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Cdc7-IN-1 纯度: 99.30%
Cdc7-IN-1 (Compound 13) 是一种高效、选择性的 ATP 竞争性的 Cdc7 激酶抑制剂,在 1 mM ATP 存在时对 Cdc7 作用的 IC50 值为 0.6 nM,具有解离率低的特质。Cdc7-IN-1 能高效地抑制癌细胞中的 Cdc7,诱导细胞死亡。

Cdc7-IN-1 Chemical Structure
CAS No. : 1402055-25-7
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥3850 | In-stock | |
5 mg | ¥3500 | In-stock | |
10 mg | ¥5500 | In-stock | |
50 mg | ¥16500 | In-stock | |
100 mg | ¥22500 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
* Please select Quantity before adding items.
Cdc7-IN-1 相关产品
•相关化合物库:
- Bioactive Compound Library Plus
- Cell Cycle/DNA Damage Compound Library
- Kinase Inhibitor Library
- Anti-Cancer Compound Library
- Anti-Aging Compound Library
- Anti-Breast Cancer Compound Library
- Anti-Blood Cancer Compound Library
生物活性 |
Cdc7-IN-1 (Compound 13) is a highly potent, selective and ATP competitive inhibitor of Cdc7 kinase, with an IC50 value of 0.6 nM at 1 mM ATP and with slow off-rate characteristics. Cdc7-IN-1 potently inhibits Cdc7 activity in cancer cells, and effectively induces cell death[1]. |
IC50 & Target |
IC50: 0.6 nM (Cdc7, at 1 mM ATP)[1] |
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分子量 |
409.82 |
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Formula |
C21H16ClN3O4 |
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CAS 号 |
1402055-25-7 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 5.2 mg/mL (12.69 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |
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参考文献 |
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