Naphthofuranone derivatives and other constituents from Pachira aquatica with inhibitory activity on superoxide anion generation by neutrophils
- Fitoterapia. 2017 Mar:117:16-21. doi: 10.1016/j.fitote.2016.12.008.
- 1. School of Pharmacy, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
- 2. Graduate Institute of Natural Products, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan.
- 3. Department of Pharmacy, Tajen University, Pingtung 90741, Taiwan; Department of Pharmacy, Zuoying Branch of Kaohsiung Armed Forces General Hospital, Kaohsiung 81342, Taiwan.
- 4. Department of Medicine, Mackay Medical College, New Taipei City 25245, Taiwan.
- 5. Department of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, China Medical University, Taichung 40402, Taiwan; Department of Biotechnology, Asia University, Taichung 41354, Taiwan.
- 6. Department of Pharmacy, Tajen University, Pingtung 90741, Taiwan; Department of Medical Research, China Medical University Hospital, China Medical University, Taichung 40447, Taiwan. Electronic address: [email protected].
Two new naphthofuranone derivatives, 11-hydroxy-2-O-methylhibiscolactone A (1) and O-methylhibiscone D (2), have been isolated from the stems of Pachira aquatica, together with 18 known compounds (3-20). The structures of two new compounds were determined through spectroscopic and MS analyses. Among the isolated compounds, 11-hydroxy-2-O-methylhibiscolactone A (1), isohemigossylic acid lactone-7-methyl ether (4), gmelofuran (6), and 5-hydroxyauranetin (8) exhibited inhibition (IC50≤28.84μM) of superoxide anion generation by human neutrophils in response to N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLP).
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Cat. No.Product NameDescriptionTargetResearch Area
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target: OthersResearch Areas: Inflammation/Immunology