Dysiarenone, a Dimeric C21 Meroterpenoid with Inhibition of COX-2 Expression from the Marine Sponge Dysidea arenaria

被引:36
作者
Jiao, Wei-Hua [1 ]
Cheng, Bao-Hui [2 ,3 ]
Chen, Guo-Dong [4 ]
Shi, Guo-Hua [1 ]
Li, Jing [1 ]
Hu, Tian-Yong [2 ,3 ]
Lin, Hou-Wen [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, Dept Pharm,Res Ctr Marine Drugs,State Key Lab Onc, Shanghai 200127, Peoples R China
[2] Longgang ENT Hosp, Shenzhen Key Lab ENT, Shenzhen 518172, Peoples R China
[3] Inst ENT, Shenzhen 518172, Peoples R China
[4] Jinan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
SESQUITERPENE QUINONES; NATURAL-PRODUCTS; A-C; AMINOQUINONES; PUUPEHENONE; AVARA;
D O I
10.1021/acs.orglett.8b01148
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Dysiarenone (1), a dimeric C-21 meroterpenoid featuring an unprecedented 2-oxaspiro[bicyclo[3.3.1]nonane-9,1'-cyclopentane] carbon skeleton, was isolated from the marine sponge Dysidea arenaria. The structure of 1 was determined by HRMS and NMR spectroscopic analyses coupled with ECD calculations. Dysiarenone showed inhibitory activities against COX-2 expression and the production of prostaglandin E-2 with an IC50 value of 6.4 mu M in LPS-stimulated RAW264.7 macrophages.
引用
收藏
页码:3092 / 3095
页数:4
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