| Literature DB >> 21216144 |
Ziyad F Al-Rashid1, Richard P Hsung.
Abstract
A computation docking study of the highly potent, non-nitrogen containing, acetylcholinesterase inhibitor (+)-arisugacin A is presented. The model suggests that (+)-arisugacin A is a dual binding site covalent inhibitor of AChE. These findings are examined in the context of Alzheimer's disease-modifying therapeutic design. (+)-Arisugacin A's revealed mode of action is unique, and may serve as a basis for the development of AD therapeutics capable of treating the symptomatic aspects of AD, while being neuroprotective with long term efficacy.Entities:
Mesh:
Substances:
Year: 2010 PMID: 21216144 PMCID: PMC3082004 DOI: 10.1016/j.bmcl.2010.12.041
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823