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.
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Awan et al. (2000) studied this question.
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