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Indole-containing compounds with anti-tubulin and vascular targeting activity

机译:具有抗微管蛋白和血管靶向活性的含吲哚的化合物

摘要

Trimethoxyphenyl substituted indole ligands have been discovered which demonstrate impressive cytotoxicity as well as a remarkable ability to inhibit tubulin assembly. Such compounds as well as related derivatives are excellent clinical candidates for the treatment of cancer in humans. In addition, certain of these ligands, as pro-drugs, may well prove to be tumor selective vascular targeting chemotherapeutic agents or to have vascular targeting activity resulting in the selective prevention and/or destruction of nonmalignant proliferating vasculature.
机译:已经发现三甲氧基苯基取代的吲哚配体表现出令人印象深刻的细胞毒性以及抑制微管蛋白装配的显着能力。此类化合物以及相关衍生物是治疗人类癌症的极佳临床候选药物。另外,这些配体中的某些作为前药可以很好地证明是肿瘤选择性血管靶向化学治疗剂或具有血管靶向活性,从而导致选择性预防和/或破坏非恶性增殖性脉管系统。

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