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3. Slow detection reaction can mimic initial inhibition of an enzymic reaction. Stojan J. J Enzyme Inhib; 2001; 16(2):89-94. PubMed ID: 11342277 [Abstract] [Full Text] [Related]
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5. Ambenonium is a rapidly reversible noncovalent inhibitor of acetylcholinesterase, with one of the highest known affinities. Hodge AS, Humphrey DR, Rosenberry TL. Mol Pharmacol; 1992 May 05; 41(5):937-42. PubMed ID: 1588924 [Abstract] [Full Text] [Related]
6. Catalysis by acetylcholinesterase: evidence that the rate-limiting step for acylation with certain substrates precedes general acid-base catalysis. Rosenberry TL. Proc Natl Acad Sci U S A; 1975 Oct 05; 72(10):3834-8. PubMed ID: 668 [Abstract] [Full Text] [Related]
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9. Acetylcholinesterase: theory of noncompetitive inhibition. Froede HC, Wilson IB, Kaufman H. Arch Biochem Biophys; 1986 Jun 05; 247(2):420-3. PubMed ID: 3717952 [Abstract] [Full Text] [Related]
10. Direct determination of acetyl-enzyme intermediate in the acetylcholinesterase-catalyzed hydrolysis of acetylcholine and acetylthiocholine. Froede HC, Wilson IB. J Biol Chem; 1984 Sep 10; 259(17):11010-3. PubMed ID: 6469995 [Abstract] [Full Text] [Related]
15. Butyrylcholinesterase: inhibition by arsenite, fluoride, and other ligands, cooperativity in binding. Page JD, Wilson IB, Silman I. Mol Pharmacol; 1985 Apr 10; 27(4):437-43. PubMed ID: 3982389 [Abstract] [Full Text] [Related]
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