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SC-58125 是一种选择性的环氧合酶2 (COX-2)的抑制剂,IC50值为 0.04 μM。它在体内外均表现出抗肿瘤活性,还可抑制炎症部位的水肿并具有缓解疼痛作用。
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SC-58125 是一种选择性的环氧合酶2 (COX-2)的抑制剂,IC50值为 0.04 μM。它在体内外均表现出抗肿瘤活性,还可抑制炎症部位的水肿并具有缓解疼痛作用。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 147 | 现货 | |
2 mg | ¥ 198 | 现货 | |
5 mg | ¥ 347 | 现货 | |
10 mg | ¥ 588 | 现货 | |
25 mg | ¥ 1,090 | 现货 | |
50 mg | ¥ 1,630 | 现货 | |
100 mg | ¥ 2,350 | 现货 | |
200 mg | ¥ 3,360 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 458 | 现货 |
产品描述 | SC-58125 is a selective cyclooxygenase 2 (COX-2) inhibitor, with an IC50 of 0.04 μM. SC-58125 exhibits antitumor activity in vitro and in vivo, and it also can inhibit edema at the inflammatory site and is analgesic |
靶点活性 | COX-2:0.04 μM |
体外活性 | SC-58125 treatment on the growth of human colon carcinoma cells in nude mice.?Delaying treatment by 2, 4, or 7 weeks following implantation of the carcinoma cells resulted in a significant inhibition of tumor growth.?Furthermore, short-term (48 hours) treatment with SC-58125 was sufficient to attenuate tumor growth for up to 15 days.?SC-58125 treatment did not alter the rate at which cells underwent apoptosis, but did result in a delayed progression through the cell cycle at the G(2)/M transition.?Accordingly, p34(cdc2) protein levels and activity were decreased following SC-58125 treatment.SC-58125 primarily exerts a cytostatic effect in vivo, which is likely to be mediated through inhibition of progression through the G(2)/M phase of the cell cycle |
别名 | SC 58125, 1-[(4-甲基磺酰基)苯基]-3-三氟甲基-5-(4-氟苯基)吡唑 |
分子量 | 384.35 |
分子式 | C17H12F4N2O2S |
CAS No. | 162054-19-5 |
Smiles | CS(=O)(=O)c1ccc(cc1)-n1nc(cc1-c1ccc(F)cc1)C(F)(F)F |
密度 | 1.41g/cm3 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||
溶解度信息 | DMSO: 9 mg/mL (23.42 mM) | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
DMSO
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