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CP-10 is a PROTAC with highly selective and remarkable CDK6 degradation (DC50: 2.1 nM). It inhibits the proliferation of several hematopoietic cancer cells including multiple myeloma and can degrade mutated and overexpressed CDK6.

CP-10 is a PROTAC with highly selective and remarkable CDK6 degradation (DC50: 2.1 nM). It inhibits the proliferation of several hematopoietic cancer cells including multiple myeloma and can degrade mutated and overexpressed CDK6.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥ 7,320 | 待询 | |
| 10 mg | ¥ 10,300 | 待询 | |
| 50 mg | ¥ 21,900 | 待询 | |
| 100 mg | 待询 | 待询 | |
| 200 mg | 待询 | 待询 | |
| 1 mL x 10 mM (in DMSO) | ¥ 10,225 | 待询 |
| 产品描述 | CP-10 is a PROTAC with highly selective and remarkable CDK6 degradation (DC50: 2.1 nM). It inhibits the proliferation of several hematopoietic cancer cells including multiple myeloma and can degrade mutated and overexpressed CDK6. |
| 靶点活性 | CDK6:2.1 nM (Dc50), Cereblon: |
| 体外活性 | In human glioblastoma U251 cells, CP-10 induces nearly 72% degradation of CDK6 at 10 nM and 89% at 100 nM. The degradation of CDK4 induced by CP-10 is far weaker than that of CDK6 (DC50: 50-80 fold). CP-10 displays a cell inhibition potential in mantle cell lymphoma cells (in Mino, IC50≈8 nM) and multiple myeloma cell MM.1S (IC50≈10 nM). |
| 分子量 | 871.94 |
| 分子式 | C44H49N13O7 |
| CAS No. | 2366268-80-4 |
| Smiles | O=C1C=2C=CC=C(NCCOCCN3N=NC(=C3)CN4CCN(C5=CN=C(C=C5)NC=6N=CC7=C(N6)N(C(=O)C(C(=O)C)=C7C)C8CCCC8)CC4)C2C(=O)N1C9C(=O)NC(=O)CC9 |
| 密度 | 1.55 g/cm3 (Predicted) |
| 存储 | 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: 200 mg/mL (229.37 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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DMSO
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
对于不同动物的给药剂量换算,您也可以参考 更多