional profile of dual binding site acetylcholinesterase inhibitors as anti-Alzheimer agents
C Galdeano, E Viayna, P Arroyo… - Current …, 2010 - ingentaconnect.com
Dual binding site acetylcholinesterase inhibitors have recently emerged as a new class of
anti-Alzheimer agents with potential to positively modify the course of the disease. These …
anti-Alzheimer agents with potential to positively modify the course of the disease. These …
Safety and tolerability of transdermal and oral rivastigmine in Alzheimer's disease and Parkinson's disease dementia
T Darreh-Shori, V Jelic - Expert Opinion on Drug Safety, 2010 - Taylor & Francis
Importance of the field: Cholinesterase inhibitors are the mainstay of symptomatic therapy for
Alzheimer's disease (AD). Rivastigmine, an inhibitor of both acetylcholinesterase and …
Alzheimer's disease (AD). Rivastigmine, an inhibitor of both acetylcholinesterase and …
Drug profile: transdermal rivastigmine patch in the treatment of Alzheimer disease
M Emre, R Bernabei, R Blesa, R Bullock… - CNS neuroscience & …, 2010 - Wiley Online Library
Cholinesterase inhibitors constitute one of the mainstays of treatment of Alzheimer disease
(AD). Gastrointestinal side effects, difficulty accessing therapeutic doses and poor patient …
(AD). Gastrointestinal side effects, difficulty accessing therapeutic doses and poor patient …
胆碱酯酶抑制剂(S)-卡巴拉汀及其类似物的不对称合成与活性研究
徐刚, 文富华, 买小胖, 孙平华, 黄美燕, 陈卫民 - 有机化学, 2010 - sioc-journal.cn
以对羟基苯甲醛或间羟基苯甲醛为原料, 用(R) 或(S)-叔丁基亚磺酰胺为手性引发剂,
设计合成了(S)-卡巴拉汀及其12 个未见文献报道的类似物, 其结构通过IR, 1 H NMR, 13 C NMR …
设计合成了(S)-卡巴拉汀及其12 个未见文献报道的类似物, 其结构通过IR, 1 H NMR, 13 C NMR …