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PROTAC K-Ras Degrader-4是一种PROTAC分子,可以选择性降解致癌突变体K-Ras,在GP5d细胞系中有效降解KRASG12D,在SW620细胞中有效降解KRASG12V,DC50分别为1和13nM。PROTAC K-Ras Degrader-4同时抑制下游MAPK信号通路,这使其成为了了一种针对先前不可成药的Ras突变癌症的新研究策略。
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PROTAC K-Ras Degrader-4是一种PROTAC分子,可以选择性降解致癌突变体K-Ras,在GP5d细胞系中有效降解KRASG12D,在SW620细胞中有效降解KRASG12V,DC50分别为1和13nM。PROTAC K-Ras Degrader-4同时抑制下游MAPK信号通路,这使其成为了了一种针对先前不可成药的Ras突变癌症的新研究策略。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 1,300 | In stock | |
5 mg | ¥ 3,250 | In stock | |
10 mg | ¥ 4,730 | In stock | |
25 mg | ¥ 7,490 | In stock | |
50 mg | ¥ 9,870 | In stock |
PROTAC K-Ras Degrader-4 相关产品
产品描述 | PROTAC K-Ras Degrader-4 (Compound 4) is a proteolysis-targeting chimera (PROTAC) molecule designed to selectively degrade oncogenic mutants of K-Ras, effectively degrading KRASG12D in the GP5d cell line and KRASG12V in SW620 cells with DC50 of 1 nM and 13 nM, respectively; it concomitantly inhibits the downstream MAPK signaling pathway and represents a novel therapeutic strategy for cancer research targeting previously undruggable Ras mutations. |
体外活性 | PROTAC K-Ras Degrader-4(0-1 μM, 5 天)处理GP2d细胞系,发现其能抑制 DUSP6 的表达,并抑制 KRASG12D突变的 GP2d 细胞的增殖。[1] |
分子量 | 989.22 |
分子式 | C50H60N12O6S2 |
CAS No. | 2938169-99-2 |
密度 | no data available |
存储 | store at low temperature | 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: 80 mg/mL (80.87 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
DMSO
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