Abstract
A new inhibitor of leukotriene biosynthesis, (+)-10 alpha-hydroxy-4-muurolen-3-one (1), was isolated from fermentations of Favolaschia sp. 87129. Its structure was established by spectroscopic methods. The compound exhibited no antifungal or antibacterial activities. The effects of 1 on leukotriene biosynthesis were compared with (+)-T-cadinol, (-)-3-oxo-T-cadinol, and (+)-3 alpha-hydroxy-T-cadinol, three related sesquiterpenes.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antineoplastic Agents, Phytogenic / chemistry*
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Antineoplastic Agents, Phytogenic / isolation & purification
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Antineoplastic Agents, Phytogenic / toxicity*
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Calcium / pharmacology
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Cell Line
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Cell Survival / drug effects
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Dinoprostone / biosynthesis
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Dinoprostone / blood
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Fermentation
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HL-60 Cells
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HeLa Cells
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Humans
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In Vitro Techniques
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Leukemia L1210
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Leukocytes / drug effects
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Leukocytes / metabolism*
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Leukotriene Antagonists
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Leukotriene C4 / biosynthesis
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Leukotriene C4 / blood
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Leukotrienes / biosynthesis*
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Mice
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Molecular Conformation
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Molecular Structure
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Polyporaceae*
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Rats
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Sesquiterpenes / chemistry*
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Sesquiterpenes / isolation & purification
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Sesquiterpenes / pharmacology
Substances
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10-hydroxy-4-muurolen-3-one
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Antineoplastic Agents, Phytogenic
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Leukotriene Antagonists
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Leukotrienes
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Sesquiterpenes
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Leukotriene C4
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Dinoprostone
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Calcium