RO2959 monohydrochloride
目录号: PL02151 纯度: ≥99%
CAS No. :2309172-44-7
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中文名称
RO2959 monohydrochloride
英文名称
RO2959 monohydrochloride
英文别名
RO2959 monohydrochloride;RO2959 Hydrochloride;RO2959 (monohydrochloride);2,6-difluoro-N-[5-[4-methyl-1-(5-methyl-1,3-thiazol-2-yl)-3,6-dihydro-2H-pyridin-5-yl]pyrazin-2-yl]benzamide;hydrochloride;RO2959 HCl;C21H20ClF2N5OS;AOB3633;SYN5226;2,6-Difluoro-N-(5-(4-methyl-1-(5-methylthiazol-2-yl)-1,2,5,6-tetrahydropyridin-3-yl)pyrazin-2-yl)benzamide hydrochloride(1:x);2,6-Difluoro-N-{5-[4-m
Cas No.
2309172-44-7
分子式
C21H20ClF2N5Os
分子量
463.93
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)
产品详情
RO2959 monohydrochloride 是一种有效的选择性 CRAC 通道抑制剂,IC50 为 402 nM。RO2959 monohydrochloride 是由 Orai1/Stim1 通道介导的钙存储进入 (SOCE) 的有效阻滞剂,IC50 为 25 nM。RO2959 monohydrochloride 还是人 IL-2 产生的有效抑制剂,有效阻断 T 细胞受体触发的基因表达和 T 细胞功能途径。
生物活性
RO2959 monohydrochloride is a potent and selective CRAC channel inhibitor with an IC 50 of 402 nM. RO2959 monohydrochloride is a potent blocker of store operated calcium entry (SOCE) mediated by Orai1/Stim1 channels with an IC 50 of 25 nM. RO2959 monohydrochloride is also a potent inhibitor of human IL-2 production, and potently blocks T cell receptor triggered gene expression and T cell functional pathways.
性状
Solid
IC50 & Target[1][2]
CRAC channel 402 nM (IC50) Orai1/Stim1 channels
体外研究(In Vitro)
RO2959 inhibits Orai1 and Orai3 with IC50 values of 25 nM and 530 nM, respectively. RO2959 blocks store operated calcium entry (SOCE) in activated CD4+T lymphocytes with an IC50 value of 265 nM.
RO2959 is a potent SOCE inhibitor that blocks an IP3-dependent current in CRAC-expressing RBL-2H3 cells and CHO cells stably expressing human Orai1 and Stim1, as well as SOCE in human primary CD4 T cells triggered by either T cell receptor (TCR) stimulation or thapsigargin treatment. RO2959 completely inhibits cytokine production as well as T cell proliferation mediated by TCR stimulation or MLR (mixed lymphocyte reaction). 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
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]. Gang Chen, et al. Characterization of a Novel CRAC Inhibitor That Potently Blocks Human T Cell Activation and Effector Functions. Mol Immunol. 2013 Jul;54(3-4):355-67.
[2]. Changbo Zheng, et al. Gastrodin Inhibits Store-Operated Ca 2+ Entry and Alleviates Cardiac Hypertrophy. Front Pharmacol. 2017 Apr 25;8:222.
溶解度数据
In Vitro: DMSO : 25 mg/mL (53.89 mM; Need ultrasonic)H2O : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble)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。

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