3,4-二氟-N-(吡啶-4-基甲基)苯磺酰胺结构式
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常用名 | 3,4-二氟-N-(吡啶-4-基甲基)苯磺酰胺 | 英文名 | Schnurri-3 inhibitor-1 |
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| CAS号 | 736154-60-2 | 分子量 | 284.28 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C12H10F2N2O2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
3,4-二氟-N-(吡啶-4-基甲基)苯磺酰胺用途Schnurri-3抑制剂-1是一种有效的Schnurry-3抑制剂,是成人骨形成的重要调节器。Schnurri-3抑制剂-1可通过EF1alpha启动子抑制成骨细胞系Shn3FFL中的Shn3,AC50值为2.09μM。Schnurri-3抑制剂-1可用于研究骨质疏松症[1]。 |
| 中文名 | 3,4-二氟-N-(吡啶-4-基甲基)苯磺酰胺 |
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| 英文名 | Benzenesulfonamide, 3,4-difluoro-N-(4-pyridinylmethyl) |
| 描述 | Schnurri-3抑制剂-1是一种有效的Schnurry-3抑制剂,是成人骨形成的重要调节器。Schnurri-3抑制剂-1可通过EF1alpha启动子抑制成骨细胞系Shn3FFL中的Shn3,AC50值为2.09μM。Schnurri-3抑制剂-1可用于研究骨质疏松症[1]。 |
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| 相关类别 | |
| 靶点实验 |
Schnurri-3[1] |
| 体外研究 | Schnurri-3抑制剂-1(0-50μM;24小时)可以在SV40大T抗原转化成骨细胞系(Clone20-Shn3FFL)中用EF1alpha启动子抑制Shn3,AC50值为2.09μM[1]。Schnurri-3抑制剂-1(0.195-26μM;48 h)在HepG2哺乳动物细胞中表现出中等活性,AC50值为54.73μM[1]。细胞活力测定[1]细胞株:Clone20-Shn3FFL细胞浓度:2.09μM培养时间:24小时结果:显示活性浓度AC50值为2.09μM。细胞活力测定[1]细胞株:Clone20-Shn3FFL细胞浓度:1.2μM培养时间:24小时结果:显示活性浓度AC50值为1.2μM。 |
| 参考文献 |
[1]. National Center for Biotechnology Information. PubChem Compound Summary for CID 2473445. |
| 分子式 | C12H10F2N2O2S |
|---|---|
| 分子量 | 284.28 |
| InChIKey | BMPWOBNXZUHLQC-UHFFFAOYSA-N |
| SMILES | O=S(=O)(NCc1ccncc1)c1ccc(F)c(F)c1 |
| 储存条件 | 2-8°C, 干燥 |
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