Dysambiol, an Anti-inflammatory Secomeroterpenoid from a Dysidea sp. Marine Sponge

被引:0
|
作者
Jiao, Wei-Hua [1 ]
Li, Jia-Xin [1 ]
Liu, Hong-Yan [1 ,2 ]
Luo, Xiang-Chao [1 ]
Hu, Tian-Yong [3 ,4 ]
Shi, Guo-Hua [1 ]
Xie, Dong-Dong [1 ]
Chen, Hai-Feng [2 ]
Cheng, Bao-Hui [3 ,4 ]
Lin, Hou-Wen [1 ]
机构
[1] Shanghai Jiao Tong Univ, Ren Ji Hosp, Res Ctr Marine Drugs, Sch Med,State Key Lab Microbial Metabolism,Dept Ph, Shanghai 200127, Peoples R China
[2] Xiamen Univ, Sch Pharmaceut Sci, Xiamen 361102, Peoples R China
[3] Longgang ENT Hosp, Dept Otolaryngol, Shenzhen 518172, Peoples R China
[4] Inst ENT, Shenzhen Key Lab ENT, Shenzhen 518172, Peoples R China
基金
中国国家自然科学基金;
关键词
SESQUITERPENE-QUINONES; A-C; MEROTERPENOIDS; MACROLIDE;
D O I
10.1021/acs.orglett.3c02409
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An unusual secomeroterpenoid, dysambiol (1), was isolated from a Dysidea sp. marine sponge collected from the South China Sea. Dysambiol features an unprecedented secomeroterpene scaffold with a rare lactone bridge. The structure of 1 was determined by extensive spectroscopic analysis, Mosher's method, and electronic circular dichroism calculation. Dysambiol displayed potent anti-inflammatory activity in LPS-induced Raw 264.7 macrophages by regulating the NF-?B/MPAK signaling pathway.
引用
收藏
页码:6391 / 6395
页数:5
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