CAS NO: | 42200-33-9 |
包装 | 价格(元) |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Nadolol (SQ-11725) is a non-selective and orally activeβ-adrenergic receptorsblocker and is a substrate of organic anion transporting polypeptide 1A2 (OATP1A2). Nadolol has the the potential for high blood pressure, angina pectoris and vascular headaches research[1][2][3]. | ||||||||||||||||
体外研究 (In Vitro) | In human embryonic kidney 293 cells, (-)-Epigallocatechin gallate (EGCG) competitively inhibits OATP1A2-mediated uptake of Nadolol with a Kivalue of 19.4 μM. With respect to Nadolol, the Kmfor OATP1A2 is 84 μM[2]. | ||||||||||||||||
体内研究 (In Vivo) | In male OF1 mice bearing B16F10 tumor cells, blocking the neuroendocrine response through the administration of Nadolol (20 mg/kg) results in fewer and smaller pulmonary metastatic foci in subjects exposed to acute social stress[3]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 309.40 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H27NO4 | ||||||||||||||||
CAS 号 | 42200-33-9 | ||||||||||||||||
中文名称 | 纳多洛尔 | ||||||||||||||||
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(161.60 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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