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AGPS-IN-2i 是一种高效且具有很高亲和力的烷基甘油磷酸酯合成酶抑制剂的,可控制着细胞中醚脂的利用和代谢,降低了醚类脂质水平和细胞迁移率,促进癌细胞的增殖和运动。AGPS-IN-2i 在 PC-3和 MDA-MB-231癌细胞中测试时通过调节 E-cadherin、Snail 和 MMP2的表达水平,特异性地损害了上皮向间质转化(EMT)。AGPS-IN-2i 对癌细胞增殖具有抑制作用。
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AGPS-IN-2i 是一种高效且具有很高亲和力的烷基甘油磷酸酯合成酶抑制剂的,可控制着细胞中醚脂的利用和代谢,降低了醚类脂质水平和细胞迁移率,促进癌细胞的增殖和运动。AGPS-IN-2i 在 PC-3和 MDA-MB-231癌细胞中测试时通过调节 E-cadherin、Snail 和 MMP2的表达水平,特异性地损害了上皮向间质转化(EMT)。AGPS-IN-2i 对癌细胞增殖具有抑制作用。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 689 | 现货 | |
5 mg | ¥ 1,980 | 现货 | |
10 mg | ¥ 3,290 | 现货 | |
25 mg | ¥ 5,280 | 现货 | |
50 mg | ¥ 7,260 | 现货 | |
100 mg | ¥ 9,790 | 现货 | |
200 mg | ¥ 13,200 | 现货 |
产品描述 | AGPS-IN-2i is a potent and high-affinity inhibitor of alkylglycerol phosphate synthase that controls ether lipid utilization and metabolism in cells, reduces ether lipid levels and cell migration, and promotes proliferation and motility of cancer cells. AGPS-IN-2i had an inhibitory effect on cancer cell proliferation. |
体外活性 | AGPS-IN-2i (2i) (500 µM ; 24 h) reduced ether lipids levels and cell migration rate In 231MFP cancer cells.[1] 2i (50、100 µM ; 24 h) specifically impaired epithelial to mesenchymal transition (EMT) by modulating E-cadherin, Snail, and MMP2 expression levels in PC-3 and MDA-MB-231 cancer cells.[1] |
分子量 | 345.34 |
分子式 | C18H17F2N3O2 |
CAS No. | 2316782-88-2 |
存储 | store at low temperature | Shipping with blue ice. | ||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 22.5 mg/mL (65.15 mM) | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
DMSO
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