Structural elucidation of rokitamycin, midecamycin and erythromycin metabolites formed by pathogenicNocardia
Author:
Publisher
Wiley
Subject
General Materials Science,General Chemistry
Reference22 articles.
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2. Inactivation of Kanamycin A by Phosphorylation in PathogenicNocardia
3. Inactivation of rifampin by Nocardia brasiliensis
4. Inactivated products of rifampicin by pathogenic Nocardia spp.: Structures of glycosylated and phosphorylated metaholites of rifampicin and 3-formylrifamycin SV.
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1. Controlling the Site Selectivity in Acylations of Amphiphilic Diols: Directing the Reaction toward the Apolar Domain in a Model Diol and the Midecamycin A1 Macrolide Antibiotic;The Journal of Organic Chemistry;2022-07-08
2. Recent Progress of Taxonomic Studies on Pathogenic Nocardia and Usefulness of the Bacteria for the Studies on Secondary Metabolites and Antibiotic Resistant Mechanisms;Nippon Ishinkin Gakkai Zasshi;2010
3. Isolation and Structural Characterization of Siderophores, Madurastatins, Produced by a Pathogenic Actinomadura madurae;The Journal of Antibiotics;2004
4. Structures of ADP-Ribosylated Rifampicin and Its Metabolite: Intermediates of Rifampicin-ribosylation by Mycobacterium smegmatis DSM43756.;The Journal of Antibiotics;2000
5. Inactivation of Fusidic Acid by Pathogenic Nocardia.;The Journal of Antibiotics;1999
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