New acetylcholinesterase inhibitors for alzheimer's disease
Document Type
Article
Abstract
Acetylcholinesterase (AChE) remains a highly viable target for the symptomatic improvement in Alzheimer's disease (AD) because cholinergic deficit is a consistent and early finding in AD. The treatment approach of inhibiting peripheral AchE for myasthenia gravis had effectively proven that AchE inhibition was a reachable therapeutic target. Subsequently tacrine, donepezil, rivastigmine, and galantamine were developed and approved for the symptomatic treatment of AD. Since then, multiple cholinesterase inhibitors (ChEI) continue to be developed. These include newer ChEIs, naturally derived ChEIs, hybrids, and synthetic analogues. In this paper, we summarize the different types of ChEIs in development and their respective mechanisms of actions. This pharmacological approach continues to be active with many promising compounds. © 2012 Mona Mehta et al.
Publication Date
1-12-2012
Publication Title
International Journal of Alzheimer's Disease
E-ISSN
20900252
Digital Object Identifier (DOI)
10.1155/2012/728983
Recommended Citation
Mehta, Mona; Adem, Abdu; and Sabbagh, Marwan, "New acetylcholinesterase inhibitors for alzheimer's disease" (2012). Neurology. 959.
https://scholar.barrowneuro.org/neurology/959