1. Academic Validation
  2. Phenolic Constituents Isolated from the Twigs of Cinnamomum cassia and Their Potential Neuroprotective Effects

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

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.

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