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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/33748
Title: 
New selective acetylcholinesterase inhibitors designed from natural piperidine alkaloids
Author(s): 
Institution: 
  • Universidade Federal do Rio de Janeiro (UFRJ)
  • Universidade Estadual Paulista (UNESP)
  • Inst Bot
ISSN: 
0968-0896
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 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.
Issue Date: 
1-Jul-2005
Citation: 
Bioorganic & Medicinal Chemistry. Oxford: Pergamon-Elsevier B.V., v. 13, n. 13, p. 4184-4190, 2005.
Time Duration: 
4184-4190
Publisher: 
Elsevier B.V.
Keywords: 
  • piperidine alkaloids
  • acetylcholinesterase inhibitors
  • Alzheimer's disease
  • Senna spectabilis
Source: 
http://dx.doi.org/10.1016/j.bmc.2005.04.030
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/33748
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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