作者:Sun Nam Kim、Jae Yeol Lee、Hyoung Ja Kim、Cha-Gyun Shin、Hokoon Park、Yong Sup Lee
DOI:10.1016/s0960-894x(00)00355-3
日期:2000.8
Caffeoylglucosides, which have a glucose ring as a central linker, were synthesized from methyl D-glucosides, and their anti-HIV-1 activities were tested. Among them, four dicaffeoylglucosides (IC50 = 29.1+/-35.1 microM), 6a, 6b, 9b and 10b, showed HIV-1 integrase inhibitory activity as potent as L-chicoric acid.
由甲基D-葡萄糖苷合成了以葡萄糖环为中心接头的咖啡酰葡萄糖苷,并测试了它们的抗HIV-1活性。其中,四种二咖啡酰葡糖苷(IC50 = 29.1 +/- 35.1 microM),6a,6b,9b和10b,显示出与L-Chicoric acid一样有效的HIV-1整合酶抑制活性。