CAS NO: | 26993-30-6 |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | Sphingosine-1-phosphate (S1P) is an agonist ofS1P1-5receptorsand a ligand of GPR3,GPR6and GPR12. Sphingosine-1-phosphate is an intracellular second messenger and mobilizes Ca2+as an extracellular ligand for G protein-coupled receptors[1]. Sphingosine-1-phosphate is an important lipid mediator generated from Sphingomyelin (HY-113498) or other membranephospholipids[2]. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | S1P (1 μM) induces a significant Ca2+releases in HEK293 cells under serum starvation conditions (1% FCS)[1].In a functional Ca2+assay, Suramin (HY-B0879) alone does not exert any effect on intracellular Ca2+release via gpr3, gpr6 or gpr12. In contrast, S1P (1 μM) induces Ca2+release of gpr3, gpr6 and gpr12 in the presence of Suramin (HY-B0879) various concentrations in transfected HEK293 cells[2].In a functional Ca2+assay,S1P (3-3000 nM) in the presence Suramin (300 μM), exhibits nanomolar EC50values for gpr3 (EC50=29 nM), gpr6 (EC50=15 nM) and gpr12 (EC50=24 nM), rat gpr3 (EC50=68 nM),respectively in HEK293 cells[2].S1P increases intracellular calcium levels in TAg-Jurkat cells expressing S1P1 and Gqi5, which allows for phospholipase C stimulation by Gi proteins, when used at a concentration of 200 nM, as well as in TAg-Jurkat cells expressing S1P2 and S1P3 receptors (EC50s = 8 and 11 nM, respectively)[3]. | ||||||||||||||||
分子量 | 379.47 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C18H38NO5P | ||||||||||||||||
CAS 号 | 26993-30-6 | ||||||||||||||||
结构分类 |
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运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | -20°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 5 mg/mL(13.18 mM;ultrasonic and warming and adjust pH to 4 with HCl and heat to 80℃) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |