Abstract
Zerumbone was isolated from the rhizomes of Zingiber zerumbet Smith as a potent inhibitor of tumor promoter 12-O-tetradecanoylphorbol-13-acetate-induced Epstein-Barr virus activation. The IC50 value of zerumbone (0.14 microM) is noticeably lower than those of the anti-tumor promoters we have hitherto obtained. Interestingly, alpha-humulene lacking the carbonyl group at the 8-position in zerumbone was inactive (IC50 > 100 microM), while 8-hydroxy-alpha-humulune was markedly active (IC50 = 0.95 microM).
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Anticarcinogenic Agents / chemistry
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Anticarcinogenic Agents / isolation & purification
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Anticarcinogenic Agents / pharmacology*
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Cell Survival / drug effects
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Drug Screening Assays, Antitumor
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Herpesvirus 4, Human / growth & development*
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Humans
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Inhibitory Concentration 50
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Kinetics
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Monocyclic Sesquiterpenes
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Plant Extracts
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Plants, Medicinal
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Sesquiterpenes / chemistry
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Sesquiterpenes / isolation & purification
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Sesquiterpenes / pharmacology*
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Tetradecanoylphorbol Acetate / antagonists & inhibitors*
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Tetradecanoylphorbol Acetate / pharmacology
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Tumor Cells, Cultured
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Virus Activation / drug effects*
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Zingiberales / chemistry*
Substances
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Anticarcinogenic Agents
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Monocyclic Sesquiterpenes
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Plant Extracts
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Sesquiterpenes
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zerumbone
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humulene
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Tetradecanoylphorbol Acetate