CAS NO: | 56121-42-7 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
生物活性 | Aurantiamide acetate (TMC-58A) is a selective and orally activecathepsininhibitor isolated from Portulaca oleraceaL. Aurantiamide acetate has anti-inflammatory activities and can be used for the study of inflammatory diseases[1][2]. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | Aurantiamide acetate inhibits cathepsin L (3.4.22.15) and cathepsin B (3.4.22.1) with IC50 of 12 μM and 49 μM, respectiveiy[1]. | ||||||||||||||||
分子量 | 444.52 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C27H28N2O4 | ||||||||||||||||
CAS 号 | 56121-42-7 | ||||||||||||||||
结构分类 |
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来源 |
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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 : 50 mg/mL(112.48 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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