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Branaplam (LMI070; NVS-SM1) hydrochloride 是一种选择性、口服活性的 SMN2 剪接调节剂,能够直接作用于 SMN,其 EC50 值为 20 nM。Branaplam hydrochloride 还可抑制 hERG 通道,其 IC50 值为 6.3 μM。在严重脊髓性肌萎缩症(SMA)小鼠模型中,Branaplam hydrochloride 显著增加了全长 SMN 蛋白水平,并明显延长了生存期。

Branaplam (LMI070; NVS-SM1) hydrochloride 是一种选择性、口服活性的 SMN2 剪接调节剂,能够直接作用于 SMN,其 EC50 值为 20 nM。Branaplam hydrochloride 还可抑制 hERG 通道,其 IC50 值为 6.3 μM。在严重脊髓性肌萎缩症(SMA)小鼠模型中,Branaplam hydrochloride 显著增加了全长 SMN 蛋白水平,并明显延长了生存期。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 477 | In stock | |
| 5 mg | ¥ 1,070 | In stock | |
| 10 mg | ¥ 1,730 | In stock | |
| 25 mg | ¥ 2,890 | In stock | |
| 50 mg | ¥ 3,970 | In stock | |
| 100 mg | ¥ 5,790 | In stock | |
| 200 mg | ¥ 7,820 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 987 | In stock |
Branaplam hydrochloride 相关产品
| 产品描述 | Branaplam hydrochloride (LMI070; NVS-SM1) is a selective and orally active SMN2 splicing modulator that acts directly on SMN with an EC50 value of 20 nM. Branaplam hydrochloride also inhibits hERG channels, demonstrating an IC50 of 6.3 μM. In a mouse model of severe spinal muscular atrophy (SMA), Branaplam hydrochloride significantly increased full-length SMN protein levels and markedly improved survival. |
| 靶点活性 | ERG (human):6.3 μM, SMN:20 nM (EC50) |
| 体外活性 | 在人类成纤维细胞中,Branaplam hydrochloride 引起了175个基因表达水平的改变。[1] |
| 体内活性 | 经口服给予Branaplam hydrochloride (3、10、30 mg/kg) 后,小鼠脑和脊髓中的SMN2-FL转录本及SMN蛋白水平呈现出剂量依赖性的升高 [1]。 |
| 别名 | 布拉扑兰盐酸盐, NVS-SM1 hydrochloride, LMI070 hydrochloride, LMI 070 hydrochloride |
| 分子量 | 429.95 |
| 分子式 | C22H28ClN5O2 |
| CAS No. | 1562338-39-9 |
| Smiles | Cl.OC1=CC(=CC=C1C=2N=NC(OC3CC(NC(C)(C)C3)(C)C)=CC2)C=4C=NNC4 |
| 颜色 | Yellow |
| 物理性状 | Solid |
| 存储 | keep away from moisture,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 | H2O: <1mg/mL (Insoluble) DMSO: 200 mg/mL (465.17 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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