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26993-30-6

中文名称 D-苏式-鞘胺醇-1-磷酸
英文名称 D-ERYTHRO-SPHINGOSINE-1-PHOSPHATE
CAS 26993-30-6
分子式 C18H38NO5P
MDL 编号 MFCD00274457
分子量 379.47
MOL 文件 26993-30-6.mol
更新日期 2024/01/22 13:00:57
26993-30-6 结构式 26993-30-6 结构式

基本信息

中文别名
D-苏式-鞘胺醇-1-磷酸
英文别名
1-SPP
D-ERYTHRO-DIHYDROSPHINGOSINE-1-PHOSPHATE
D-ERYTHRO-SPHINGOSINE-1-PHOSPHATE
(E)-D-ERYTHRO-2-AMINO-1-(DIHYDROGENPHOSPHATE)-4-OCTADECENE-1,3-DIOL
S1P
SPA
SPHINGOSINE-1-PHOSPHATE
SPHINGOSINE-1-PHOSPHATE, D-ERYTHRO
SPHINGOSINE-1-PHOSPHORIC ACID
SPHINGOSINE-1-PO4
SPN-1-P
SHINGOSINE-1-PHOSPHATE \ EDG-1 RECEPTOR
(2-amino-3-hydroxy-octadec-4-enoxy)phosphonic acid
1,3-Octadecanediol, 2-amino-, 1-(dihydrogen phosphate), D-erythro- (8C I)
所属类别
生物化工:生化试剂

物理化学性质

熔点179-189°C
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
储存条件-20°C
溶解度methanol: THF: water (6:3:1): >0.5 mg/mL
溶解度可溶于甲醇:四氢呋喃:水(6:3:1):>0.5 mg/mL
酸度系数(pKa)1.76±0.10(Predicted)
形态waxy solid
颜色yellow
敏感性感光
稳定性对水分、温度敏感;有吸湿性

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H315-H319-H335
危险品标志Xi
危险类别码36/37/38
危险类别码R36/37/38
安全说明26-36
安全说明S26-S36
WGK Germany3
WGK Germany3
海关编码29225090
DEA Controlled SubstancesCSCN: 1635
CAS SCH: IV
NARC: N

知名试剂公司产品信息

常见问题列表

生物活性
Sphingosine-1-phosphate (S1P) 是 S1P1-5 受体 (S1P1-5 receptors) 的激动剂和 GPR3、GPR6、GPR12 的配体。Sphingosine-1-phosphate 是细胞内的第二信使,动员 Ca2+ 作为 G 蛋白偶联受体的细胞外配体。Sphingosine-1-phosphate 是由鞘磷脂 (HY-113498) 或其他膜磷脂生成的重要脂质介质。
靶点

Human Endogenous Metabolite

体外研究

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).

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