Design and discovery of 2-oxochromene derivatives as liver X receptor β-selective agonists
作者:Takayuki Matsuda、Ayumu Okuda、Yuichiro Watanabe、Tohru Miura、Hidefumi Ozawa、Ayako Tosaka、Koichi Yamazaki、Yuki Yamaguchi、Sayaka Kurobuchi、Minoru Koura、Kimiyuki Shibuya
DOI:10.1016/j.bmcl.2015.01.047
日期:2015.3
an attempt to molecularly design liver X receptor (LXR) β-selective agonists, we discovered that the combination of the 2-oxochromene moiety (head) and the imidazoline-2,4-dione moiety (tail) plays an important role in the expression potency and selectivity toward LXRβ. We synthesized a series of 2-oxochromene derivatives and identified 43 as a LXRβ-selective agonist that increased the HDL-C level without
在分子设计肝X受体(LXR)β-选择性激动剂的尝试中,我们发现2-氧代色烯部分(头部)和咪唑啉-2,4-二酮部分(尾巴)的组合在表达能力和对LXRβ的选择性。我们合成了一系列2-oxochromene衍生物,并确定了43种LXRβ选择性激动剂,可在不显着升高TG水平的情况下增加HDL-C水平,并导致高脂饮食中主动脉弓内脂质蓄积面积减少。和胆固醇喂养的Bio F 1 B仓鼠。在这份手稿中,我们报告了这些2-氧代苯并二氢吡喃衍生物的设计,合成和药理作用。