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Isoprenylated flavonoids from Morus nigra and their PPAR γ agonistic activities.
Xu, Liang-Jin; Yu, Mei-Hua; Huang, Chun-Yue; Niu, Li-Xin; Wang, Yi-Fan; Wu, Chun-Zhen; Yang, Pei-Ming; Hu, Xiao.
Afiliação
  • Xu LJ; Innovation Center of Chinese Medicine, China State Institute of Pharmaceutical Industry, Shanghai 201203, China.
  • Yu MH; Department of Pharmacognosy, School of Pharmacy, Fudan University, Shanghai 201203, China.
  • Huang CY; Innovation Center of Chinese Medicine, China State Institute of Pharmaceutical Industry, Shanghai 201203, China.
  • Niu LX; Innovation Center of Chinese Medicine, China State Institute of Pharmaceutical Industry, Shanghai 201203, China.
  • Wang YF; Innovation Center of Chinese Medicine, China State Institute of Pharmaceutical Industry, Shanghai 201203, China; Department of Pharmacognosy, School of Pharmacy, Fudan University, Shanghai 201203, China.
  • Wu CZ; Innovation Center of Chinese Medicine, China State Institute of Pharmaceutical Industry, Shanghai 201203, China.
  • Yang PM; Innovation Center of Chinese Medicine, China State Institute of Pharmaceutical Industry, Shanghai 201203, China.
  • Hu X; Innovation Center of Chinese Medicine, China State Institute of Pharmaceutical Industry, Shanghai 201203, China. Electronic address: xjtuyxhx@126.com.
Fitoterapia ; 127: 109-114, 2018 Jun.
Article em En | MEDLINE | ID: mdl-29427594
ABSTRACT
A novel dihydroflavonol unprecedentedly with a prenyl group at C-2, nigragenon A (1), four new sanggenon-type flavonones, nigragenons B-E (2-5), along with six known isoprenylated flavonoids (6-11) were isolated from the twigs of Morus nigra. Their structures were elucidated through extensive analysis of spectroscopic data. Interestingly, compound 1 was the first reported biogenetic precursor of sanggenon-type flavanones and the biogenetic pathway from 1 to sanggenol F was proposed. The PPAR γ agonistic activity was investigated in HEK293 cells using dual luciferase reporter assay. Compounds 2, 4, 7, and 9 showed obvious agonistic activities on PPAR γ, and compound 2 was a potential PPAR γ partial agonist. Moreover, the preliminary structure-activity relationships for the tested compounds were discussed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Flavonoides / Morus / PPAR gama Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Flavonoides / Morus / PPAR gama Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article