货号:A388367 同义名: Y-3642 HCl;Y-3642 hydrochloride
Tinoridine HCl is a nonsteroidal anti-inflammatory drug and also has potent radical scavenger and antiperoxidative activity.
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描述 | Active oxygen species have been implicated in a variety of pathophysiological conditions, such as inflammation, aging, hepatotoxicity and ischemic brain and myocardium damage. Tinoridine, a non-steroidal anti-inflammatory drug, inhibits the lipid peroxidation in rat liver microsomes and mitochondria. The anti-peroxidative activity of tinoridine has been suggested to contribute to its membrane stabilizing activity demonstrated on various biomembranes. Tinoridine reduced a stable free radical, diphenyl-p-picrylhydrazyl, in the molar ratio of about 1∶2, indicating its free radical scavenging ability. Tinoridine inhibited the lipid peroxidation in rat liver microsomes induced by xanthine-xanthine oxidase system in the presence of ADP and Fe2+, in which hydroxyl radical (•OH) is formed. These results indicate that tinoridine is able to scavenge •OH and the main active oxygen species responsible for the lipid peroxidation is •OH[1]. In addition, the administration of tinoridine (100 mg/kg) to rats prevented the CCl4-induced hepatotoxicity, in which the lipid peroxidation in microsomes caused by CC14 is suggested to have a decisive role[2]. |
NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
NCT01224756 | Pain Inflamma... 展开 >>tion 收起 << | Phase 4 | Completed | - | Indonesia ... 展开 >> Semarang, Central Java, Indonesia Jakarta, DKI Jakarta, Indonesia Surabaya, East Java, Indonesia Bandung, West Java, Indonesia 收起 << |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.83mL 0.57mL 0.28mL |
14.17mL 2.83mL 1.42mL |
28.34mL 5.67mL 2.83mL |
CAS号 | 25913-34-2 |
分子式 | C17H21ClN2O2S |
分子量 | 352.879 |
别名 | Y-3642 HCl;Y-3642 hydrochloride;Tinoridine hydrochloride |
运输 | 蓝冰 |
存储条件 |
粉末 Keep in dark place,Inert atmosphere,Room temperature 液体 -20°C:3-6个月-80°C:12个月 |
溶解度 |
DMSO: 16 mg/mL(45.34 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 2.5 mg/mL(7.08 mM),配合低频超声,并水浴加热至45℃助溶 |
动物实验配方 |