A new symmetrical tetramer oligostilbenoid containing tetrahydrofuran ring from the stem bark of Dryobalanops lanceolata

被引:9
作者
Ahmat, Norizan [1 ]
Wibowo, Agustono [1 ]
Mohamad, Sharifah Aminah Syed [1 ]
Low, Anis Lou Muhammad [1 ]
Sufian, Adila Sahida [2 ]
Yusof, Muhd Izwan Muhd [3 ]
Latip, Jalifah [4 ]
机构
[1] Univ Teknol MARA, Fac Sci Appl, Shah Alam 40450, Selangor Darul, Malaysia
[2] Univ Teknol MARA, Fac Pharm, Kuala Selangor 42300, Selangor, Malaysia
[3] Univ Teknol MARA UiTM, Integrat Pharmacogen Inst iPROMISE, Kuala Selangor 42300, Malaysia
[4] Univ Kebangsaan Malaysia, Sch Chem & Food Technol, Fac Sci & Technol, Bangi 43600, Selangor Darul, Malaysia
关键词
Dipterocarpaceae; oligostilbenoid; malaysianol C; cytotoxicity; antibacterial; Dryobalanops lanceolata; RESVERATROL OLIGOMERS; VITIS-COIGNETIAE; GROWTH; ASSAY;
D O I
10.1080/10286020.2014.938059
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A new tetramer oligostilbenoid possessing tetrahydrofuran ring, malaysianol C (1), was isolated from the acetone extract of the stem bark of Dryobalanops lanceolata, together with four known oligostilbenoids nepalensinol E (2), epsilon-viniferin (3), laevifonol (4), and ampelopsin F (5). The structures of isolated compounds were elucidated on the basis of spectral evidence. The antibacterial activity of the isolated compounds was evaluated using resazurin microtitre-plate assay, whereas the cytotoxic activity was tested using MTT assay. The plausible biogenetic routes of the isolated compounds are also discussed.
引用
收藏
页码:1099 / 1107
页数:9
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