Chemical structures of constituents from the flowers of Osmanthus fragrans var. aurantiacus

被引:0
作者
Jiang Liu
Seikou Nakamura
Bin Xu
Takahiro Matsumoto
Tomoe Ohta
Katsuyoshi Fujimoto
Keiko Ogawa
Masashi Fukaya
Shiori Miyake
Masayuki Yoshikawa
Hisashi Matsuda
机构
[1] Kyoto Pharmaceutical University,Department of Pharmacognosy
[2] Ministry of Agriculture,Key Laboratory of Crop Ecophysiology and Farming System in Southwest China
[3] Sichuan Agricultural University,undefined
来源
Journal of Natural Medicines | 2015年 / 69卷
关键词
var. ; Floraosmanoside; Floraosmanolactone; Megastigmane; -Decalactone; Medicinal flower;
D O I
暂无
中图分类号
学科分类号
摘要
Three new megastigmane glycosides named floraosmanosides I–III and a new γ-decalactone named floraosmanolactone I together with 16 known constituents were isolated from the flowers of Osmanthus fragrans var. aurantiacus cultivated in Guangxi Zhuang Autonomous Region, China. The chemical structures of the new compounds were elucidated on the basis of chemical and physicochemical evidence. Among them, ligustroside and (+)-pinoresinol significantly inhibited nitric oxide production in lipopolysaccharide-activated RAW264.7 macrophages.
引用
收藏
页码:135 / 141
页数:6
相关论文
共 220 条
[1]  
Yoo KH(2013)Pomolic acid induces apoptosis in SK-OV-3 human ovarian adenocarcinoma cells through the mitochondrial-mediated intrinsic and death receptor-induced extrinsic pathways Oncol Lett 5 386-390
[2]  
Park J-H(2011)Lignans from the flowers of Arch Pharm Res 34 2029-2035
[3]  
Lee DK(2011) var. J Korean Soc Appl Bi 54 206-210
[4]  
Fu YY(2010) and their inhibition effect on NO production J Korean Soc Appl Bi 53 371-374
[5]  
Baek NI(2014)24-ethylcholesta-4,24(28)-dien-3,6-dione from J Nat Med 68 1-8
[6]  
Chung IS(2014) var. J Nat Med 68 481-487
[7]  
Lee DG(2014) flowers inhibits the growth of human colon cancer cell line, HCT-116 Org Lett 16 3076-3078
[8]  
Lee SM(2014)Secoiridoid glycoside from the flowers of J Nat Prod 77 990-999
[9]  
Bang MH(2013) var. Phytochemistry 92 128-136
[10]  
Park H-J(2013) makino inhibited the activity of Tetrahedron Lett 54 32-34