Your browser doesn't support javascript.
loading
Diterpenoids from aerial parts of Flickingeria fimbriata and their nuclear factor-kappaB inhibitory activities.
Li, Hang; Zhao, Jing-Jun; Chen, Jin-Long; Zhu, Long-Ping; Wang, Dong-Mei; Jiang, Lin; Yang, De-Po; Zhao, Zhi-Min.
Afiliación
  • Li H; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China.
  • Zhao JJ; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China.
  • Chen JL; School of Environmental and Chemical Engineering, Nanchang University, Nanchang, Jiangxi 330031, China.
  • Zhu LP; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China; Guangdong Technology Research Center for Advanced Chinese Medicine, Guangzhou, Guangdong 510006, China.
  • Wang DM; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China; Guangdong Technology Research Center for Advanced Chinese Medicine, Guangzhou, Guangdong 510006, China.
  • Jiang L; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China; Guangdong Technology Research Center for Advanced Chinese Medicine, Guangzhou, Guangdong 510006, China.
  • Yang DP; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China; Guangdong Technology Research Center for Advanced Chinese Medicine, Guangzhou, Guangdong 510006, China. Electronic address: lssydp@mail.sysu.edu.cn.
  • Zhao ZM; School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China; Guangdong Technology Research Center for Advanced Chinese Medicine, Guangzhou, Guangdong 510006, China. Electronic address: zhaozhm2@mail.sysu.edu.cn.
Phytochemistry ; 117: 400-409, 2015 Sep.
Article en En | MEDLINE | ID: mdl-26186245
ABSTRACT
Chemical investigation of the aerial parts of Flickingeria fimbriata (Bl.) Hawkes resulted in isolation of sixteen ent-pimarane diterpenoids, including five rare 16-nor-ent-pimarane diterpenoids, two 15,16-dinor-ent-pimarane diterpenoids and one ent-pimarane diterpenoid. Structures were mainly elucidated by extensive spectroscopic analysis, and their absolute configurations were unequivocally determined by the exciton chirality method, the modified Mosher's method, the CD experiments (including Snatzke's method) and chemical transformations, respectively. All the isolated compounds were screened for inhibitory effects on the nuclear factor-kappaB (NF-κB) in lipopolysaccharide (LPS) induced murine macrophage RAW264.7 cells, using a NF-κB-dependent luciferase reporter gene assay. Several of these compounds displayed comparable or even better activities than the positive control pyrrolidinedithiocarbamate (PDTC) (IC50=26.3 µM) with IC50 values in the range of 14.7-29.2 µM and structure-activity relationships are briefly proposed.
Asunto(s)
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: FN-kappa B / Orchidaceae / Diterpenos Idioma: En Revista: Phytochemistry Año: 2015 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: FN-kappa B / Orchidaceae / Diterpenos Idioma: En Revista: Phytochemistry Año: 2015 Tipo del documento: Article País de afiliación: China