The Journal of Antibiotics
Online ISSN : 1881-1469
Print ISSN : 0021-8820
ISSN-L : 0021-8820
CHLOROPOLYSPORINS A, B AND C, NOVEL GLYCOPEPTIDE ANTIBIOTICS FROM FAENIA INTERJECTA SP. NOV.
III. STRUCTURE ELUCIDATION OF CHLOROPOLYSPORINS
TOSHIO TAKATSUSHUJI TAKAHASHIMUTSUO NAKAJIMATATSUO HANEISHITAKEMICHI NAKAMURAHARUMITSU KUWANOTAKESHI KINOSHITA
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1987 Volume 40 Issue 7 Pages 933-940

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Abstract
Structure elucidations of chloropolysporins A, B and C were achieved mainly by chemical degradation studies. These components possessed the same pseudoaglycone in common and their structures were closely related to that of β-avoparcin. The structures of chloropolysporins differ from that of β-avoparcin in the presence of vancomycmic acid moiety instead of monodechlorovancomycinic acid moiety and glucose, not ristosaminylglucose, in its side chain. Chloropolysporin C was identified as derhamnosylchloropolysporin B based on its 1H NMR and mass spectral analysis and degradation studies. Two minor components, chloropolysporins D and E, were identified as the epimers of each of chloropolysporins B and C, respectively, based on their Cotton effects and retention times on reverse phase HPLC.
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© Japan Antibiotics Research Association
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