Abstract
In the course of our continuing search for new antitumor-antibiotics from marine-derived actinomycete bacteria, four new cytotoxic compounds, designated as daryamides A (1), B (2), and C (3) and (2E,4E)-7-methylocta-2,4-dienoic acid amide (4), were isolated from the culture broth of a marine-derived Streptomyces strain CNQ-085. The structures of these new compounds were assigned by detailed interpretation of spectroscopic data. The relative configuration of 1 was determined by comprehensive NMR analysis, while the absolute configuration of 1 was determined as 4S,5R using the modified Mosher method. The daryamides show weak to moderate cytotoxic activity against the human colon carcinoma cell line HCT-116 and very weak antifungal activities against Candida albicans.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Antibiotics, Antineoplastic / chemistry
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Antibiotics, Antineoplastic / isolation & purification*
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Antibiotics, Antineoplastic / pharmacology
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California
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Candida albicans / drug effects
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Drug Screening Assays, Antitumor
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Humans
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Methicillin Resistance / drug effects
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Microbial Sensitivity Tests
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Molecular Structure
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Nuclear Magnetic Resonance, Biomolecular
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Polyenes / chemistry
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Polyenes / isolation & purification*
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Polyenes / pharmacology
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Polyunsaturated Alkamides / chemistry
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Polyunsaturated Alkamides / isolation & purification*
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Polyunsaturated Alkamides / pharmacology
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Staphylococcus aureus / drug effects
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Streptomyces / chemistry*
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Tumor Cells, Cultured
Substances
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Antibiotics, Antineoplastic
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Polyenes
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Polyunsaturated Alkamides
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daryamide A
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daryamide B
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daryamide C