The S and R isomers of p-methoxytacripyrine, a recently developed multi-target-directed agent for the treatment of Alzheimer's disease, were investigated. The S enantiomer has emerged as a new promising drug candidate inhibiting cholinesterase activity, amyloid aggregation and showing significant neuroprotective properties against Aβ25–35-induced cytotoxicity.
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Bartolini et al. (2011) studied this question.
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