摘要
1-Aroylindoline, 1-aroyl-1,2,3,4-tetrahydroquinoline, and 1-aroylindole derivatives were synthesized and evaluated for anticancer activity. The 4-amino and 4-hydroxy-1-aroylindoles 26 and 27 with IC50 of 0.9 and 0.6 μM, respectively, exhibited antitubulin activity superior or comparable to that of colchicine and combretastatin A-4. They also showed antiproliferative activity with IC50 of 0.3-5.4 nM in a set of human cancer cell lines.
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 4351-4355 |
| 頁數 | 5 |
| 期刊 | Journal of Medicinal Chemistry |
| 卷 | 51 |
| 發行號 | 14 |
| DOIs | |
| 出版狀態 | 已發佈 - 7月 24 2008 |
UN SDG
此研究成果有助於以下永續發展目標
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SDG 3 良好的健康和福祉
ASJC Scopus subject areas
- 分子醫學
- 藥物發現
指紋
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