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(E)-SI-2 是类固醇受体 coactivator-3(SRC-3 或 AIB1)的有效小分子抑制剂,可选择性抑制 SRC-3 的内在转录活性,也抑制 SRC-1 和 SRC-2。它选择性地降低 SRC-3 的细胞蛋白水平,但不降低 CARM-1 的细胞蛋白水平,阻断 MDA-MB-468 细胞生长,IC50 值为 3.4 nM,但不影响正常细胞。

(E)-SI-2 是类固醇受体 coactivator-3(SRC-3 或 AIB1)的有效小分子抑制剂,可选择性抑制 SRC-3 的内在转录活性,也抑制 SRC-1 和 SRC-2。它选择性地降低 SRC-3 的细胞蛋白水平,但不降低 CARM-1 的细胞蛋白水平,阻断 MDA-MB-468 细胞生长,IC50 值为 3.4 nM,但不影响正常细胞。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 546 | 现货 | |
| 5 mg | ¥ 1,220 | 现货 | |
| 10 mg | ¥ 1,810 | 现货 | |
| 25 mg | ¥ 2,880 | 现货 | |
| 50 mg | ¥ 3,910 | 现货 | |
| 100 mg | ¥ 5,250 | 现货 | |
| 200 mg | ¥ 6,900 | 现货 | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,230 | 现货 |
| 产品描述 | (E)-SI-2 is a potent small-molecule inhibitor of steroid receptor coactivator-3 (SRC-3 or AIB1) that can selectively inhibit the intrinsic transcriptional activities of SRC-3, also inhibits SRC-1 and SRC-2. It selectively reduces cellular protein levels of SRC-3, but not that of CARM-1, blocks MDA-MB-468 cell growth with an IC50 value of 3.4 nM, but spares normal cells. |
| 分子量 | 265.31 |
| 分子式 | C15H15N5 |
| CAS No. | 380537-35-9 |
| Smiles | CN1C=2C(N=C1N/N=C(\C)/C3=CC=CC=N3)=CC=CC2 |
| 密度 | 1.22 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: 50 mg/mL (188.46 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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DMSO
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