Kang Jie, Tang Yanbo, Liu Quan, Guo Nan, Zhang Jian, Xiao Zhiyan, Chen Ruoyun, Shen Zhufang
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, People's Republic of China.
Department of Cell and Molecular Biology, Research Institute of Orthopedics & Traumatology, Foshan Hospital of TCM, Foshan 528000, People's Republic of China.
Fitoterapia. 2016 Jul;112:197-204. doi: 10.1016/j.fitote.2016.05.011. Epub 2016 May 24.
To find aldose reductase inhibitors, two previously unreported compounds, grandifolias H and I, and five known compounds, including rosmarinic acid and rosmarinic acid derivatives, were isolated from the roots of Salvia grandifolia. A series of rosmarinic acid derivatives was obtained from rosmarinic acid using simple synthetic methods. The aldose reductase inhibitory activity of the isolated and synthesized compounds was assessed. Seven of the tested compounds showed moderate aldose reductase inhibition (IC50=0.06-0.30μM). The structure-activity relationship of aldose reductase inhibitory activity of rosmarinic acid derivatives was discussed for the first time. This study provided useful information that will facilitate the development of aldose reductase inhibitors.
为了寻找醛糖还原酶抑制剂,从大叶鼠尾草的根部分离出两种此前未报道的化合物,大叶鼠尾草素H和I,以及五种已知化合物,包括迷迭香酸和迷迭香酸衍生物。使用简单的合成方法从迷迭香酸中获得了一系列迷迭香酸衍生物。评估了分离和合成化合物的醛糖还原酶抑制活性。七种测试化合物表现出中等程度的醛糖还原酶抑制作用(IC50 = 0.06 - 0.30μM)。首次讨论了迷迭香酸衍生物醛糖还原酶抑制活性的构效关系。本研究提供了有助于醛糖还原酶抑制剂开发的有用信息。