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Z57346765是一种特异性的PGK1(Phosphoglycerate kinase 1)抑制剂,通过降低糖酵解过程中PGK1的代谢酶活性,抑制PGK1依赖的细胞增殖。临床期中,Z57346765对局部晚期肾透明细胞癌(KIRC)具有剂量依赖的抑制作用,通过诱导与细胞代谢、DNA复制以及细胞周期相关的基因表达发生变化。
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Z57346765是一种特异性的PGK1(Phosphoglycerate kinase 1)抑制剂,通过降低糖酵解过程中PGK1的代谢酶活性,抑制PGK1依赖的细胞增殖。临床期中,Z57346765对局部晚期肾透明细胞癌(KIRC)具有剂量依赖的抑制作用,通过诱导与细胞代谢、DNA复制以及细胞周期相关的基因表达发生变化。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 447 | 10-14周 | |
5 mg | ¥ 1,080 | 10-14周 | |
10 mg | ¥ 1,630 | 10-14周 | |
25 mg | ¥ 3,260 | 10-14周 | |
50 mg | ¥ 4,890 | 10-14周 | |
100 mg | ¥ 6,780 | 10-14周 | |
200 mg | ¥ 9,130 | 10-14周 |
产品描述 | Z57346765 is a specific PGK1(Phosphoglycerate kinase 1) inhibitor that inhibits PGK1-dependent cell proliferation by decreasing the metabolic enzyme activity of PGK1 during glycolysis. In the clinical phase, Z57346765 had a dose-dependent inhibitory effect on locally advanced renal clear cell carcinoma (KIRC) by inducing changes in the expression of genes related to cell metabolism, DNA replication, and the cell cycle. |
别名 | Z 57346765 |
分子量 | 294.35 |
分子式 | C17H18N4O |
CAS No. | 1016340-64-9 |
存储 | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 80 mg/mL (271.79 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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