Synta66
目录号: PL01886 纯度: ≥99%
CAS No. :835904-51-3
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中文名称
Synta66
中文别名
化合物SYNTA66
英文名称
Synta66
英文别名
4-PYRIDINECARBOXAMIDE, N-(2',5'-DIMETHOXY[1,1'-BIPHENYL]-4-YL)-3-FLUORO-;4-Pyridinecarboxamide, N-(2′,5′-dimethoxy[1,1′-biphenyl]-4-yl)-3-fluoro-;GSK1349571A;N-(2′,5′-Dimethoxy[1,1′-biphenyl]-4-yl)-3-fluoro-4-pyridinecarboxamide;S66;Synta 66;Synta-66;Synta66;4-Pyridinecarboxamide, N-(2',5'-dimethoxy[1,1'-biphenyl]-4-yl)-3-fluoro-
Cas No.
835904-51-3
分子式
C20H17N2O3F
分子量
352.36
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Synta66 是钙离子通道 Orai (CRAC 的核心) 的抑制剂,主要用于神经疾病的研究。
生物活性
Synta66 is an inhibitor of store-operated calcium entry channel Orai, which forms the pore of the CRAC channel, and used for the research of neurological disease.
性状
Solid
IC50 & Target[1][2]
Orai
体外研究(In Vitro)
Synta66 is an inhibitor of Orai, which forms the pore of the CRAC channel. Synta66 (10 μM) attenuates peak SOCE in Müller glia. Synta66 (10 μM) prevents orai channels mediating the residual SOC current in Trpc1 Müller cells. Synta66 (10 μM) nearly completely blocks the Ca entry signal evoked by CaCl2 addition, whereas it moderately reduces Ca mobilization from stores with 10% to 30% in platelet. Synta66 (10 μM) suppresses human platelet activation in plasma and whole-blood thrombus formation. Synta66 (10 μM) also inhibits murine platelet responses and thrombus formation. Synta66 (10 μM) inhibits LAD2 human mast cell line. Synta66 (10 μM) significantly inhibits FcεRI stimulated histamine and TNFα secretion, and has differential effects on FcεRI stimulated prostaglandin D2 and cytokine release in human lung mast cells (HLMCs).
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]. Molnár T, et al. Store-Operated Calcium Entry in Müller Glia Is Controlled by Synergistic Activation of TRPC and Orai Channels. J Neurosci. 2016 Mar 16;36(11):3184-98.
[2]. van Kruchten R, et al. Antithrombotic potential of blockers of store-operated calcium channels in platelets. Arterioscler Thromb Vasc Biol. 2012 Jul;32(7):1717-23.
溶解度数据
In Vitro: DMSO : 77.5 mg/mL (219.95 mM; Need ultrasonic)配制储备液
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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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