期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 54, 期 17, 页码 6050-6062出版社
AMER CHEMICAL SOC
DOI: 10.1021/jm2005354
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Structure based design led directly to 1,3-oxazinan-2-one 9a with an IC50 of 42 nM against 11 beta-HSD1 in vitro. Optimization of 9a for improved in vitro enzymatic and cellular potency afforded 25f with IC50 values of 0.8 nM for the enzyme and 2.5 nM in adipocytes. In addition, 25f has 94% oral bioavailability in rat and >1000 x selectivity over 11 beta-HSD2. In mice, 251 was distributed to the target tissues, liver, and adipose, and in cynomolgus monkeys a 10 mg/kg oral dose reduced cortisol production by 85% following a cortisone challenge.
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