CAS NO: | 21256-18-8 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Oxaprozin is an orally active and potentCOXinhibitor, withIC50values of 2.2 μM for human plateletCOX-1and and 36 μM for IL-1-stimulated human synovial cellCOX-2, respectively. Oxaprozin also inhibits the activation ofNF-κB. Oxaprozin induces cellapoptosis. Oxaprozin shows anti-inflammatory activity. Oxaprozin-mediated inhibition of theAkt/IKK/NF-κBpathway contributes to its anti-inflammatory properties[1][2]. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | Oxaprozin induces apoptosis in a dose-dependent manner. Oxaprozin increases caspase-3 activity in the activated but not in the resting condition. NF-κB activation is inhibited by Oxaprozin (50 μM). Oxaprozin inhibits activation of the IKK system induced by the reagent IκBα[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 293.32 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C18H15NO3 | ||||||||||||||||
CAS 号 | 21256-18-8 | ||||||||||||||||
中文名称 | 奥沙普秦;恶丙嗪 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : ≥ 100 mg/mL(340.92 mM) *"≥" means soluble, but saturation unknown. 配制储备液
* 请根据半岛bd体育手机客户端
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半岛bd体育手机客户端
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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