Nguyen Tan Phat, Tran Thi Thao Vy, Mai Dinh Tri, Le Tien Dung, Phan Nhat Minh, Bui Trong Dat
a Institute of Chemical Technology, Vietnam Academy of Science and Technology , Ho Chi Minh City , Vietnam.
Nat Prod Res. 2015;29(15):1432-6. doi: 10.1080/14786419.2014.1003300. Epub 2015 Feb 4.
From the leaves of Schefflera sessiliflora De P. V., one new C20-gibberellin diterpene 2β,12β-dihydroxygibberellin (12β-hydroxy-GA110 or 2β-hydroxy-GA112) (1), together with three known compounds, trans-tiliroside (2), kaempferol 3-O-β-D-glucuronopyranoside (3), 5-p-trans-coumaroylquinic acid (4), was isolated for the first time from the genus Schefflera by various chromatography methods. Their structures were elucidated by IR, UV, HR-ESI-MS, NMR 1D and 2D experiments and comparison with previous reported data. The α-glucosidase inhibitory activity of all compounds was measured. The isolates (2, 3) showed better α-glucosidase inhibitory activity (IC50 = 134.60, 147.10 μM, respectively) than the standard drug acarbose (IC50 = 214.50 μM).
从无柄鹅掌柴(Schefflera sessiliflora De P. V.)的叶子中,通过各种色谱方法首次从鹅掌柴属植物中分离出一种新的C20-赤霉素二萜2β,12β-二羟基赤霉素(12β-羟基-GA110或2β-羟基-GA112)(1),以及三种已知化合物,反式椴树苷(2)、山柰酚3-O-β-D-葡萄糖醛酸苷(3)、5-p-反式香豆酰奎宁酸(4)。通过红外光谱(IR)、紫外光谱(UV)、高分辨电喷雾电离质谱(HR-ESI-MS)、一维和二维核磁共振实验以及与先前报道数据进行比较,阐明了它们的结构。测定了所有化合物的α-葡萄糖苷酶抑制活性。分离物(2、3)显示出比标准药物阿卡波糖(IC50 = 214.50 μM)更好的α-葡萄糖苷酶抑制活性(IC50分别为134.60、147.10 μM)。