GSK963
目录号: PL11027 纯度: ≥99%
CAS No. :2049868-46-2
商品编号 规格 价格 会员价 是否有货 数量
PL11027-5mg 5mg ¥1607.27 请登录
PL11027-10mg 10mg ¥2596.36 请登录
PL11027-25mg 25mg ¥5192.73 请登录
PL11027-50mg 50mg ¥8345.45 请登录
PL11027-100mg 100mg 询价 询价
PL11027-200mg 200mg 询价 询价
PL11027-10mM*1mLinDMSO 10mM*1mLinDMSO ¥1768.00 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
GSK963
英文名称
GSK963
英文别名
GSK963 Racemate;GSK963
Cas No.
2049868-46-2
分子式
C14H18N2O
分子量
230.31
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
GSK963 是一种手性的、强效的、选择性的受体相互作用蛋白 1 (RIP1) 酶的抑制剂,其 IC50 值为 29 nM。GSK963 对体外小鼠和人细胞的坏死具有强效和选择性的抑制作用。
生物活性
GSK963 is a chiral, highly potent and selective inhibitor of RIP1 kinase, with an IC 50 of 29 nM. GSK963 is a selective and potent inhibitor of necroptosis in murine and human cells in vitro.
性状
Solid
IC50 & Target[1][2]
IC50: 29 nM (RIP1 in FP binding assay).
体外研究(In Vitro)
GSK963 is >10?000-fold selective for RIP1 over 339 other kinases, lacks measurable activity against IDO and has an inactive enantiomer, GSK962, which can be used to confirm on-target effects. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
GSK963 (2 mg/kg) results in a complete protection from TNF+zVAD-induced temperature loss. GSK963 (0.2?mg/kg) also shows a significant response. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
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]. Berger SB, et al. Characterization of GSK963: a structurally distinct, potent and selective inhibitor of RIP1 kinase. Cell Death Discov. 2015 Jul 27;1:15009.
溶解度数据
In Vitro: DMSO : 25 mg/mL (108.55 mM; Need ultrasonic)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