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Naproxen is a COX-1 and COX-2 inhibitor (IC50s: 8.72 and 5.15 μM, respectively in cell assay). Naproxen etemesil is a lipophilic and non-acidic prodrug of naproxen. It is hydrolyzed to pharmacologically active Naproxen once absorbed.
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Naproxen is a COX-1 and COX-2 inhibitor (IC50s: 8.72 and 5.15 μM, respectively in cell assay). Naproxen etemesil is a lipophilic and non-acidic prodrug of naproxen. It is hydrolyzed to pharmacologically active Naproxen once absorbed.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
2 mg | ¥ 1,170 | 5日内发货 | |
5 mg | ¥ 1,980 | 5日内发货 | |
25 mg | ¥ 8,620 | 6-8周 | |
50 mg | ¥ 11,200 | 6-8周 | |
100 mg | ¥ 16,200 | 6-8周 | |
1 mL x 10 mM (in DMSO) | ¥ 2,280 | 5日内发货 |
产品描述 | Naproxen is a COX-1 and COX-2 inhibitor (IC50s: 8.72 and 5.15 μM, respectively in cell assay). Naproxen etemesil is a lipophilic and non-acidic prodrug of naproxen. It is hydrolyzed to pharmacologically active Naproxen once absorbed. |
靶点活性 | COX-2:5.15 μM, COX-1:8.72 μM |
体外活性 | Naproxen is a well known nonsteroidal anti-inflammatory drug. Naproxen is an approximately equipotent inhibitor of COX-1 and COX-2 in intact cells (IC50s: 2.2 μg/mL and 1.3 μg/mL, respectively)[1]. |
体内活性 | Naproxen is shown to inhibit the time-courses of pain, fever, and PGE2 with similar potencies (IC50=27, 40, 13 μM). Naproxen exerts an anti-inflammatory and antifibrotic effect in the mouse model of bleomycin-induced lung fibrosis. Naproxen also downregulates TGF-β levels and Smad3/4 complex formation [2][3]. |
别名 | MX 1094, LT-NS 001 |
分子量 | 336.4 |
分子式 | C17H20O5S |
CAS No. | 385800-16-8 |
密度 | 1.238 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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