Study of a potential inhibitor of acetylcholinesterase using UV spectrophotometry, NMR spectroscopy and molecular modeling-Reference-Cited by-同舟云学术

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Study of a potential inhibitor of acetylcholinesterase using UV spectrophotometry, NMR spectroscopy and molecular modeling

Published:2006 Issue:2 Volume:19 Page:148-156
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Correia Isabelle,Ronzani Nello,Platzer Nicole,Doan Bich-Thuy,Beloeil Jean-Claude

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference26 articles.

1. Atomic Structure of Acetylcholinesterase from Torpedo californica : A Prototypic Acetylcholine-Binding Protein

2. Studies on a new series of THA analogues: Effects of the aromatic residues that line the gorge of AChE

3. Anticholinesterase activity of a new carbamate, heptylphysostigmine, in view of its use in patients with Alzheimer-type dementia

4. Quaternary ligand binding to aromatic residues in the active-site gorge of acetylcholinesterase.

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1. Acid-promoted synthesis and photophysical properties of substituted acridine derivatives;Organic & Biomolecular Chemistry;2020

2. Applications for Treatment of Neurodegenerative Diseases;Progress in Drug Research;2017

3. Heterocyclic Scaffolds for the Treatment of Alzheimer's Disease;Current Pharmaceutical Design;2016-08-01

4. Recent Advances in the Chemistry of Acridines;Advances in Heterocyclic Chemistry;2015

5. New potential AChE inhibitor candidates;European Journal of Medicinal Chemistry;2009-09

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