13,14-seco seco withaphysalins from Physalis minima and their inhibitory effects on NLRP3 inflammasome activation
文献类型:期刊论文
作者 | Hu, Bintao6,7; Peng, Xia5; Tang, Chunping6,7![]() ![]() ![]() ![]() ![]() |
刊名 | BIOORGANIC CHEMISTRY
![]() |
出版日期 | 2024-10-01 |
卷号 | 151页码:12 |
关键词 | Physalis minima NLRP3 Anti-inflammatory 13,14-seco withaphysalin |
ISSN号 | 0045-2068 |
DOI | 10.1016/j.bioorg.2024.107630 |
通讯作者 | Yao, Sheng(yaosheng@simm.ac.cn) ; Ai, Jing(jai@simm.ac.cn) ; Ye, Yang(yye@simm.ac.cn) |
英文摘要 | Seven new 13,14-seco withaphysalins including two new skeletons (1 and 9) were isolated from the whole plants of Physalis minima, together with three known analogues (6-8). Among them, compound 1 was an extremely rare steroid with a 6, 8-cyclo ring. Their structures were established by extensive analysis of spectroscopic data, experimental electronic circular dichroism measurements, and single-crystal X-ray crystallographic analysis. In Raw264.7 cells, compounds 1-3, 5, 6, and 8 demonstrated potent ability to reduce the NLRP3-dependent caspase-1 activation. Among these compounds, 1 and 2 showed a superior potential, consistently concentrationdependent downregulating NLRP3-dependent proinflammatory cytokine IL-1/i production in macrophage. Mechanistically, compounds 1 and 2 reduced the cleavage of caspase-1 and GSDMD, and exhibited no obvious impact both on the NF-kappa B activation and the expression of NLRP3 and IL-1/i, suggesting that the compounds target the activation of the NLRP3 pathway mainly by inhibiting the NLRP3 inflammasome activation step rather than the priming step. |
WOS关键词 | WITHANOLIDES ; MECHANISM |
资助项目 | Natural Science Foundation of China for Innovation Research Group[81821005] ; National Key R & D Program of China[2017YFE0195100] ; National Key R & D Program of China[2022YFE0203600] ; National Natural Science Foundation of China[81903485] ; Science and Technology Commission of Shanghai Municipality[19431908100] ; Collaborative Innovation Cluster Project of Shanghai Municipal Commission of Health and Family Planning[2020CXJQ02] ; Key-Area Research and Development Program of Guangdong Province[2020B0303070002] ; High-level new R D institute[2019B090904008] ; High-level Innovative Research Institute from Department of Science and Technology of Guangdong Province[2021B0909050003] ; Department of Science and Technology of Guangdong Province ; Project of Shanghai Institute of Materia Medica, Chinese Academy of Sciences[SIMM0120231001] |
WOS研究方向 | Biochemistry & Molecular Biology ; Chemistry |
语种 | 英语 |
WOS记录号 | WOS:001281418700001 |
出版者 | ACADEMIC PRESS INC ELSEVIER SCIENCE |
源URL | [http://119.78.100.183/handle/2S10ELR8/312583] ![]() |
专题 | 新药研究国家重点实验室 |
通讯作者 | Yao, Sheng; Ai, Jing; Ye, Yang |
作者单位 | 1.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201203, Peoples R China 2.Chinese Acad Sci, Shanghai Inst Mat Med, Zhongshan Inst Drug Discovery, Zhongshan 528400, Peoples R China 3.Bohai Rim Adv Res Inst Drug Discovery, Shandong Lab Yantai Drug Discovery, Yantai 264117, Shandong, Peoples R China 4.Univ Chinese Acad Sci, Beijing 100049, Peoples R China 5.Nanjing Univ Chinese Med, Sch Chinese Mat Med, Nanjing 210023, Peoples R China 6.Chinese Acad Sci, Shanghai Inst Mat Med, Nat Prod Chem Dept, Shanghai 201203, Peoples R China 7.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China |
推荐引用方式 GB/T 7714 | Hu, Bintao,Peng, Xia,Tang, Chunping,et al. 13,14-seco seco withaphysalins from Physalis minima and their inhibitory effects on NLRP3 inflammasome activation[J]. BIOORGANIC CHEMISTRY,2024,151:12. |
APA | Hu, Bintao.,Peng, Xia.,Tang, Chunping.,Geng, Meiyu.,Yao, Sheng.,...&Ye, Yang.(2024).13,14-seco seco withaphysalins from Physalis minima and their inhibitory effects on NLRP3 inflammasome activation.BIOORGANIC CHEMISTRY,151,12. |
MLA | Hu, Bintao,et al."13,14-seco seco withaphysalins from Physalis minima and their inhibitory effects on NLRP3 inflammasome activation".BIOORGANIC CHEMISTRY 151(2024):12. |
入库方式: OAI收割
来源:上海药物研究所
浏览0
下载0
收藏0
其他版本
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。