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Bioorganic and Medicinal Chemistry 2005-Jul

New selective acetylcholinesterase inhibitors designed from natural piperidine alkaloids.

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Cláudio Viegas
Vanderlan S Bolzani
Luísa S B Pimentel
Newton G Castro
Rafael F Cabral
Rodrigo S Costa
Corinne Floyd
Mônica S Rocha
Maria C M Young
Eliezer J Barreiro

Keywords

Abstract

Five new piperidine alkaloids were designed from natural (-)-3-O-acetyl-spectaline and (-)-spectaline that were obtained from the flowers of Senna spectabilis (sin. Cassia spectabilis, Leguminosae). Two semi-synthetic analogues (7 and 9) inhibited rat brain acetylcholinesterase, showing IC50 of 7.32 and 15.1 microM, and were 21 and 9.5 times less potent against rat brain butyrylcholinesterase, respectively. Compound 9 (1mg/kg, i.p.) was fully efficacious in reverting scopolamine-induced amnesia in mice. The two active compounds (7 and 9) did not show overt toxic effects at the doses tested in vivo.

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