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TRPM7-IN-1(compound SUD)为苯甲酰脲衍生物,具备有效抑制TRPM7的特性。该化合物在MCF-7和BGC-823细胞中引发细胞周期停滞及促进细胞凋亡,有效减缓细胞迁移速度。TRPM7-IN-1减少波形蛋白的表达,同时增强E-钙粘蛋白的表达,下调TRPM7样电流,并通过激活PI3K/Akt信号通路减少TRPM7表达。此外,TRPM7-IN-1作为一种潜在药物,通过抑制TRPM7的表达与功能,有助于抑制乳腺癌和胃癌的转移。

TRPM7-IN-1(compound SUD)为苯甲酰脲衍生物,具备有效抑制TRPM7的特性。该化合物在MCF-7和BGC-823细胞中引发细胞周期停滞及促进细胞凋亡,有效减缓细胞迁移速度。TRPM7-IN-1减少波形蛋白的表达,同时增强E-钙粘蛋白的表达,下调TRPM7样电流,并通过激活PI3K/Akt信号通路减少TRPM7表达。此外,TRPM7-IN-1作为一种潜在药物,通过抑制TRPM7的表达与功能,有助于抑制乳腺癌和胃癌的转移。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 10-14周 | |
| 50 mg | 待询 | 10-14周 |
TRPM7-IN-1 相关产品
| 产品描述 | TRPM7-IN-1 (compound SUD) is a benzamide-urea derivative and an effective inhibitor of TRPM7. This compound induces cell cycle arrest and apoptosis in MCF-7 and BGC-823 cells, reducing their migration capabilities. It decreases vimentin expression while increasing E-cadherin expression. TRPM7-IN-1 reduces TRPM7-like currents and inhibits TRPM7 expression by activating the PI3K/Akt signaling pathway. This compound shows potential as a therapeutic agent for reducing breast and gastric cancer metastasis by targeting TRPM7 expression and activity. |
| 分子量 | 419.48 |
| 分子式 | C23H25N5O3 |
| CAS No. | 1909225-07-5 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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