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HDAC-IN-7 是 Tucidinostat (Chidamide) 的类似物,是一种 HDAC 抑制剂。HDAC-IN-7 通过抑制组蛋白 H3 的乙酰化作用,诱导人类结肠癌细胞系的凋亡[1]。

HDAC-IN-7 是 Tucidinostat (Chidamide) 的类似物,是一种 HDAC 抑制剂。HDAC-IN-7 通过抑制组蛋白 H3 的乙酰化作用,诱导人类结肠癌细胞系的凋亡[1]。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 738 | 现货 | |
| 2 mg | ¥ 1,080 | 现货 | |
| 5 mg | ¥ 1,610 | 现货 | |
| 10 mg | ¥ 2,820 | 现货 | |
| 25 mg | ¥ 4,690 | 现货 | |
| 50 mg | ¥ 6,690 | 现货 | |
| 100 mg | ¥ 8,910 | 现货 | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,710 | 现货 |
HDAC-IN-7 相关产品
| 产品描述 | HDAC-IN-7, an analogue of Tucidinostat (Chidamide), is a HDAC inhibitor. HDAC-IN-7 inhibits acetylation of histone protein H3 and induces apoptosis in human colon cancer cell lines[1]. |
| 靶点活性 | HDAC3:67nM, HDAC11:432 nM, HDAC2:160nM, HDAC8:733nM, HDAC10:78 nM, HDAC1:95nM |
| 分子量 | 390.41 |
| 分子式 | C22H19FN4O2 |
| CAS No. | 743420-02-2 |
| Smiles | N(C(=O)C1=CC=C(CNC(C=CC=2C=CC=NC2)=O)C=C1)C3=C(N)C=CC(F)=C3 |
| 密度 | 1.336 g/cm3 (Predicted) |
| 颜色 | Brown |
| 物理性状 | Solid |
| 存储 | keep away from direct sunlight | 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: 55 mg/mL (140.88 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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DMSO
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