Planta Med 2018; 84(18): 1340-1347
DOI: 10.1055/a-0645-1437
Natural Product Chemistry and Analytical Studies
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Four New 2-(2-Phenylethyl)-4H-chromen-4-one Derivatives from the Resinous Wood of Aquilaria sinensis and Their Inhibitory Activities on Neutrophil Pro-Inflammatory Responses

Authors

  • Sin-Ling Wang

    1   School of Pharmacy, College of Pharmacy, Kaohsiung Medical University, Kaohsiung, Taiwan
  • Hsiang-Ruei Liao

    2   Graduate Institute of Natural Products, College of Medicine, Chang Gung University, Taoyuan, Taiwan
  • Ming-Jen Cheng

    3   Bioresource Collection and Research Center (BCRC), Food Industry Research and Development Institute (FIRDI), Hsinchu, Taiwan
  • Chih-Wen Shu

    4   Department of Medical Education and Research, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan
  • Chun-Lin Chen

    5   Department of Biological Sciences, National Sun Yat-Sen University, Kaohsiung, Taiwan
  • Mei-Ing Chung

    1   School of Pharmacy, College of Pharmacy, Kaohsiung Medical University, Kaohsiung, Taiwan
  • Jih-Jung Chen

    6   Faculty of Pharmacy, School of Pharmaceutical Sciences, National Yang-Ming University, Taipei, Taiwan
    7   Department of Medical Research, China Medical University Hospital, China Medical University, Taichung, Taiwan
Further Information

Publication History

received 16 February 2018
revised 31 May 2018

accepted 14 June 2018

Publication Date:
28 June 2018 (online)

Preview

Abstract

Four new 2-(2-phenylethyl)-4H-chromen-4-one derivatives, 6-hydroxy-5-methoxy-2-[2-(4′-methoxyphenyl)ethyl]chromone (1), 6,7-dimethoxy-2-[2-(2′-hydroxyphenyl)ethyl]chromone (2), 5-hydroxy-6-methoxy-2-[2-(3′-methoxyphenyl)ethyl]-chromone (3), and 7-chloro-8-hydroxy-2-[2-(4′-methoxyphenyl)ethyl]chromone (4), have been isolated from the resinous wood of Aquilaria sinensis, together with 16 known compounds (520). Among these, 7-methoxy-2-[2-(4′-methoxyphenyl)ethyl]chromone (5) was isolated from a natural source for the first time. The structures of the new compounds were established by spectroscopic analyses (1D and 2D NMR, HR-ESI-MS, IR, UV). Nine compounds, including 1 showed more than 80% inhibition of superoxide anion generation by human neutrophils in response to formyl-L-methionyl-L-leucyl-L-phenylalanine at 50 µM.

Supporting Information