MSC2360844 hemifumarate

(Synonyms: MSC2360844 hemifumarate; IOA-244 hemifumarate)
目录号: PL09771 纯度: ≥99%
MSC2360844 hemifumarate 是一种有效的,具有口服活性的选择性 PI3Kδ 抑制剂,IC50为 145 nM。MSC2360844 hemifumarate 对一组 278 种其他激酶显示出高度选择性。
CAS No. :1621688-31-0
商品编号 规格 价格 会员价 是否有货 数量
PL09771-5mg 5mg ¥4821.00 请登录
PL09771-10mg 10mg ¥8036.00 请登录
PL09771-25mg 25mg ¥15269.00 请登录
PL09771-50mg 50mg ¥24912.00 请登录
PL09771-100mg 100mg ¥37770.00 请登录
PL09771-200mg 200mg 询价 询价
PL09771-500mg 500mg 询价 询价
PL09771-10mM*1mLinDMSO 10mM*1mLinDMSO ¥6204.00 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。
*注意事项:下单时请联系销售核实产品价格及货期,避免后续产生不便,感谢支持!
中文名称
MSC2360844 hemifumarate
英文名称
MSC2360844 hemifumarate
英文别名
MSC2360844 hemifumarate;Roginolisib hemifumarate
Cas No.
1621688-31-0
分子式
C11H18FN2O14P3
分子量
514.19
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
详情描述
MSC2360844 hemifumarate 是一种有效的,具有口服活性的选择性 PI3Kδ 抑制剂,IC50为 145 nM。MSC2360844 hemifumarate 对一组 278 种其他激酶显示出高度选择性。
产品详情
MSC2360844 hemifumarate 是一种有效的,具有口服活性的选择性 PI3Kδ 抑制剂,IC50为 145 nM。MSC2360844 hemifumarate 对一组 278 种其他激酶显示出高度选择性。
生物活性
MSC2360844 hemifumarate is a potent, orally active and selective PI3Kδ inhibitor, with an IC 50 of 145 nM. MSC2360844 hemifumarate shows highly selective against a panel of 278 additional kinases.
性状
Solid
IC50 & Target[1][2]
PI3Kδ 145 nM (IC50)
体外研究(In Vitro)
MSC2360844 hemifumarate (0-10 μM; 1 hours) completely abolished BCR-induced pAkt in Ramos B cells in a concentration-dependent manner with IC50 values of 280?nM.
MSC2360844 hemifumarate inhibits B cell proliferation in a concentration-dependent manner with an IC50 of 48?nM. MSC2360844 hemifumarate blocks BCR- and TCR-mediated responses in lymphocytes and TLR-induced IFNα by pDC in human primary cells. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
MSC2360844 hemifumarate (6.6-66 mg/kg; daily from week 2 to 10) ameliorates disease manifestations in a murine SLE model. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: NZB/W F1 fema
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Haselmayer P, et al. Characterization of Novel PI3Kδ Inhibitors as Potential Therapeutics for SLE and Lupus Nephritis in Pre-Clinical Studies. Front Immunol. 2014 May 22;5:233.
溶解度数据
In Vitro: DMSO : 100 mg/mL (171.05 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