Inhibition of Adenosine Deaminase by a Metabolite of the Nephrotoxic Drug, Puromycin Aminonucleoside.
Author:
Publisher
SAGE Publications
Subject
General Biochemistry, Genetics and Molecular Biology
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synthesis, stereochemical characterization, and antimicrobial evaluation of a potentially nonnephrotoxic 3′-C-acethydrazide puromycin analog;Nucleosides, Nucleotides & Nucleic Acids;2017-01-19
2. Synthetic studies toward 3′-C-puromycin analogs;Chemical Data Collections;2016-05
3. Comparative studies of coordination properties of puromycin and puromycin aminonucleoside towards copper(II) ions;Journal of Inorganic Biochemistry;2008-01
4. Synthesis of l,l-puromycin;Tetrahedron;2005-08
5. A role for oxygen free radicals in aminonucleoside nephrosis;Kidney International;1986-02
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