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Ombrabulin is a synthetic small molecule analogue of combretastatin A4, acting as a vascular disrupting agent (VDA) and antineoplastic. It inhibits tubulin polymerization by binding to the colchicine site of tubulin, leading to destabilization of the cytoskeleton in endothelial cells, causing rapid reduction in tumor blood flow and subsequent tumor necrosis. It was discovered by Ajinomoto and further developed by Sanofi-Aventis for cancer treatment, including solid tumors and soft tissue sarcoma. Development was discontinued after disappointing results in phase III clinical trials.
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