Vitamin D(3) metabolites block lipid biosynthesis by promoting degradation of the complex of sterol regulatory element-binding protein (SREBP) and SREBP cleavage-activating protein (SCAP) independent of their effects on the vitamin D receptor (VDR). We previously reported the development of KK-052, the first vitamin D-based SREBP inhibitor that mitigates hepatic lipid accumulation without VDR-mediated calcemic action in mice. Herein we extend our previous work to synthesize KK-052 analogues. Various substituents were introduced to the phenyl ring of KK-052, and two KK-052 analogues were found to exhibit more potent SREBP/SCAP inhibitory activity than KK-052, whereas they all lack VDR activity. These new KK-052 analogues may be suited for further development as VDR-silent SREBP/SCAP inhibitors.
Structure-activity relationship studies on vitamin D-based selective SREBP/SCAP inhibitor KK-052.
基于维生素 D 的选择性 SREBP/SCAP 抑制剂 KK-052 的构效关系研究
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作者:Kawagoe Fumihiro, Mototani Sayuri, Mendoza Aileen, Takemoto Yasushi, Uesugi Motonari, Kittaka Atsushi
| 期刊: | RSC Medicinal Chemistry | 影响因子: | 3.600 |
| 时间: | 2023 | 起止号: | 2023 Aug 15; 14(10):2030-2034 |
| doi: | 10.1039/d3md00352c | 研究方向: | 信号转导 |
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