Title : Structure-activity relationship studies of benzyl-, phenethyl-, and pyridyl-substituted tetrahydroacridin-9-amines as multitargeting agents to treat Alzheimer's disease.

Pub. Date : 2016 Nov

PMID : 27282589






1 Functional Relationships(s)
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1 The picolylamine-substituted compound 12c (6-chloro-N-(pyridin-2-ylmethyl)-1,2,3,4-tetrahydroacridin-9-amine) was the most potent AChE inhibitor (IC50 = 90 nm). 6-chloro-n-(pyridin-2-ylmethyl)-1,2,3,4-tetrahydroacridin-9-amine acetylcholinesterase (Cartwright blood group) Homo sapiens