期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 58, 期 10, 页码 4278-4290出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.5b00257
关键词
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An empirical approach to improve the microsomal stability and CYP inhibition profile of lead compounds 1a and 1b led to the identification of 5 (BMS-341) as a dissociated glucocorticoid receptor modulator. Compound 5 showed significant improvements in pharmacokinetic properties and, unlike compounds 1a-b, displayed a linear, dose-dependent pharmacokinetic profile in rats. When tested in a chronic model of adjuvant-induced arthritis in rat, the ED50 of 5 (0.9 mg/kg) was superior to that of both 1a and 1b (8 and 17 mg/kg, respectively).
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