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AS1949490 是选择性SHIP-2抑制剂,其IC50=620 nM。它能够通过上调L6肌管GLUT1基因激活葡萄糖代谢。


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AS1949490 是选择性SHIP-2抑制剂,其IC50=620 nM。它能够通过上调L6肌管GLUT1基因激活葡萄糖代谢。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 413 | In stock | |
| 5 mg | ¥ 892 | In stock | |
| 10 mg | ¥ 1,480 | In stock | |
| 25 mg | ¥ 3,150 | In stock | |
| 50 mg | ¥ 4,570 | In stock | |
| 100 mg | ¥ 6,380 | In stock | |
| 200 mg | ¥ 8,630 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 745 | In stock |
AS1949490 相关产品
| 产品描述 | AS1949490 activated glucose metabolism via up-regulation of GLUT1 gene in L6 myotubes[1][2]. AS1949490 is a potent and selective SHIP-2 (SH2 domain-containing inositol 5′ phosphatase 2) inhibitor, with an IC50 of 620 nM. |
| 靶点活性 | SHIP2:620 nM |
| 分子量 | 371.88 |
| 分子式 | C20H18ClNO2S |
| CAS No. | 1203680-76-5 |
| Smiles | C[C@H](NC(=O)c1sccc1OCc1ccc(Cl)cc1)c1ccccc1 |
| 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 | DMSO: 49 mg/mL (131.76 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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DMSO
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