1198166-32-3Relevant academic research and scientific papers
Discovery of a 2-hydroxyacetophenone derivative as an outstanding linker to enhance potency and β-selectivity of liver X receptor agonist
Koura, Minoru,Yamaguchi, Yuki,Kurobuchi, Sayaka,Sumida, Hisashi,Watanabe, Yuichiro,Enomoto, Takashi,Matsuda, Takayuki,Okuda, Ayumu,Koshizawa, Tomoaki,Matsumoto, Yuki,Shibuya, Kimiyuki
supporting information, p. 3436 - 3446 (2016/07/21)
Our research found that the 2-hydroxyacetophenone derivative is an outstanding linker between the 1,1-bistrifluoromethylcarbinol moiety and the imidazolidine-2,4-dione moiety to enhance the potency and β-selectivity of liver X receptor (LXR) agonist in ou
CARBINOL DERIVATIVES HAVING CYCLIC LINKER
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Page/Page column 72, (2010/03/31)
[Object] To provide a novel LXRβ agonist that is useful as a preventative and/or therapeutic agent for atherosclerosis; arteriosclerosis such as those resulting from diabetes; dyslipidemia; hypercholesterolemia; lipid-related diseases; inflammatory diseases that are caused by inflammatory cytokines; skin diseases such as allergic skin diseases; diabetes; or Alzheimer's disease. [Solving Means] A carbinol compound represented by the following general formula (I) or salt thereof, or their solvate.
