维生素D3衍生物的侧链化工程用于VDR静音SREBP抑制剂

Fumihiro Kawagoe1, Sayuri Mototani1, Tomofumi Yatsu1

  • 1Faculty of Pharmaceutical Sciences, Teikyo University, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.

PubMed
概括

研究人员开发了新的化维生素D3类似物,其目标是抑制固醇调节元素结合蛋白 (SREBP). 化合物11通过最小的维生素D受体 (VDR) 激活选择性抑制SREBP,提供了一个有前途的治疗途径.

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