N alpha-dansyl-L-arginine 4-phenylpiperidine amide. A potent and selective inhibitor of horse serum cholinesterase.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference17 articles.
1. Potent inhibition of thrombin by the newly synthesized arginine derivative No. 805. The importance of stereo-structure of its hydrophobic carboxamide portion
2. Selective inhibition of thrombin by (2R,4R)-4-methyl-1-[N2-[1,2,3,4-tetrahydro-8-quinolinyl)sulfonyl]-L-arginyl]-2-piperidinecarboxylic acid
3. Similarity and dissimilarity in the stereogeometry of the active sites of thrombin, trypsin, plasmin and glandular kallikrein
4. Kinetic Studies on the Selectivity of a Synthetic Thrombin-Inhibitor Using Synthetic Peptide Substrates
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1. Selective Inhibition of Trypsin by (2R,4R)-4-Phenyl-1-[N α-(7- methoxy-2-naphthalenesulfonyl)-l-arginyl]-2-piperidinecarboxylic Acid;Journal of Biological Chemistry;2000-06
2. Amitriptyline: a potent inhibitor of butyrylcholinesterase from human serum;General Pharmacology: The Vascular System;1997-11
3. Territrems: Naturally occurring specific irreversible inhibitors of acetylcholinesterase;Journal of Biomedical Science;1996-01
4. Inhibition kinetics of brain butyrylcholinesterase by Cd2+ and Zn2+, Ca2+ or Mg2+ reactivates the inhibited enzyme;International Journal of Biochemistry;1993-08
5. [19] Synthetic selective inhibitors of thrombin;Methods in Enzymology;1993
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