CAS NO: | 137417-08-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Dihydrexidine hydrochloride (DAR-0100 hydrochloride) is a high potent, selective and full efficacyD1-likedopamine receptor(D1/D5)agonist, with anIC50of 10 nM for D1 receptor. Dihydrexidine hydrochloride exhibits potent antiparkinsonian activity[1][2][3][4]. Dihydrexidine hydrochloride can stimulateYAPphosphorylation[5]. | ||||||||||||||||
IC50& Target | IC50: 10 nM (D1 dopamine receptor), D5 dopamine receptor, 660 nM (D2 dopamine receptor)[1] | ||||||||||||||||
体外研究 (In Vitro) | Dihydrexidine (DAR-0100) strongly increased YAP phosphorylation in U2OS cells[5]. | ||||||||||||||||
体内研究 (In Vivo) | Dihydrexidine hydrochloride has poor oral bioavailability and a relatively short half-life of 1 to 2 h[3].
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Clinical Trial | |||||||||||||||||
分子量 | 303.78 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H18ClNO2 | ||||||||||||||||
CAS 号 | 137417-08-4 | ||||||||||||||||
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 : 83.33 mg/mL(274.31 mM;Need ultrasonic) H2O : 10 mg/mL(32.92 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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