Chinese Journal of Magnetic Resonance ›› 2008, Vol. 25 ›› Issue (4): 514-522.

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Structure Elucidation of Polyene Macrolide Antibiotic Lucensomycin

LI Ning1; LI Wen2; SHA Yi2; HE Jian-yong3; JIANG Qi-hua3; LI Xian1*   

  1. (1.School of Traditional Chinese Materia Medica, Shenyang Parmaceutical University, Shenyang 110016, China; 2.Center of Analysis and Measurement, Shenyang Pharmaceutical University, Shenyang 110016, China; 3.School of Life Science and Bio Pharmaceutics, Shenyang Pharmaceutical University, Shenyang 110016, China)
  • Received:2008-04-11 Revised:2008-05-19 Published:2008-12-05 Online:2009-12-05
  • Contact: Li Xian

Abstract: Polyene macrolide antibiotics are cyclic compounds composed of 25 to 37 carbons, with conjugated polyene fragment and substituted by hydroxyl and glycosidation of aminosaccharide. They have the characteristics of light instability, wide antifungal spectrum, high toxicity by intravenous injection and low toxicity by oral administration. In this study, lucensomycin, an antifungal active substance produced from actinomycetes-1356, was characterized by UV, IR, MS, and NMR spectroscopy. It was found that the 13C NMR chemical shifts of some of the olefinic carbons of this compound were mistakenly assigned in the literature. The regularity for NMR data of polyene macrolide was also summarized in the paper.

Key words: 2D NMR, lucensomycin, assignments, literature correction, regularity summarization

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