1. Academic Validation
  2. Inflammation Modulatory Phorbol Esters from the Seeds of Aquilaria malaccensis

Inflammation Modulatory Phorbol Esters from the Seeds of Aquilaria malaccensis

  • J Nat Prod. 2017 May 26;80(5):1421-1427. doi: 10.1021/acs.jnatprod.6b01096.
Vitthal D Wagh Michal Korinek I-Wen Lo Yu-Ming Hsu Shu-Li Chen Hsue-Yin Hsu 1 Tsong-Long Hwang 2 3 4 Yang-Chang Wu Bing-Hung Chen Yuan-Bin Cheng Fang-Rong Chang
Affiliations

Affiliations

  • 1 Department of Life Sciences, Tzu Chi University , Hualien 970, Taiwan.
  • 2 Graduate Institute of Natural Products, College of Medicine, and Chinese Herbal Medicine Research Team, Healthy Aging Research Center, Chang Gung University , Taoyuan 333, Taiwan.
  • 3 Research Center for Chinese Herbal Medicine, Research Center for Food and Cosmetic Safety, and Graduate Institute of Health Industry Technology, College of Human Ecology, Chang Gung University of Science and Technology , Taoyuan 333, Taiwan.
  • 4 Department of Anesthesiology, Chang Gung Memorial Hospital , Taoyuan 333, Taiwan.
Abstract

The tree Aquilaria malaccensis is a valuable source of agarwood, which is used in herbal medicinal preparations. Phytochemical research on A. malaccensis seeds has led to the isolation of four new phorbol esters (1-4), two known phorbol esters (5, isolated from Nature for the first time, and 6), and two known glycerides (7 and 8). The structures of these isolates were elucidated by means of spectroscopic data interpretation. The inflammation-modulatory activities of the isolates on Elastase release and superoxide anion generation in human neutrophils were evaluated. Interestingly, phorbol esters 1, 5, and 6 showed potent inhibitory activity on Elastase release in human neutrophils, with IC50 values of 2.7, 0.8, and 2.1 μM, respectively. All isolated phorbol esters exerted enhancing activity on superoxide anion generation. The results indicated that phorbol esters may play a bilateral modulatory role in the processes of inflammation. In addition, the compounds were evaluated for their cytotoxic properties against HepG2 (hepatoma), MDA-MB-231 (breast), and A549 (lung) Cancer cells, but all compounds were inactive for all cell lines used (IC50 > 10 μM).

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