CAS NO: | 26171-23-3 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | Tolmetin is an orally active and potentCOXinhibitor withIC50s of 0.35 μM and 0.82 μM humanCOX-1andCOX-2, respectively. Tolmetin is a non-steroidal anti-inflammatory drug (NSAID)[1][2]. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | Tolmetin (0.25 mM) does not attenuate lipid peroxidation in rat brain homogenate. Tolmetin (0.25, 0.5, 0.75, 1 mM) shows radical scavenging properties but without superoxide anion generation in rat brain homogenat[3]. | ||||||||||||||||
体内研究 (In Vivo) | Tolmetin (30,100 mg/kg; gavage; single dose or twice daily for 3 and 14 days) shows maximal ulcerogenic effect 4 h after the single dose, while potently decreases after 3 and 14 days of repeated administration in male Wistar rats weighing 180-200 g. Tolmetin causes gastric lesions in 100 mg/kg[2]. | ||||||||||||||||
分子量 | 257.28 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C15H15NO3 | ||||||||||||||||
CAS 号 | 26171-23-3 | ||||||||||||||||
中文名称 | 托麦汀;托美丁 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 100 mg/mL(388.68 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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