515138-44-0Relevant academic research and scientific papers
Synthesis of a novel human PPARδ selective agonist and its stimulatory effect on oligodendrocyte differentiation
Sakuma, Shogo,Endo, Tsuyoshi,Kanda, Takashi,Nakamura, Hideki,Yamasaki, Satomi,Yamakawa, Tomio
scheme or table, p. 240 - 244 (2011/02/27)
We successfully synthesized a novel peroxisome proliferator-activated receptor (PPAR)δ selective agonist, namely, compound 20, with a characteristic benzisoxazole ring. Compound 20 exhibited potent human PPARδ transactivation activity and high δ selectivity. Further, it stimulated differentiation of primary oligodendrocyte precursor cells in vitro, indicating that it may be an effective drug in the treatment of demyelinating disorders such as multiple sclerosis.
Biological evaluation of novel benzisoxazole derivatives as PPARδ agonists
Sakuma, Shogo,Endo, Tsuyoshi,Kanda, Takashi,Nakamura, Hideki,Yamasaki, Satomi,Yamakawa, Tomio
experimental part, p. 3255 - 3264 (2011/06/27)
We discovered novel peroxisome proliferator-activated receptor δ agonists with a characteristic benzisoxazole ring. Compound 5 exhibited potent human PPARδ transactivation activity. Furthermore, it stimulated the differentiation of oligodendrocyte precurs
ACTIVATOR FOR PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR DELTA
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Page 41, (2008/06/13)
A compound represented by the formula (I) or a salt of the compound, and a PPAR-δ activator which contains the compound or salt as the active ingredient: ???(wherein A represents O or S; B1 represents N, etc.; B2 represents O, etc.;
