A number of indole-3-glyoxylamides have previously been reported as tubulin polymerization inhibitors, although none has yet been successfully developed clinically. We report here a new series of related compounds, modified according to a strategy of reducing aromatic ring count and introducing a greater degree of saturation, which retain potent tubulin polymerization activity but with a distinct SAR from previously documented libraries. A subset of active compounds from the reported series is shown to interact with tubulin at the colchicine binding site, disrupt the cellular microtubule network, and exert a cytotoxic effect against multiple cancer cell lines. Two compounds demonstrated significant tumor growth inhibition in a mouse xenograft model of head and neck cancer, a type of the disease which often proves resistant to chemotherapy, supporting further development of the current series as potential new therapeutics.
An Orally Bioavailable, Indole-3-glyoxylamide Based Series of Tubulin Polymerization Inhibitors Showing Tumor Growth Inhibition in a Mouse Xenograft Model of Head and Neck Cancer.
H. Colley,M. Muthana,S. Danson,Lucinda V. Jackson,M. Brett,Joanne Harrison,Sean F Coole,D. P. Mason,Luke R Jennings,Melanie H. Wong,V. Tulasi,D. Norman,P. Lockey,L. Williams,A. Dossetter,E. Griffen,M. Thompson
Published 2015 in Journal of Medicinal Chemistry
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- Publication year
2015
- Venue
Journal of Medicinal Chemistry
- Publication date
2015-12-01
- Fields of study
Medicine, Chemistry
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- Source metadata
Semantic Scholar, PubMed
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