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REVISED NMR ASSIGNMENTS FOR THE CHOLECYSTOKININ ANTAGONIST ASPERLICIN
Ist Teil von
The Journal of Antibiotics, 1994/05/25, Vol.47(5), pp.599-601
Ort / Verlag
Tokyo: JAPAN ANTIBIOTICS RESEARCH ASSOCIATION
Erscheinungsjahr
1994
Quelle
Free E-Journal (出版社公開部分のみ)
Beschreibungen/Notizen
Asperlicin (1), a competitive cholecystokinin (CCK) antagonist, produced from Aspergillus alliaceus, was originally characterized primarily by means of X-ray crystallography. The compound contains a 1,4-benzodiazepine ring with a quinazolone fused to the 1,2-positions, and a 3-substituted moiety condensed from tryptophan and leucine. This was the first reported naturally occurring nonpeptide antagonist of a peptide receptor. We have carried out a detailed NMR analysis leading to unambiguous assignments of both super(1)H and super(13)C data for asperlicin, reported herein. The super(1)H NMR spectrum of 1 in CDCl sub(3)-CD sub(3)OD (4:1) showed the presence of 2 methyls, 2 methylenes, 4 methines and 12 well-resolved aromatic protons.