Three New Clerodane Diterpenoids and Their NLRP3 Inflammasome Activation Inhibitory Activity from Callicarpa arborea Roxb

被引:0
|
作者
Zeb, Muhammad Aurang [1 ,2 ]
Ding, Ling [1 ,2 ]
Wang, Meng-Ru [1 ,2 ]
Tu, Wen-Chao [1 ,2 ]
Li, Xiao-Li [1 ,2 ]
Zhang, Xing-Jie [1 ,2 ]
Xiao, Wei-Lie [1 ,2 ]
机构
[1] Yunnan Univ, Sch Chem Sci & Technol, Yunnan Res & Dev Ctr Nat Prod, Minist Educ,Yunnan Characterist Plant Extract Lab,, Kunming 650500, Peoples R China
[2] Yunnan Univ, Sch Pharm, State Key Lab Conservat & Utilizat Bioresources Yu, Kunming 650500, Peoples R China
基金
中国国家自然科学基金;
关键词
Callicarpa; clerodane diterpenoids; NLRP3; inflammasome; spectroscopy; DP4+; CELLS;
D O I
10.1002/cbdv.202301676
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Three new compounds callicarpenoids A-C (1-3), were isolated from the stems of Callicarpa arborea Roxb together with fifteen known compounds (4-18). The structures of these compounds were elucidated using advanced spectroscopic techniques, including 1D and 2D NMR, UV, IR, HR-ESI-MS, ECD, ORD, and quantum chemical calculations. Compound 3, a rare rearranged diterpenoid with a fused 5/6-ring system demonstrated strong potential as an inhibitor of the NLRP3 inflammasome activation with an IC50 value of 3.153 mu M. It effectively reduced GSDMD-NT production, inhibited caspase-1 activation, and suppressed IL-1 beta secretion, thereby mitigating NLRP3 inflammasome-induced pyroptosis in J774A.1 cells. These findings suggest that compound 3 warrants further research and development as a promising NLRP3 inflammasome inhibitor.
引用
收藏
页数:10
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