Antineoplastic Agents. 548. Synthesis of Iodo- and Diiodocombstatin Phosphate Prodrugs

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• 作者：George R. Pettit ; Heidi J. Rosenberg ; Rachel Dixon ; John C. Knight ; Ernest Hamel ; Jean-Charles Chapuis ; Robin K. Pettit ; Fiona Hogan ; Brandy Sumner ; Kenneth B. Ain ; Brindi Trickey-Platt
• 刊名：Journal of Natural Products
• 出版年：2012
• 出版时间：March 23, 2012
• 年：2012
• 卷：75
• 期：3
• 页码：385-393
• 全文大小：350K
• 年卷期：v.75,no.3(March 23, 2012)
• ISSN：1520-6025

文摘

Toward the objective of designing a structurally modified analogue of the combretastatin A-4 phosphate prodrug (1b) with the potential for increased specificity toward thyroid carcinoma, synthesis of a series of iodocombstatin phosphate (11a鈥?b>h) and diiodocombstatin phosphate prodrugs (12a鈥?b>h) has been accomplished. The diiodo series was obtained via 8a and 9c from condensation of 4 and 6, and the iodo sequence involved a parallel pathway. Both series of iodocombstatins were found to display significant to powerful inhibition of the growth of a panel of human cancer cell lines and of the murine P388 lymphocytic leukemia cell line. Of the diiodo series, 12a was also found to markedly inhibit growth of pediatric neuroblastoma, and monoiodocombstatin 9a strongly inhibited HUVEC growth. Overall, the strongest activity was found against the breast, CNS, leukemia, lung, and prostate cancer cell lines and the least activity against the pancreas and colon lines. Parallel biological investigations of tubulin interaction, antiangiogenesis, and antimicrobial effects were also conducted.