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Biochemical Pharmacology
Article
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Biochemical Pharmacology
Article . 1990 . Peer-reviewed
License: Elsevier TDM
Data sources: Crossref
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Aspirin hydrolyzing esterases from rat liver cytosol

Authors: Yuh-Shyong Yang; William B. Jakoby; Dong Hyun Kim;

Aspirin hydrolyzing esterases from rat liver cytosol

Abstract

Unlike most esterases, which are predominantly bound to the microsomal fraction, the enzymes hydrolyzing acetylsalicylic acid are present in an equal amount in the cytosol. Two soluble isozymes were purified to homogeneity from rat liver and characterized as serine esterases with a Mr of 35,000. Both had the wide substrate spectrum characteristic of enzymes active in detoxication. Both had a very low Km for acetylsalicylate. Three other cytoplasmic enzymes active with aspirin were observed but these differed in their high Mr (about 220,000) and their lack of reactivity with antibody to one of the homogeneous isozymes.

Keywords

Aspirin, Hydrolysis, Esterases, Hydrogen-Ion Concentration, Chromatography, DEAE-Cellulose, Paraoxon, Rats, Substrate Specificity, Isoenzymes, Molecular Weight, Nitrophenols, Cytosol, Liver, Chromatography, Gel, Animals

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
views
OpenAIRE UsageCountsViews provided by UsageCounts
downloads
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31
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36
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