Institute of Chemistry, Vietnam Academy of Science and Technology, Hanoi, Vietnam.
Nat Prod Res. 2012;26(14):1296-302. doi: 10.1080/14786419.2011.570761. Epub 2011 Nov 11.
Two new aporphine alkaloids: 8-hydroxy-9-methoxy-1,2-methylenedioxyaporphine (1) and 8-hydroxy-3,9-dimethoxy-1,2-methylenedioxyaporphine (2) were isolated from the ethyl acetate extract of Fissistigma poilanei along with five known compounds: oxocrebanine (3), kuafumine (4), (2R,3R)-3',4',5,7-tetrahydroxydihydroflavonol-3-O-α-L-rhamnopyranoside (5), (+)-catechin 3-O-α-L-rhamnopyranoside (6) and quercetine 3,7-dimethoxy-3'-O-α-L-rhamnopyranosyl-(1 → 2)-β-D-glucopyranoside (7). These two new aporphine alkaloids exhibited a moderate cytotoxic activity against four human cancer cell lines (KB, Hep-G2, MCF-7, LU) as well as antimicrobial activity against Lactobacillus fermentum, Enterococcus faecium, Staphylococcus aureus and Bacillus subtillis.
8-羟基-9-甲氧基-1,2-亚甲二氧基阿朴啡(1)和 8-羟基-3,9-二甲氧基-1,2-亚甲二氧基阿朴啡(2),以及 5 个已知化合物:氧化刻叶紫堇碱(3)、卡枯定(4)、(2R,3R)-3',4',5,7-四羟基二氢黄酮醇-3-O-α-L-鼠李吡喃糖苷(5)、(+)-儿茶素 3-O-α-L-鼠李吡喃糖苷(6)和槲皮素 3,7-二甲氧基-3'-O-α-L-鼠李吡喃糖基-(1 → 2)-β-D-吡喃葡萄糖苷(7)。这两个新的阿朴啡类生物碱对 4 个人类癌细胞系(KB、Hep-G2、MCF-7、LU)表现出中等的细胞毒性活性,并且对乳酸杆菌、屎肠球菌、金黄色葡萄球菌和枯草芽孢杆菌具有抗菌活性。