RIPA-56
目录号: PL11037 纯度: ≥99%
CAS No. :1956370-21-0
商品编号 规格 价格 会员价 是否有货 数量
PL11037-10mg 10mg ¥884.00 请登录
PL11037-50mg 50mg ¥2652.00 请登录
PL11037-100mg 100mg ¥4259.00 请登录
PL11037-200mg 200mg ¥7473.00 请登录
PL11037-500mg 500mg 询价 询价
PL11037-1g 1g 询价 询价
PL11037-10mM*1mLinDMSO 10mM*1mLinDMSO ¥972.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
RIPA-56
英文名称
RIPA-56
英文别名
RIPA-56;RIPA56;N-Benzyl-N-hydroxy-2,2-dimethylbutanamide
Cas No.
1956370-21-0
分子式
C13H19NO2
分子量
221.30
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
RIPA-56 是一种高效选择和代谢稳定的受体相互作用蛋白 1 (RIP1) 抑制剂,IC50 为 13 nM。RIPA-56 可用于研究全身炎症反应综合征。
生物活性
RIPA-56 is a highly potent, selective, and metabolically stable inhibitor of receptor-interacting protein 1 (RIP1) with an IC 50 of 13 nM. RIPA-56 can be used for the treatment of systemic inflammatory response syndrome.
性状
Solid
IC50 & Target[1][2]
IC50: 13 nM (RIP1)
体外研究(In Vitro)
RIPA-56 shows efficient inhibition of RIP1 kinase activity, with an IC50 of 13 nM and no inhibition of RIP3 kinase activity at a 10 μM concentration. RIPA-56 also demonstrates potency in protection of murine L929 cells from TNFα/z-VAD-FMK (TZ)-induced necrosis (EC50=27 nM). has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
In the SIRS mice disease model, RIPA-56 efficiently reduces tumor necrosis factor alpha (TNFα)-induced mortality and multi-organ damage. Compared to known RIP1 inhibitors, RIPA-56 is potent in both human and murine cells, is much more stable in vivo, and is efficacious in animal model studies. RIPA-56 has an impressive PK profile in mice with a 3.1 h half-life, 22% oral bioavailability (P.O.), and 100% bioavailability from intraperitoneal injection (I.P.). has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Ren Y, et al. Discovery of a Highly Potent, Selective, and Metabolically Stable Inhibitor of Receptor-InteractingProtein 1 (RIP1) for the Treatment of Systemic Inflammatory Response Syndrome. J Med Chem. 2017 Feb 9;60(3):972-986.
溶解度数据
In Vitro: DMSO : ≥ 100 mg/mL (451.88 mM)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2