CAS NO: | 309271-94-1 |
生物活性 | Inauhzin is a dualSirT1/IMPDH2inhibitor, and acts as an activatorp53, used in the research ofcancer. | ||||||||||||||||
IC50& Target[3] |
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体外研究 (In Vitro) | Inauhzin (10 μM) induces p53 levels as effectively as actinomycin D (10 nM), and mediates p53-dependent cytotoxicity through its specific functional groups in human lung carcinoma H460 cells. Inauhzin (2 μM) induces p53 level and activity as well as p53-dependent apoptosis. Inauhzin also stabilizes p53 and inhibits its ubiquitylation. Inauhzin induces acetylation of p53 in H460 cells, but not tubulin, which is affected by knockdown of SIRT1[1]. Inauhzin (0-2 μM) significantly enhances the expression level and activity of p53 in HCT116p53+/+cells and enhances the expression level and activity of p53 in H460 cells in a dose-dependent manner. Inauhzin and Nutlin-3 demonstrate synergistic cytotoxicity in the Nutlin-3 low-sensitive cells. Inauhzin and Nutlin-3 synergistically induce p53-dependent apoptosis[2]. Inauhzin targets both SirT1 and IMP dehydrogenase 2 (IMPDH2), and acts as a potent p53 activator[3]. | ||||||||||||||||
体内研究 (In Vivo) | Inauhzin (30 mg/kg, i.p.) effectively induces apoptosis and suppresses tumour growth of H460 xenograft harbouring p53[1]. Inauhzin (30 mg/kg, i.p.) reduces the HCT116 tumor volume by appr 70%. Inauhzin (15 mg/kg) in combination with 150 mg/kg of Nutlin-3 demonstrates a significant synergy on p53 induction, apoptosis and tumor suppression of HCT116p53+/+xenografts[2]. | ||||||||||||||||
分子量 | 469.58 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C25H19N5OS2 | ||||||||||||||||
CAS 号 | 309271-94-1 | ||||||||||||||||
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 : 100 mg/mL(212.96 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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