| CAS: | 432001-69-9 | |
| 分子式: | C18H13BrN2O4S2 | |
| 分子量: | 465.34 | |
| 英文名称: |
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| 用途: | Skp2 inhibitor C1 (SKPin C1)是一种高选择性的Skp2-mediated p27 degradation小分子抑制剂。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||
| S873113 | MACKLIN | Skp2 inhibitor C1 (SKPin C1) | 99% | 729元/5mg; | 展开 | ||||||||||||||||||||||||||||||
储存:-20℃ 状态:粉末 | |||||||||||||||||||||||||||||||||||
| S797456 | MACKLIN | Skp2 inhibitor C1 (SKPin C1) | 10mM in DMSO | 648元/1ml; | 展开 | ||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||
| 5.00519 | Sigma-Aldrich | SKP2 E3 Ligase Inhibitor I, C1-CAS 432001-69-9-Calbiochem | 2417.18元/25 MG; | 展开 | |||||||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable rhodanine compound that upregulates cellular p21Cip1/Waf1 and p27Kip1 protein levels (10 µM for 16 h in 501 Mel cultures) by preventing Skp2-Cks1-mediated substrate recruitment without affecting the F-box E3 ubiquitin ligase Skp2 interaction with Cks1 or the SCF (Skp1-cullin1-F-box) complex. Shown to inhibit the proliferation of human breast cancer MCF-7 and melanoma 501 Mel cells (IC50 = 8 and 30 µM, respectively; 16 h incubation). Unlike SMIP004 (Cat. No. 500517), C1 does not affect cellular Cyclin E/CDK2 kinase activity or Skp2 level. 生化/生理作用 Cell permeable: yes 包装 Packaged under inert gas 警告 Toxicity: Standard Handling (A) 重悬 Use only fresh DMSO for reconstitution. 其他说明 Rico-Bautista, E., and Wolf, D.A. 2012. Chem. Biol.19, 1497. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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