CAS NO: | 293762-45-5 |
包装 | 价格(元) |
5mg | 询价 |
10mg | 询价 |
25mg | 询价 |
50mg | 询价 |
100mg | 询价 |
生物活性 | Ro 90-7501 is anamyloid β42(Aβ42) fibril assemblyinhibitor that reducesAβ42-induced cytotoxicity (EC50of 2 μM). Ro 90-7501 inhibitsATMphosphorylation and DNA repair. RO 90-7501 selectively enhancestoll-like receptor 3(TLR3) andRIG-I-like receptor(RLR) ligand-induced IFN-β gene expression and antiviral response[2]. Ro 90-7501 also inhibitsproteinphosphatase5 (PP5)in a TPR-dependent manner[3]. Ro 90-7501 has significant radiosensitizing effects on cervicalcancercells[4]. | ||||||||||||||||
IC50& Target[1][3] |
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体外研究 (In Vitro) | Ro 90-7501 significantly enhances radiosensitivity compared with control HeLa and ME-180 cells. Ro 90-7501 significantly increases apoptosis and impaired cell cycle after irradiation. Ro 90-7501 suppresses the phosphorylation of ATM and its downstream proteins, such as H2AX, Chk1, and Chk2, after irradiation[1]. | ||||||||||||||||
体内研究 (In Vivo) | Ro 90-7501 (5 μg/g; intraperitoneal injection; daily; for 21 days; female BALB/c nude mice) treatment significantly delays tumor growth and significantly decreases tumor volume[1].
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分子量 | 340.38 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H16N6 | ||||||||||||||||
CAS 号 | 293762-45-5 | ||||||||||||||||
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(122.42 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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