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Fingolimod (FTY-720A) 是一种 1-磷酸鞘氨醇 (S1P) 拮抗剂,作用于 K562 和 NK 细胞,IC50为 0.033 nM。它还是pak1激活剂和免疫抑制剂。
Fingolimod (FTY-720A) 是一种 1-磷酸鞘氨醇 (S1P) 拮抗剂,作用于 K562 和 NK 细胞,IC50为 0.033 nM。它还是pak1激活剂和免疫抑制剂。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
100 mg | ¥ 457 | 现货 | |
500 mg | ¥ 1,255 | 现货 | |
1 g | ¥ 1,570 | 现货 |
产品描述 | Fingolimod (FTY-720A) is an antagonist of sphingosine 1-phosphate (S1P) (IC50 of 0.033 nM in K562 and NK cells). |
靶点活性 | S1P1:0.033 nM |
体外活性 | Fingolimod通过抑制溶血磷脂酶自噬毒素来降低LPA合成。Fingolimod治疗与轴突cAMP的显著增加相关,这对于轴突生长至关重要。此外,Fingolimod显著减少了受伤神经中的LPA水平。PF-8380治疗与髓鞘厚度的改善相关[1]。 |
细胞实验 | Sciatic nerve crush was performed in wildtype C57BL/6, in immunodeficient Rag1 (-/-) and Foxn1 (-/-) mice.?Analyses were based on walking track analysis and electrophysiology, histology, and cAMP formation.?Quantification of different LPA species was performed by liquid chromatography coupled to tandem mass spectrometry.?Furthermore, functional consequences of autotaxin inhibition by the specific inhibitor PF-8380 and the impact of fingolimod on early cytokine release in the injured sciatic nerve were investigated[1]. |
别名 | 芬戈莫德, FTY-720A, FTY-720, 2-氨基-2-[2-(4-辛基苯基)乙基]-1,3-丙二醇 |
分子量 | 307.47 |
分子式 | C19H33NO2 |
CAS No. | 162359-55-9 |
存储 | keep away from direct sunlight,store at low temperature,store under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | Methanol: 30 mg/mL (97.57 mM), Sonication is recommended. Ethanol: 7.69 mg/mL (25.01 mM), Sonication is recommended. DMSO: 1 mg/ml, Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
Ethanol/Methanol
Methanol
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