Abstract
Kottamides A-D (1-4), novel 2,2,5-trisubstituted imidazolone-containing alkaloids, were isolated from the New Zealand endemic ascidian Pycnoclavella kottae and structurally characterized using 15N natural abundance 2-D NMR in addition to standard spectroscopic methods. The kottamides exhibited anti-inflammatory and anti-metabolic activity as well as cytotoxicity toward tumor cell lines.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Alkaloids / chemistry
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Alkaloids / isolation & purification*
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Alkaloids / pharmacology
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Amino Acid Sequence
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Animals
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Anti-Bacterial Agents
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Anti-Infective Agents / chemistry
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Anti-Infective Agents / isolation & purification*
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Anti-Infective Agents / pharmacology
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Antifungal Agents / chemistry
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Antifungal Agents / isolation & purification*
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Antifungal Agents / pharmacology
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Antineoplastic Agents / chemistry
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Antineoplastic Agents / isolation & purification*
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Antineoplastic Agents / pharmacology
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Antiviral Agents / chemistry
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Antiviral Agents / isolation & purification*
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Antiviral Agents / pharmacology
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Bacillus subtilis / drug effects
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Candida albicans / drug effects
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Drug Screening Assays, Antitumor
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Escherichia coli / drug effects
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Indazoles / chemistry
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Indazoles / isolation & purification*
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Indazoles / pharmacology
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Inhibitory Concentration 50
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Leukemia
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Leukemia P388
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Mice
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Molecular Structure
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New Zealand
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Nuclear Magnetic Resonance, Biomolecular
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Stereoisomerism
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Trichophyton / drug effects
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Tumor Cells, Cultured / drug effects
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Urochordata / chemistry*
Substances
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Alkaloids
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Anti-Bacterial Agents
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Anti-Infective Agents
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Antifungal Agents
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Antineoplastic Agents
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Antiviral Agents
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Indazoles