采用硅胶、聚酰胺层析方法从构棘果中分离得到了4个苯并吡喃异黄酮alpinumisoflavone(1)、4'-O-methylalpinmumisoflavone (2)、4'-O-methylderrone (3)、isoderrone (4)和2个三萜化合物(13α,14β,17 α,20R)-lanosta-7,24-diene-3β-ol(5)、(13α,14β,17α,20R)-lanosta-7,24-diene-3β-O-actate (6).以异黄酮isoderrone为原料进行了结构修饰得到5个新异黄酮衍生物.所有异黄酮均采用噻唑蓝蛋白染色(MTT)法对胃癌细胞SGC-7901的毒性进行了活性筛选,其中化合物4和10对人胃癌SGC-7901肿瘤细胞有中等程度的抑制作用.
Four benzopyranylisoflavones including alpinumisoflavone ( 1 ), 4 ' -O-methylalpinmumisoflavone (2), 4' -O-methylderrone (3), and isoderrone (4) along with two triterpenoid compounds ( 13α, 14β, 17α,20R) - lanosta-7,24-diene-3/3-ol (5) and ( 13α, 14β,17α,20R) -lanosta-7,24-diene-3/3-O-actate (6) were isolated from the fruits of Cudrania cochinchinensis. In addition, five new isoflavone derivatives (7 - 11) were also obtained by the methods of selective methylation, ethylation and O-prenylation using natural isoderrone 4 as a starting material. All isoflavones were tested for the cytotoxicity against SGC-7901 cell lines by MTT method. The result showed that compounds 4 and 10 have moderate cytotoxicity against SGC-7901 cell lines.