Abstract
During the course of a structure-activity relationship (SAR) study on novel depsinonapeptide pseudomycin B, we synthesized a total of 12 8-amidopseudomycin analogues via standard two-step sequence from either ZPSB 2 or AllocPSB 3. A number of these amides exhibited good in vitro antifungal activities.
MeSH terms
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Animals
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Antifungal Agents / chemical synthesis*
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Antifungal Agents / chemistry
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Antifungal Agents / pharmacology
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Aspergillus fumigatus / drug effects
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Candida albicans / drug effects
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Candidiasis / drug therapy
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Combinatorial Chemistry Techniques
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Cryptococcus neoformans / drug effects
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Dose-Response Relationship, Drug
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Mice
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Microbial Sensitivity Tests
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Models, Animal
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Nuclear Magnetic Resonance, Biomolecular
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Peptides, Cyclic / chemical synthesis
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Peptides, Cyclic / chemistry
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Peptides, Cyclic / pharmacology*
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Structure-Activity Relationship
Substances
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Antifungal Agents
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Peptides, Cyclic
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pseudomycin B