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新型布查丁衍生物作为潜在的抗肥胖治疗脂肪生成/脂质生成抑制剂的合成与生物学评价

Synthesis and Biological Evaluation of Novel Bouchardatine Derivatives as Potential Adipogenesis/Lipogenesis Inhibitors for Antiobesity Treatment.

作者信息

Rao Yong, Liu Hong, Gao Lin, Yu Hong, Ou Tian-Miao, Tan Jia-Heng, Huang Shi-Liang, Wang Hong-Gen, Li Ding, Gu Lian-Quan, Ye Ji-Ming, Huang Zhi-Shu

机构信息

School of Pharmaceutical Sciences, Sun Yat-Sen University , Guangzhou 510006, People's Republic of China.

Molecular Pharmacology for Diabetes Group, Health Innovations Research Institute and School of Health Sciences, RMIT University , Melbourne, Victoria 3083, Australia.

出版信息

J Med Chem. 2015 Dec 10;58(23):9395-413. doi: 10.1021/acs.jmedchem.5b01566. Epub 2015 Dec 1.

Abstract

Our recent study has shown that the natural product bouchardatine (1) can reduce the triglyceride (TG) content in 3T3-L1 adipocytes (EC50 ≈ 25 μM). Here, we synthesized two series of compounds by introducing amine side chains at the 5 or 8 position of 1 and evaluated the lipid-lowering activity of derivatives. It was found that some of the compounds had significant lipid-lowering effects, and the most active compound 3d showed better activity (EC50 = 0.017 μM) than 2 (EC50 = 0.086 μM), a compound reported by us. Further, the mechanism studies revealed that 3d blocked TG accumulation via activation of the LKB1-AMPK signaling pathway, efficiently down-regulating the expression of key regulators of adipogenesis/lipogenesis. Cell uptake assay and confocal imaging of 3d in cells indicated that compound 3d had favorable cell permeability. Our results suggest that 3d may be a promising agent for the treatment of obesity and related metabolic disorders.

摘要

我们最近的研究表明,天然产物布查丁(1)可降低3T3-L1脂肪细胞中的甘油三酯(TG)含量(半数有效浓度约为25 μM)。在此,我们通过在1的5位或8位引入胺侧链合成了两个系列的化合物,并评估了衍生物的降脂活性。结果发现,其中一些化合物具有显著的降脂作用,活性最强的化合物3d表现出比我们报道的化合物2(半数有效浓度 = 0.086 μM)更好的活性(半数有效浓度 = 0.017 μM)。此外,机制研究表明,3d通过激活LKB1-AMPK信号通路阻断TG积累,有效下调脂肪生成/脂质生成关键调节因子的表达。细胞摄取实验和3d在细胞中的共聚焦成像表明,化合物3d具有良好的细胞通透性。我们的结果表明,3d可能是治疗肥胖症及相关代谢紊乱的一种有前景的药物。

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