CAS NO: | 1229705-06-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Idasanutlin (RG7388) is a potent and selectiveMDM2antagonist, inhibiting p53-MDM2 binding, with anIC50of 6 nM. | ||||||||||||||||
IC50& Target | IC50: 6 nM (p53-MDM2)[1] | ||||||||||||||||
体外研究 (In Vitro) | Idasanutlin (RG7388) inhibits cell proliferation with IC50of 30 nM, and induces dose-dependent p53 stabilization, cell cycle arrest, as well as cell apoptosis in cancer cells expressing wild-type p53[1]. Idasanutlin (RG7388) (300 nM or 1.8 μM) induces apoptosis in SJSA osteosarcoma cells[2]. | ||||||||||||||||
体内研究 (In Vivo) | Idasanutlin (RG7388, 25 mg/kg p.o.) results in tumor growth inhibition and regression, in the mouse SJSA human osteosarcoma xenograft model[1]. Idasanutlin (RG7388) induces induction of apoptosis and antiproliferation, in the SJSA xenograft model[2]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 616.48 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C31H29Cl2F2N3O4 | ||||||||||||||||
CAS 号 | 1229705-06-9 | ||||||||||||||||
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 : ≥ 45 mg/mL(73.00 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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