CAS NO: | 1024033-43-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | AZD 4017 is a potent, selective 11β-Hydroxysteroid Dehydrogenase Type 1(11β-HSD1)inhibitor, with anIC50of 7 nM. | ||||||||||||||||
IC50& Target | IC50: 7 nM (11β-HSD1)[1]. | ||||||||||||||||
体外研究 (In Vitro) | AZD 4017 displays excellent selectivity versus the related enzymes 11-βHSD2, 17β-HSD1, 17β-HSD3 (all IC50>30 μM) and shows no measurable activity against the glucocorticoid and mineralocorticoid receptors. Despite having high potency for the human form of 11β-HSD1, AZD 4017 shows much reduced activity across species with the exception of cynomolgous monkey (IC50=0.029 μM). Additionally, as it is believed that adipose is a key target organ, inhibition of 11β-HSD1 activity is measured in isolated human adipocytes from nondiabetic volunteers. AZD 4017 is shown to be a potent inhibitor in this key target tissue (IC50=0.002 μM) in good agreement with the enzyme potency, thus providing some confidence that AZD 4017 is not restricted from adipose tissue by the fact that it was acidic[1]. | ||||||||||||||||
体内研究 (In Vivo) | Since AZD 4017 has lower potency against the mouse enzyme, only a limited number of preclinical pharmacodynamic measurements are performed. Increasing the dose further led to a maximal effect of approximately 70% inhibition at 1500 mg/kg, equivalent to 10×IC50in the mouse, demonstrating the dose dependent inhibition of 11β-HSD1 by AZD 4017 in this model[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 419.58 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C22H33N3O3S | ||||||||||||||||
CAS 号 | 1024033-43-9 | ||||||||||||||||
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 : 125 mg/mL(297.92 mM;Need ultrasonic) 配制储备液
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