New selective acetylcholinesterase inhibitors designed from natural piperidine alkaloids


Autoria(s): Viegas, C.; Bolzani, Vanderlan da Silva; Pimentel, LSB; Castro, N. G.; Cabral, R. F.; Costa, R. S.; Floyd, C.; Rocha, M. S.; Young, MCM; Barreiro, E. J.; Fraga, CAM
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/07/2005

Resumo

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 mu M, and were 21 and 9.5 times less potent against rat brain butyrylcholinesterase, respectively. Compound 9 (1 mg/kg, ip) 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. (c) 2005 Elsevier Ltd. All rights reserved.

Formato

4184-4190

Identificador

http://dx.doi.org/10.1016/j.bmc.2005.04.030

Bioorganic & Medicinal Chemistry. Oxford: Pergamon-Elsevier B.V., v. 13, n. 13, p. 4184-4190, 2005.

0968-0896

http://hdl.handle.net/11449/33748

10.1016/j.bmc.2005.04.030

WOS:000229811900006

Idioma(s)

eng

Publicador

Elsevier B.V.

Relação

Bioorganic & Medicinal Chemistry

Direitos

closedAccess

Palavras-Chave #piperidine alkaloids #acetylcholinesterase inhibitors #Alzheimer's disease #Senna spectabilis
Tipo

info:eu-repo/semantics/article