Structural Investigation of the Antibiotic Ristomycin A 13C-Nmr Spectral Analysis of the Interglycosidic Linkages of the Heterotetrasaccharide Side-Chain

A. Neszmélyi, A. Lipták, F. Sztaricskai, R. Bognár

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

By 13C-NMR studies on Ia, IIa, IIb and IVa obtained by the chemical degradation of ristomycin A and on several synthetic model compounds it has been proved that an O-ß-Darabinopyranosyl -(1→2)-O-α-D-mannopyranosyl-(1→2)-O-[α-L-rhamnopyranosyl-(l→6)]-Dglucopyranosyl heterotetrasaccharide moiety is connected to the aglycone of the antibiotic.

Original languageEnglish
Pages (from-to)974-975
Number of pages2
JournalThe Journal of Antibiotics
Volume31
Issue number10
DOIs
Publication statusPublished - 1978

ASJC Scopus subject areas

  • Pharmacology
  • Drug Discovery

Fingerprint Dive into the research topics of 'Structural Investigation of the Antibiotic Ristomycin A <sup>13</sup>C-Nmr Spectral Analysis of the Interglycosidic Linkages of the Heterotetrasaccharide Side-Chain'. Together they form a unique fingerprint.

  • Cite this