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ZED-1227 (TAK-227) 是一种具有口服活性、选择性和高效性的转谷氨酰胺酶 2 (TG2) 抑制剂,具有抗癌活性,能阻塞炎症诱导的 TG2 表达和激活,可用于治疗乳糜泻。
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ZED-1227 (TAK-227) 是一种具有口服活性、选择性和高效性的转谷氨酰胺酶 2 (TG2) 抑制剂,具有抗癌活性,能阻塞炎症诱导的 TG2 表达和激活,可用于治疗乳糜泻。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 2,890 | 现货 | |
5 mg | ¥ 6,490 | 现货 | |
10 mg | ¥ 8,750 | 现货 | |
25 mg | ¥ 12,900 | 现货 | |
50 mg | ¥ 17,500 | 现货 | |
100 mg | ¥ 23,600 | 现货 |
产品描述 | ZED-1227 (TAK-227) is an orally active, selective and potent transglutaminase 2 (TG2) inhibitor with anticancer activity that blocks inflammation-induced TG2 expression and activation for the treatment of Celiac Disease. |
靶点活性 | TGase 2:45 nM |
体外活性 | ZED-1227, at concentrations ranging from 0.1 μM to 1 μM for 24 hours, does not impact metabolic activity and proliferation in Huh7 cells and CaCo2 cells. This lack of effect suggests that ZED-1227 does not exhibit cytotoxic activity[1]. In an in vitro setting, ZED-1227, when applied at concentrations between 0.002 and 0.2 mg/mL for 30 minutes, inhibits transglutaminase 2 (TG2) in the small intestinal mucosa[1]. |
体内活性 | In mice, ZED-1227 reduces the activity of intestinal TG2 induced by Polyinosinic:Polycytidylic acid (40 mg/kg) to levels comparable to normal control levels. Additionally, ZED-1227 administration subdues intestinal inflammation in these mice[1].Furthermore, when administered orally (5 mg/kg; i.g.), ZED-1227 is effective in inhibiting TG2 in the small intestinal mucosa[1]. |
别名 | ZED-101, TAK-227 |
分子量 | 528.6 |
分子式 | C26H36N6O6 |
CAS No. | 1542132-88-6 |
存储 | store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 100 mg/mL (189.18 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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