nystatin-a1 has been researched along with candidin* in 3 studies
3 other study(ies) available for nystatin-a1 and candidin
Article | Year |
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A unified approach to polyene macrolides: synthesis of candidin and nystatin polyols.
Polyene macrolide antibiotics are naturally occurring antifungal agents. Members of this class include amphotericin B, which has been used widely to treat systemic fungal infections. A general synthetic strategy has been devised to prepare polyol chains associated with the polyene macrolides. Cyanohydrin acetonide alkylations were used to assemble the carbon skeleton, and a simple modification of the strategy allowed an advanced intermediate to be converted to either the candidin polyol or the nystatin polyol. The candidin polyol was further elaborated to a protected candidin aglycone. This strategy will be applicable to other members of the polyene macrolide natural products. Topics: Antifungal Agents; Chemistry, Organic; Macrolides; Molecular Structure; Nystatin; Polyenes | 2004 |
Solution NMR structure of five representative glycosylated polyene macrolide antibiotics with a sterol-dependent antifungal activity.
Glycosylated polyene macrolide antibiotics, as nystatins and amphotericins, are amphiphilic structures known to exert antifungal activity by disrupting the fungal cell membrane, leading to leakage of cellular materials, and cell death. This membrane disruption is strongly influenced by the presence and the exact nature of the membrane sterols. The solution structures of five representative glycosylated members, three tetraenes (pimaricin, nystatin A1 and rimocidin) and two heptaenes (candidin and vacidin A) have been calculated using geometric restraints derived from 1H-NMR data and random searches of their conformational space. Despite a different apparent structural order, the NMR solutions structure indicate that the hydroxyl groups all clustered on one side of the rod-shaped structures, and the glycosyl moieties are structurally conserved both in their conformation and their apparent order. The molecular structures afford an understanding of their selective interaction with the membrane sterols and the design of new polyene macrolides with improved activities. Topics: Anti-Bacterial Agents; Antifungal Agents; Candicidin; Glycosylation; Macrolides; Magnetic Resonance Spectroscopy; Natamycin; Nystatin; Polyenes; Sterols | 2002 |
Antifungal activity of candidin, nystatin, eulicin, and stilbamidine against experimental infections in the mouse.
Topics: Animals; Anti-Bacterial Agents; Antifungal Agents; Guanidines; Macrolides; Mice; Mycoses; Nystatin; Stilbamidines; Stilbenes | 1958 |