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HDAC3-IN-6 (Compound SC26) 是一种选择性HDAC3抑制剂,其IC50为53 nM。它能够剂量依赖性地诱导PD-L1表达,并且引起显著的细胞凋亡 (Apoptosis) 和ROS生成。HDAC3-IN-6 在结直肠癌中展现出较高的抗肿瘤活性。

HDAC3-IN-6 (Compound SC26) 是一种选择性HDAC3抑制剂,其IC50为53 nM。它能够剂量依赖性地诱导PD-L1表达,并且引起显著的细胞凋亡 (Apoptosis) 和ROS生成。HDAC3-IN-6 在结直肠癌中展现出较高的抗肿瘤活性。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
HDAC3-IN-6 相关产品
| 产品描述 | HDAC3-IN-6 (Compound SC26) is a selective HDAC3 inhibitor with an IC50 of 53 nM. It induces PD-L1 expression in a dose-dependent manner and leads to significant apoptosis and reactive oxygen species (ROS) production. HDAC3-IN-6 exhibits strong antitumor efficacy against colorectal cancer. |
| 靶点活性 | HDAC3:53 nM |
| 分子量 | 417.46 |
| 分子式 | C23H23N5O3 |
| 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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