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PF-543 Citrate (Sphingosine Kinase 1 Inhibitor II Citrate) 是一种具有选择性和高效性的鞘氨醇激酶 1 (SPHK1)抑制剂,也是高效性的 1-磷酸鞘氨醇 (S1P) 形成抑制剂,具有抗癌、抗纤维化和抗炎活性,可用于研究直肠癌。

PF-543 Citrate (Sphingosine Kinase 1 Inhibitor II Citrate) 是一种具有选择性和高效性的鞘氨醇激酶 1 (SPHK1)抑制剂,也是高效性的 1-磷酸鞘氨醇 (S1P) 形成抑制剂,具有抗癌、抗纤维化和抗炎活性,可用于研究直肠癌。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 2 mg | ¥ 323 | In stock | |
| 5 mg | ¥ 519 | In stock | |
| 10 mg | 待询 | In stock | |
| 25 mg | 待询 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 799 | In stock |
PF-543 Citrate 相关产品
| 产品描述 | PF-543 Citrate (Sphingosine Kinase 1 Inhibitor II Citrate) is a selective and potent inhibitor of sphingosine kinase 1 (SPHK1) and is an efficient inhibitor of 1-phosphate sphingosine (S1P) formation. It possesses anticancer, antifibrotic, and anti-inflammatory activities and can be used in research on colorectal cancer. |
| 靶点活性 | S1P:26.7 nM, SPHK1:3.6 nM (Ki), SPHK1:2 nM |
| 体外活性 | PF-543 Citrate 是一种选择性的鞘氨醇竞争性 SPHK1 抑制剂,IC50 为 2 nM,Ki 为 3.6 nM。 |
| 体内活性 | 在肺动脉高压的小鼠缺氧模型中施用 PF-543 Citrate (1 mg/kg,腹膜内注射,每隔一天,持续 21 天) ,对血管重塑没有影响,但减少了右心室肥大。 |
| 别名 | Sphingosine Kinase 1 Inhibitor II Citrate, PF543 Citrate |
| 分子量 | 657.73 |
| 分子式 | C33H39NO11S |
| CAS No. | 1415562-83-2 |
| Smiles | C(CC(O)=O)(CC(O)=O)(C(O)=O)O.C(N1[C@@H](CO)CCC1)C2=CC=C(COC3=CC(CS(=O)(=O)C4=CC=CC=C4)=CC(C)=C3)C=C2 |
| 密度 | no data available |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||||||||||||
| 溶解度信息 | H2O: 40 mg/mL (60.82 mM), Sonication is recommended. DMSO: 80 mg/mL (121.63 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
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H2O/DMSO
DMSO
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