Literature DB >> 5810051

The inhibition of acetylcholinesterase by oxime carbamates.

P Jewess, N R McFarlane, R B Beechey.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1969        PMID: 5810051      PMCID: PMC1184830          DOI: 10.1042/bj1140014pb

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


× No keyword cloud information.
  5 in total

1.  ACETYLCHOLINESTERASE: TRIMETHYLAMMONIUM-ION INHIBITION OF DEACETYLATION.

Authors:  R M KRUPKA
Journal:  Biochemistry       Date:  1964-11       Impact factor: 3.162

2.  Turnover number of acetyl-cholinesterase.

Authors:  I B WILSON; M A HARRISON
Journal:  J Biol Chem       Date:  1961-08       Impact factor: 5.157

3.  Carbamyl derivatives of acetylcholinesterase.

Authors:  I B WILSON; M A HARRISON; S GINSBURG
Journal:  J Biol Chem       Date:  1961-05       Impact factor: 5.157

4.  Acetylcholinesterase. X. Mechanism of the catalysis of acylation reactions.

Authors:  I B WILSON; F BERGMANN; D NACHMANSOHN
Journal:  J Biol Chem       Date:  1950-10       Impact factor: 5.157

5.  Hydrolysis of neutral substrates by acetylcholinesterase.

Authors:  R M Krupka
Journal:  Biochemistry       Date:  1966-06       Impact factor: 3.162

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.