Mechanism of biochemical action of substituted 4-Methylbenzopyran-2-ones. Part 6: hydrolysis of 7,8-diacetoxy-4-methylcoumarin by a novel deacetylase in rat liver microsomes — a simple method for assay and characterisation-Reference-Cited by-同舟云学术

Mechanism of biochemical action of substituted 4-Methylbenzopyran-2-ones. Part 6: hydrolysis of 7,8-diacetoxy-4-methylcoumarin by a novel deacetylase in rat liver microsomes — a simple method for assay and characterisation

Published:2000-01 Issue:1 Volume:8 Page:233-237
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Raj Hanumantha Rao G,Parmar Virinder S,Jain Subhash C,Goel Sanjay,Tyagi Yogesh K,Sharma Sunil K,Olsen Carl E,Wengel Jesper

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference10 articles.

1. Activation of the O-glucuronide of the carcinogen N-hydroxy-N-2-fluorenylacetamide by enzymatic deacetylation in vitro: Formation of fluorenylamine-tRNA adducts

2. Purification and characterization of guinea-pig liver microsomal deacetylase involved in the deacetylation of the O-glucoside of N-hydroxyacetanilide

3. Mechanism of biochemical action of substituted 4-Methylbenzopyran-2-ones. Part 3: A novel mechanism for the inhibition of biological membrane lipid peroxidation by dioxygenated 4-Methylcoumarins mediated by the formation of a stable ADP-Fe-Inhibitor mixed ligand complex

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