CAS NO: | 89197-00-2 |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Efaroxan hydrochloride is a potent, selective and orally activeα2-adrenoceptorantagonist, with antidiabetic activity. Efaroxan hydrochloride is a selectiveI1-Imidazoline receptorantagonist. Efaroxan hydrochloride can be used for the research ofcardiovascular disease[1][2][3]. | ||||||||||||||||
IC50& Target | α2-adrenoceptor, I1-Imidazoline receptor[1][2] | ||||||||||||||||
体外研究 (In Vitro) | Efaroxan hydrochloride binds to I1-imidazoline and α2-adrenergic receptors in bovine rostral ventrolateral medulla membranes, with Kis of 0.15 nM and 5.6 nM, respectively[1] | ||||||||||||||||
体内研究 (In Vivo) | Efaroxan hydrochloride increases plasma insulin levels in both conscious fed and fasted rats without greatly affecting plasma glucoselevels[3].
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分子量 | 252.74 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C13H17ClN2O | ||||||||||||||||
CAS 号 | 89197-00-2 | ||||||||||||||||
中文名称 | 盐酸盐依法克生 | ||||||||||||||||
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 : 50 mg/mL(197.83 mM;ultrasonic and warming and heat to 60℃) 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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