Publication | Closed Access
Synthesis and Biological Evaluation of 2- and 3-Aminobenzo[<i>b</i>]thiophene Derivatives as Antimitotic Agents and Inhibitors of Tubulin Polymerization
141
Citations
10
References
2007
Year
Pharmaceutical ScienceBioorganic ChemistryColchicine SiteOrganic ChemistryNew SeriesHeterocycle ChemistryPharmaceutical ChemistryMedicinal ChemistryBiological EvaluationAnti-cancer AgentDerivativesBiochemistryDrug DevelopmentTubulin PolymerizationPharmacologyNatural SciencesAntimitotic AgentsMedicineSynthetic ChemistryDrug Discovery
Two new series of inhibitors of tubulin polymerization based on the 2-amino-3-(3,4,5-trimethoxybenzoyl)benzo[b]thiophene molecular skeleton and its 3-amino positional isomer were synthesized and evaluated for antiproliferative activity, inhibition of tubulin polymerization, and cell cycle effects. Although many more 3-amino derivatives have been synthesized so far, the most promising compound in this series was 2-amino-6-methyl-3-(3,4,5-trimethoxybenzoyl)benzo[b]thiophene, which inhibits cancer cell growth at subnanomolar concentrations and interacts strongly with tubulin by binding to the colchicine site.
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