| Literature DB >> 10348043 |
N Matsumoto1, T Tsuchida, H Nakamura, R Sawa, Y Takahashi, H Naganawa, H Iinuma, T Sawa, T Takeuchi, M Shiro.
Abstract
The absolute structure of a new antibiotic lactonamycin is described. The NMR studies deduced one of four possible structures for the aglycon attached by a rhodinose through glycosidic bond. The stereochemistry of the sugar obtained by an acid hydrolysis was determined to be L-form by measuring optical rotation. The stereochemistry of the aglycon was determined by X-ray crystallographic analysis.Entities:
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Year: 1999 PMID： 10348043 DOI： 10.7164/antibiotics.52.276
Source DB: PubMed Journal: J Antibiot (Tokyo) ISSN： 0021-8820 Impact factor: 2.649