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Undescribed Phenolic Glycosides from Syzygium attopeuense and Their Inhibition of Nitric Oxide Production
Authors:Prof. Phan Van Kiem  Dr. Bui Hai Ninh  Bui Huu Tai  Prof. Nguyen Xuan Nhiem  Dr. Pham Hai Yen  Nguyen Huy Hoang  Dr. Do Thi Trang  Dr. Duong Thi Dung  Prof. Nguyen Van Tuyen  Dr. Le Tuan Anh
Affiliation:1. Institute of Marine Biochemistry, Vietnam Academy of Science and Technology, VAST), 18 Hoang Quoc Viet, Cau Giay, 10072 Hanoi, Vietnam;2. Graduate University of Science and Technology, VAST, 18 Hoang Quoc Viet, Cau Giay, 10072 Hanoi, Vietnam

Hai Phong University of Medicine And Pharmacy, 72A Nguyen Binh Khiem, Ngo Quyen, 180000 Hai Phong, Vietnam;3. Institute of Marine Biochemistry, Vietnam Academy of Science and Technology, VAST), 18 Hoang Quoc Viet, Cau Giay, 10072 Hanoi, Vietnam

Graduate University of Science and Technology, VAST, 18 Hoang Quoc Viet, Cau Giay, 10072 Hanoi, Vietnam;4. Institute of Chemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, 10000 Hanoi, Vietnam;5. Vietnam National Museum of Nature, VAST, 18 Hoang Quoc Viet, Cau Giay, 10000 Hanoi, Vietnam

Abstract:Four undescribed phenolic glycosides including three stilbene derivatives ( 1 and 3 ) and sodium salt of 3 ( 2 ), and a chalcone glycoside ( 4 ), together with thirteen known compounds ( 5 – 17 ) were isolated from the leaves of Syzygium attopeuense (Gagnep.) Merr. & L.M.Perry. Their chemical structures were elucidated to be (Z)-gaylussacin ( 1 ), 6′′-O-galloylgaylussacin sodium salt ( 2 ), 6′′-O-galloylgaylussacin ( 3 ), 4′-O-[β-D-glucopyranosyl-(1→6)-glucopyranosyl]oxy-2′-hydroxy-6′-methoxydihydrochalcone ( 4 ), gaylussacin ( 5 ), pinosilvin 3-O-β-D-glucopyranoside ( 6 ), myricetin-3-O-(2′′-O-galloyl)-α-L-rhamnopyranoside ( 7 ), myricetin-3-O-(3′′-O-galloyl)-α-L-rhamnopyranoside ( 8 ), myricetin-3-O-α-L-rhamnopyranoside ( 9 ), quercitrin ( 10 ), myricetin-3-O-β-D-glucopyranoside ( 11 ), myricetin-3-O-β-D-galactopyranoside ( 12 ), quercetin 3-O-α-L-arabinopyranoside ( 13 ), myricetin-3-O-2′′-O-galloyl)-α-L-arabinopyranoside ( 14 ), (+)-gallocatechin ( 15 ), (−)-epigallocatechin ( 16 ), and 3,3’,4’-trimethoxyellagic acid 4-O-β-D-glucopyranoside ( 17 ) by the analysis of HR-ESI-MS, 1D and 2D NMR spectra in comparison with the previously reported data. Compounds 1–3 , 5 , and 6 significant inhibition of NO production in LPS-activated RAW264.7 cells, with IC50 values ranging from 18.37±1.38 to 35.12±2.53 μM, compared to a positive control (dexamethasone) with an IC50 value of 15.37±1.42 μM.
Keywords:Syzygium attopeuense  Myrtaceae  nitric oxide inhibitor  gaylussacin derivative  phenolic glycoside
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