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描述 | Synta66 is an inhibitor of Orai. At a concentration of 10 μM, Synta66 attenuates the SOCE peak of Müller's glia[1].At 10 μM, Synta66 almost completely blocks Ca2+ entry signals induced by CaCl2 addition, and in platelets moderately reduces Ca2+ mobilisation from stores by 10%-30%. Synta66 inhibits plasma human platelet activation and whole blood thrombosis. Synta66 also inhibits platelet reactions and thrombosis in mice[2].Synta66 (10 μM) inhibited the LAD2 human mast cell line, significantly inhibited FcεRI-stimulated histamine and TNFα secretion, and differentially affected FcεRI-stimulated prostaglandin D2 and cytokine release[3]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.84mL 0.57mL 0.28mL |
14.19mL 2.84mL 1.42mL |
28.38mL 5.68mL 2.84mL |
CAS号 | 835904-51-3 |
分子式 | C20H17FN2O3 |
分子量 | 352.359 |
别名 | |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry,2-8°C |
溶解方案 |
DMSO: 80 mg/mL(227.04 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的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,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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动物实验配方 |