Discovery of PPARγ and glucocorticoid receptor dual agonists to promote the adiponectin and leptin biosynthesis in human bone marrow mesenchymal stem cells
作者:Sungjin Ahn、Myunghwan Ahn、Suzie Park、Seungchan An、In Guk Park、Seok Young Hwang、Junpyo Gong、Soyeon Oh、Sun Hee Jin、Hee Jin Kim、Jae Hoon Cheong、Youngjoo Byun、Minsoo Noh
DOI:10.1016/j.ejmech.2022.114927
日期:2023.1
Using the compound 1 structure, the structure-activity relationship study was performed to discover more potent compounds stimulating both adiponectin and leptin production. (E)-3-(3-(2-fluoropyridin-4-yl)acryloyl)-4-hydroxy-6-methyl-2H-pyran-2-one (11) exhibited the most potent adiponectin (EC50, 2.87 μM) and leptin (EC50, 2.82 μM) biosynthesis-stimulating activities in hBM-MSCs. In a target identification
脂联素和瘦素是控制脂肪组织和其他器官系统之间串扰的主要脂肪细胞因子。低脂联素血症和低瘦素血症与人类代谢疾病有关。具有脂肪细胞因子生物合成刺激活性的化合物可以开发为针对不同代谢条件的治疗剂。在人骨髓间充质干细胞 (hBM-MSCs) 的表型筛选中,( E )-4-hydroxy-3-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)-6-methyl-2 H -pyran- 2-one ( 1 ) 被鉴定为在脂肪形成过程中增加脂联素生物合成,同时刺激瘦素的产生。使用化合物1结构,进行构效关系研究以发现更有效的化合物刺激脂联素和瘦素的产生。( E )-3-(3-(2-fluoropyridin-4-yl)acryloyl)-4-hydroxy-6-methyl-2 H -pyran-2-one ( 11 ) 表现出最有效的脂联素 (EC 50 , 2.87 μM) 和瘦素