N-benzylpiperidine derivatives of 1,2,4-thiadiazolidinone as new acetylcholinesterase inhibitors

Ana Martinez, Enrique Fernandez, Ana Castro, Santiago Conde, Isabel Rodriguez-Franco, Josep Eladí Baos, Albert Badia

Research output: Contribution to journalArticleResearchpeer-review

84 Citations (Scopus)

Abstract

A new family of 1,2,4-thiadiazolidinone derivatives containing the N-benzylpiperidine fragment has been synthesised. The acetylcholinesterase (AChE) inhibitory activity of all compounds was measured using Ellman's method and some of them turned out to be as potent as tacrine. Furthermore, compound 13 was as active as tacrine in reversing the blockade induced by tubocurarine at rat neuromuscular junction. Additionally, receptor binding studies provided new lead compounds for further development of α2-adrenergic and sigma-receptor antagonists. Molecular dynamic simulation using X-ray crystal, structure of AChE from Torpedo californica was used to explain the possible binding mode of these new compounds. (C) 2000 Editions scientifiques et medicales Elsevier SAS.
Original languageEnglish
Pages (from-to)913-922
JournalEuropean Journal of Medicinal Chemistry
Volume35
DOIs
Publication statusPublished - 1 Jan 2000

Keywords

  • Acetylcholinesterase inhibitors
  • Alzheimer's disease
  • Molecular modelling
  • Thiadiazolidinones
  • α -Adrenoceptor antagonists 2

Fingerprint Dive into the research topics of 'N-benzylpiperidine derivatives of 1,2,4-thiadiazolidinone as new acetylcholinesterase inhibitors'. Together they form a unique fingerprint.

Cite this