Phenolic Constituents Isolated from the Twigs of Cinnamomum cassia and Their Potential Neuroprotective Effects

  • J Nat Prod. 2018 Jun 22;81(6):1333-1342. doi: 10.1021/acs.jnatprod.7b00924.
Xin Liu  1 Jing Fu  1 Xiao-Jun Yao  1 Ji Yang  1 Liang Liu  1 Tang-Gui Xie  2 Ping-Chuan Jiang  2 Zhi-Hong Jiang  1  3 Guo-Yuan Zhu  1
Affiliations
  • 1. State Key Laboratory of Quality Research in Chinese Medicine, Macau Institute for Applied Research in Medicine and Health , Macau University of Science and Technology , Macau , People's Republic of China.
  • 2. Guangxi Key Laboratory of Traditional Chinese Medicine Quality Standards , Guangxi Institute of Chinese Medicine and Pharmaceutical Science , Nanning 530022 , People's Republic of China.
  • 3. International Institute for Translational Chinese Medicine , Guangzhou University of Chinese Medicine , Guangzhou 510006 , People's Republic of China.
Abstract

Seven new α,β-diphenyl-γ-butyrolactones (1-7), three new Lignans (8-10), five new neolignans (11-15), two new 1,3-biphenylpropanoids (16 and 17), and a new flavonol galactoside-lignan ester (18), together with 43 known compounds (19-61), were isolated from the twigs of Cinnamomum Cassia. Their structures were elucidated by spectroscopic data analysis as well as chemical methods. The α,β-diphenyl-γ-butyrolactones are a class of unique natural compounds that have only been isolated from C. Cassia. Compounds 11 and 12 are rare examples of neolignans possessing a 1,2-dioxetane moiety. Compound 13 is a new oxyneolignan possessing a unique C-9-O-C-9' linkage between the benzopyran and cinnamyl alcohol moieties. Compound 15 is the first example of a natural neolignan possessing a 2-styryl-3-phenyltetrahydrofuran skeleton. The isolated compounds were evaluated for their neuroprotective activities against tunicamycin-induced cytotoxicity in SH-SY5Y cells. Compounds 3, 5, 10, 11, 12, 20, 36, and 56 showed statistically significant neuroprotective activity with EC50 values ranging between 21 and 75 μM.