The conformations of the macrolide antibiotics erythromycin A, azithromycin and clarithromycin in aqueous solution:: a 1H NMR study

被引:34
作者
Awan, A
Brennan, RJ
Regan, AC
Barber, J [1 ]
机构
[1] Univ Manchester, Sch Pharm & Pharmaceut Sci, Manchester M13 9PL, Lancs, England
[2] Univ Manchester, Dept Chem, Manchester M13 9PL, Lancs, England
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2 | 2000年 / 08期
关键词
D O I
10.1039/b003000g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The conformations of the macrolide antibiotics erythromycin A, clarithromycin and azithromycin in aqueous solution have been determined. All three drugs were found to exist predominantly in a "folded-out" conformation with the sugars in the chair-chair up-up form. In the case of clarithromycin this result is in agreement with the published literature; previous reports suggest that the erythromycin A sugars adopt boat conformations and that azithromycin has a significant folded-in contribution. The discrepancies are discussed in full. Erythromycin A 9-ketone was found to be flexible in the C6-C12 region. We present evidence for a new minor conformation (the 8-endo folded-out conformation) intermediate between the folded-out and folded-in conformations. Evidence for traces of other minor conformations is presented for erythromycin and azithromycin, whereas clarithromycin is conformationally very stable.
引用
收藏
页码:1645 / 1652
页数:8
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