耗材描述
β-Lapachone
产品活性:β-Lapachone (ARQ-501;NSC-26326) 是一种天然的萘醌类化合物,是拓扑异构酶 I (topoisomerase I) 抑制剂,通过抑制细胞周期进程来诱导细胞凋亡。
产品来源: https://www.medchemexpress.cn/_beta_-Lapachone.html
研究领域:Cell Cycle/DNA Damage | Autophagy | Apoptosis
作用靶点:Topoisomerase | Autophagy | Apoptosis
来源:植物 | 其他科
结构分类:醌类 | 萘醌类 | 结构分类
In Vitro: β-Lapachone is a topoisomerase I inhibitor. β-Lapachone (25 μM) inhibits camptothecin-induced DNA cleavage. β-Lapachone (10-40 μM) significantly reduces the colony-forming ability of CHO cells, and is cytotoxic in S phase. β-Lapachone at above 10 μM, causes a heavy DNA-strand breaks in CHO cells. β-Lapachone (10 μM) suppresses JCPyV replication in IMR-32 cells. β-Lapachone (1.0?μM) potently affects JCPyV propagation in JCI cells. β-Lapachone (0.01-0.1 μM) inhibits VP1 production in JCI cells.
In Vivo: β-Lapachone (0.066%) ameliorates cisplatin-induced renal injury and when in combination with cisplatin, the affect is more significant in mice. β-Lapachone increases Mre11-Rad50-Nbs1 (MRN) complex expression in mice.
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