D-苏式-鞘胺醇-1-磷酸
D-苏式-鞘胺醇-1-磷酸 性质
熔点 | 179-189°C |
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沸点 | 548.8±60.0 °C(Predicted) |
密度 | 1.094±0.06 g/cm3(Predicted) |
RTECS号 | RG2260500 |
储存条件 | -20°C |
溶解度 | 可溶于甲醇:四氢呋喃:水(6:3:1):>0.5 mg/mL |
形态 | 蜡状固体 |
酸度系数(pKa) | 1.76±0.10(Predicted) |
颜色 | 粘黄色 |
敏感性 | Light Sensitive |
稳定性 | 对水分、温度敏感;有吸湿性 |
CAS 数据库 | 26993-30-6(CAS DataBase Reference) |
D-苏式-鞘胺醇-1-磷酸 用途与合成方法
Human Endogenous Metabolite
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S1P (1 μM) induces a significant Ca 2+ releases in HEK293 cells under serum starvation conditions (1% FCS).In a functional Ca 2+ assay, Suramin (HY-B0879) alone does not exert any effect on intracellular Ca 2+ release via gpr3, gpr6 or gpr12. In contrast, S1P (1 μM) induces Ca 2+ release of gpr3, gpr6 and gpr12 in the presence of Suramin (HY-B0879) various concentrations in transfected HEK293 cells. In a functional Ca 2+ assay,S1P (3-3000 nM) in the presence Suramin (300 μM), exhibits nanomolar EC 50 values for gpr3 (EC 50 =29 nM), gpr6 (EC 50 =15 nM) and gpr12 (EC 50 =24 nM), rat gpr3 (EC 50 =68 nM),respectively in HEK293 cells. S1P increases intracellular calcium levels in TAg-Jurkat cells expressing S1P1 and G qi5 , which allows for phospholipase C stimulation by G i proteins, when used at a concentration of 200 nM, as well as in TAg-Jurkat cells expressing S1P2 and S1P3 receptors (EC 50 s = 8 and 11 nM, respectively).
安全信息
危险品标志 | Xi |
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危险类别码 | 36/37/38 |
安全说明 | 26-36 |
WGK Germany | 3 |
海关编码 | 29225090 |
DEA Controlled Substances | CSCN: 1635 CAS SCH: IV NARC: N |
D-苏式-鞘胺醇-1-磷酸 价格(试剂级)
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
---|---|---|---|---|---|
2024-08-19 | 32852 | D-赤型神经胺磷酸盐 1MG | 26993-30-6 | 1mg | 3020 |
2024-08-19 | HY-108496 | 1 mg | 1890 |