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Tenidap (CP-66248) 是选择性的 COX-1 和SLC26A3 抑制剂,具有具有抗炎,镇痛和抗风湿活性,抑制 COX-1 和COX-2 ,可抑制 DNA 和胶原蛋白的合成,抑制细胞增殖。

Tenidap (CP-66248) 是选择性的 COX-1 和SLC26A3 抑制剂,具有具有抗炎,镇痛和抗风湿活性,抑制 COX-1 和COX-2 ,可抑制 DNA 和胶原蛋白的合成,抑制细胞增殖。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 328 | In stock | |
| 2 mg | ¥ 443 | In stock | |
| 5 mg | ¥ 662 | In stock | |
| 10 mg | ¥ 1,120 | In stock | |
| 25 mg | ¥ 2,370 | In stock | |
| 50 mg | ¥ 3,530 | In stock | |
| 100 mg | ¥ 4,970 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 728 | In stock |
Tenidap 相关产品
| 产品描述 | Tenidap (CP-66248) is a selective COX-1 and SLC26A3 inhibitor with anti-inflammatory, analgesic, and anti-rheumatic activities. |
| 靶点活性 | COX-1:0.03 μM, COX-2:1.2 μM |
| 体外活性 | The human astrocytoma cell line U373 MG was incubated with 0.1-100 µM tenidap for 30 min and then stimulated with 50 µM C6-ceramide for 24 h. Tenidap inhibited the dose-dependent ceramide-induced IL-6 protein synthesis in U373 human astrocytoma cells.[4] |
| 体内活性 | 雄性Wistar大鼠在三氯司他汀诱导的持续性癫痫(SE)后,每天10毫克/公斤的剂量给药10天,Tenidap-SE组存活46.88±10.70个神经元,Tenidap-SE组存活37.75±8.78个神经元,Tenidap显著抑制了COX-2在海马尤其是CA3区的表达[3]。 |
| 别名 | 替尼达普, CP-66248 |
| 分子量 | 320.75 |
| 分子式 | C14H9ClN2O3S |
| CAS No. | 120210-48-2 |
| Smiles | NC(=O)N1C(=O)\C(=C(/O)c2cccs2)c2cc(Cl)ccc12 |
| 密度 | 1.648 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: 20 mg/mL (62.35 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
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