Kainuma Masahiko, Kasuga Jun-ichi, Hosoda Shinnosuke, Wakabayashi Ken-ichi, Tanatani Aya, Nagasawa Kazuo, Miyachi Hiroyuki, Makishima Makoto, Hashimoto Yuichi
Institute of Molecular and Cellular Biosciences, University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.
Bioorg Med Chem Lett. 2006 Jun 15;16(12):3213-8. doi: 10.1016/j.bmcl.2006.03.075. Epub 2006 Apr 17.
Novel, potent farnesoid X receptor (FXR) and peroxisome proliferator-activated receptor alpha (PPARalpha) agonists were obtained by using a diphenylmethane skeleton as a substitute for a steroid skeleton.
通过使用二苯甲烷骨架替代甾体骨架,获得了新型强效法尼醇X受体(FXR)和过氧化物酶体增殖物激活受体α(PPARα)激动剂。