The Synthesis and Tubulin Binding Activity of Thiophene-Based Analogues of Combretastatin A-4
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Flynn, Bernard
Flynn, Guy
Hamel, Ernest
Jung, M Katherine
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Pergamon-Elsevier Ltd
Abstract
A number of analogues of combretastatin A-4 (1), containing a thiophene ring interposed between the two phenyl groups, have been prepared. The synthesis of these compounds employed a combination of palladium-mediated coupling and iodocyclization techniques. The thiophene compounds 11, 14, 18, and 19 also represent non-benzofused analogues of some recently described tubulin binding benzo[b]thiophenes 3-5. The most active thiophene compounds identified in this study were 11, 14, and 18. Overall they are less active than 1 but exhibit comparable activity to the most active of the benzo[b]thiophenes 3-5. A structure-activity relationship of these compounds is considered.
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Bioorganic and Medicinal Chemistry Letters
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2037-12-31
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