Stereoselective inhibition of butyrylcholinesterase by enantiomers ofexo- andendo-2-norbornyl-N-n-butylcarbamates
Author:
Affiliation:
1. Division of Neurosurgery, Chung Shan Medical University Hospital, Taichung, Taiwan
2. Department of Chemistry, National Chung-Hsing University, Taichung, Taiwan
Publisher
Informa UK Limited
Subject
Drug Discovery,Pharmacology,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.3109/14756360902888200
Reference53 articles.
1. Molecular and cellular biology of cholinesterases
2. Enhancing cocaine metabolism with butyrylcholinesterase as a treatment strategy
3. Crystal Structure of Human Butyrylcholinesterase and of Its Complexes with Substrate and Products
4. Photoreversible Inhibition of Cholinesterases: Catalytic Serine-Labeled Caged Butyrylcholinesterase
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1. S-endo-2-Norbornyl-N-n-butylcarbamate as a PotentialPseudomonasLipase Inhibitor to Probe the Enantioselectivity of the Enzyme by Kinetic and Molecular Docking Evaluation;Journal of the Chinese Chemical Society;2016-06-30
2. Kinetics and Protein-Inhibitor Docking Studies of Enantiomers of exo-2-Norbornyl-N-n-butylcarbamates as Pseudomonas Lipase Inhibitors to Probe the Enantioselectivity of the Enzyme;Journal of the Chinese Chemical Society;2012-01
3. Synthesis and Pseudomonas Lipase Inhibition Study of Stereoisomers of Decahydro-2-naphthyl-N-n-butylcarbamate;Protein & Peptide Letters;2011-11-01
4. Stereo-specific inhibition of acetyl- and butyryl-cholinesterases by enantiomers of cis,cis-decahydro-2-naphthyl-N-n-butylcarbamate;Journal of Biochemical and Molecular Toxicology;2011-05-31
5. Stereoselective Inhibition of Cholesterol Esterase by Enantiomers of exo- and endo-2-Norbornyl-N–n-butylcarbamates;The Protein Journal;2011-03
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