Department of Pharmacognosy and Chemistry of Natural Products, School of Pharmacy, University of Athens, Panepistimiopolis, Zografou, Athens, Greece.
J Enzyme Inhib Med Chem. 2013 Aug;28(4):704-10. doi: 10.3109/14756366.2012.672415. Epub 2012 May 28.
A new iridoid glycoside, 6'-O-E-caffeoyl-mussaenosidic acid , in addition to one known aglycon, four known triterpenes and one known flavonoid, were isolated from the aerial parts of Scutellaria albida subsp. albida. Furthermore, 12 iridoids with similar structures isolated from Scutellaria sp., were examined for their inhibitory potency on lipoxygenase and lipid peroxidation, as well as their antioxidant activity, in comparison to known antioxidants e.g. caffeic acid, nordihydroguaretic acid (NDGA) and trolox. AAPH, DPPH and soybean lipoxygenase (LOX) assays were used for the tests. This investigation led to interesting observations considering the Structure-Activity Relationship. According to our results, the presence of a p-coumaroyl group optimized and even dramatically changed the biological responses of the investigated iridoids.
从白花黄芩亚种的地上部分分离得到一个新的环烯醚萜糖苷,6'-O-E-咖啡酰毛蕊花糖苷,此外还有一个已知的苷元,四个已知的三萜和一个已知的黄酮类化合物。此外,还对从黄芩属植物中分离得到的 12 个具有相似结构的环烯醚萜进行了抑制脂氧合酶和脂质过氧化以及抗氧化活性的测试,并与已知的抗氧化剂如咖啡酸、去甲二氢愈创木酸(NDGA)和 Trolox 进行了比较。AAPH、DPPH 和大豆脂氧合酶(LOX)测定法用于测试。考虑到结构-活性关系,这项研究得出了有趣的观察结果。根据我们的结果,对 p-香豆酰基的存在优化甚至极大地改变了所研究的环烯醚萜的生物学反应。