Wen Quan, Lu Yan, Chao Zhi, Chen Dao-Feng
Department of Pharmacognosy, School of Pharmacy, Fudan University, Shanghai 201203, PR China.
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, PR China.
Bioorg Med Chem Lett. 2017 Feb 15;27(4):880-886. doi: 10.1016/j.bmcl.2017.01.007. Epub 2017 Jan 6.
Five new (1-5) and twenty-eight known (6-33) triterpenoids were isolated from the roots of Ilex asprella. The structures of the new compounds were elucidated by the detailed spectral analysis. The ursane and oleanane triterpenoids were found to show anticomplement activity with some structure-activity relationships. Several triterpenoids (1-3, 6-7) exhibited potent anticomplement activity with the CH and AP values of 0.058-0.131mg/mL and 0.080-0.444mg/mL, respectively. It was found that caffeoyl group could enhance activity remarkably, followed by coumaroyl and feruloyl group. The 28-carboxyl group was also important to anticomplement activity for the triterpenoids. However, the triterpenoids with lactone ring (4, 9-14) exhibited weak activity and triterpenoid glycosides (5, 23-33) showed no inhibition. The targets of several bioactive triterpenoids in complement activation cascade were identified as well.
从岗梅根中分离得到5个新的三萜类化合物(1-5)和28个已知的三萜类化合物(6-33)。通过详细的光谱分析阐明了新化合物的结构。发现乌苏烷型和齐墩果烷型三萜类化合物具有抗补体活性,并存在一定的构效关系。几种三萜类化合物(1-3、6-7)表现出较强的抗补体活性,其CH值和AP值分别为0.058-0.131mg/mL和0.080-0.444mg/mL。发现咖啡酰基可显著增强活性,其次是香豆酰基和阿魏酰基。28-羧基对三萜类化合物的抗补体活性也很重要。然而,具有内酯环的三萜类化合物(4、9-14)活性较弱,三萜类糖苷(5、23-33)无抑制作用。还确定了几种生物活性三萜类化合物在补体激活级联反应中的作用靶点。