CAS NO: | 69408-81-7 |
生物活性 | Amonafide is atopoisomeraseIIinhibitor and DNA intercalator that induces apoptotic signaling by blocking the binding ofTopo IIto DNA. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | Amonafide is a topoisomerase II inhibitor and DNA intercalator that induces apoptotic signaling by blocking the binding of Topo II to DNA[1]. Amonafide produces protein-associated DNA cleavage, single-strand breaks (SSB) and DPC and DNA double-strand cleavage. Amonafide (Nafidimide, 400 nM-2.4 μM) reduces the colony-forming ability of the leukemic cell lines in a dose-dependent manner[2]. Amonafide (0.05-0.4 μg/mL) reduces several tumor growth. However, Amonafide is active against only 12% of tumors compared with standard agents (5-fluorouracil, mitomycin C, cisplatin, and etoposide), which are active against more than 40% of tumors in the human bone marrow inhibitory range[3]. Amonafide inhibits the growth of HT-29, HeLa, and PC-3 cell lines, with IC50s of 4.67, 2.73, and 6.38 μM[4]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 283.33 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C16H17N3O2 | ||||||||||||||||
CAS 号 | 69408-81-7 | ||||||||||||||||
中文名称 | 氨萘非特 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 41.67 mg/mL(147.07 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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