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  • 1
    Electronic Resource
    Electronic Resource
    Purification of macrolide 2′-phosphotransferase fromStreptomyces coelicolor Müller (1990)
    Springer
    Journal of industrial microbiology and biotechnology 6 (1990), S. 295-297 
    Details
    ISSN: 1476-5535
    Keywords: Phosphorylation ; Oleandomycin ; Macrolide 2′-phosphotransferase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary An enzyme that catalyzes 2′-O-phosphorylation of oleandomycin and several other macrolide antibiotics has been purified approximately 47-fold from cell-free extracts ofStreptomyces coelicolor Müller, NRRL 3532 (UC™ 5240). The reaction product was verified as being oleandomycin-2′-O-phosphate by mass spectrometry. As a result of purification, the enzyme was separated from two lincosaminide inactivating enzyme activities also present in the cell-free extract.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01575877
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  • 2
    Electronic Resource
    Electronic Resource
    The Pharmacokinetics of Trilostane and Ketotrilostane in an Interconverting System in the Rat (1992)
    Springer
    Pharmaceutical research 9 (1992), S. 464-468 
    Details
    ISSN: 1573-904X
    Keywords: trilostane ; ketotrilostane ; reversible metabolism ; pharmacokinetics ; metabolic interconversion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics of trilostane and one of its metabolites ketotrilostane are described and characterized in the rat following the separate intravenous administration of trilostane and ketotrilostane. It was noted during these studies that the parent compound and its metabolite undergo metabolic interconversion–trilostane producing ketotrilostane and ketotrilostane generating trilostane. This result means that trilostane is conserved in the body by interconversion-being metabolized to ketotrilostane and then subsequently back to the “parent” drug, trilostane.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1015828027060
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    Paper (German National Licenses)
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