| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2487697 | Journal of Pharmaceutical Sciences | 2007 | 7 Pages |
Abstract
Four solvates of erythromycin have been crystallographically characterized. The solvates of THF and dioxane are very similar but differ in notable ways. The isopropanol solvate exhibits uncommon modes of hydrogen bonding, which have previously been seen only in the erythomycin B hydrate. The methanol solvate is strikingly similar to the methanol solvate of 6-O-methyl erythromycin.
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Drug Discovery
Authors
Rodger Henry, Geoff G.Z. Zhang,