AdipoRon是AdipoR激动剂,能与AdipoR1和AdipoR2结合,Kd分别为1.8 uM和3.1 uM。
AdipoRon is a novel, and orally bioavailable adiponectin receptor agonist with KD of 1.8 and 3.1 μM for AdipoR1 and AdipoR2, respectively.
~50mg/kgi.v.或 p.o.
动物 A (mg/kg) = 动物 B (mg/kg)×动物 B的Km系数/动物 A的Km系数 | |
例如,已知某工具药用于小鼠的剂量为88 mg/kg , 则用于大鼠的剂量换算方法:将88 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到该药物用于大鼠的等效剂量44 mg/kg。
[1] Okada-Iwabu M, et al. Nature. 2013, 503(7477), 493-499.
[2] Yanqing Zhang,et al. AdipoRon, the first orally active adiponectin receptor activator, attenuates postischemic myocardial apoptosis through both AMPK-mediated and AMPK-independent signalings. Am J Physiol Endocrinol Metab. 2015 Aug 1; 309(3): E275–E282. Published online 2015 Jun 2. doi: 10.1152/ajpendo.00577.2014.
[3] William L. et al. Ronning After the Adiponectin Receptors. Science. Author manuscript; available in PMC 2014 Dec 20. Published in final edited form as: Science. 2013 Dec 20; 342(6165): 1460–1461. doi: 10.1126/science.1249077.
分子式 C27H28N2O3 |
分子量 428.52 |
CAS号 924416-43-3 |
储存方式 ﹣20 ℃冷藏长期储存。冰袋运输 |
溶剂(常温) |
DMSO 86 mg/mL |
Water Insoluble |
Ethanol 50 mg/mL |
体内溶解度
NCT03032991 | Gestational Diabetes Mellitus in Childbirth|Neurodevelopmental Disorders | Universidad de Murcia|Universidad de Granada | 2016-01-01 | 2017-01-23 |
注:以上所有数据均来自公开文献,并不保证对所有实验均有效,数据仅供参考。
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