Wang Zhi-Bin, Zhai Ya-Dong, Ma Zhen-Ping, Yang Chun-Juan, Pan Rong, Yu Jia-Li, Wang Qiu-Hong, Yang Bing-You, Kuang Hai-Xue
Key Laboratory of Chinese Materia Medica (Ministry of Education), Heilongjiang University of Chinese Medicine, 24 Heping Road, Harbin 150040, P. R. China, (phone: +86-451-82193001; fax: +86-451-82110803).
Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.
Chem Biodivers. 2015 Oct;12(10):1575-84. doi: 10.1002/cbdv.201400371.
Four new cycloartane triterpenes, named huangqiyegenins V and VI and huangqiyenins K and L (1-4, resp.), together with nine known triterpenoids, 5-13, and eight flavonoids, 14-21, were isolated from a 70%-EtOH extract of Astragalus membranaceus leaves. The structures of the new compounds were elucidated by detailed spectroscopic analyses, and the compounds were identified as (9β,11α,16β,20R,24S)-11,16,25-trihydroxy-20,24-epoxy-9,19-cyclolanostane-3,6-dione (1), (9β,16β,24S)-16,24,25-trihydroxy-9,19-cyclolanostane-3,6-dione (2), (3β,6α,9β,16β,20R,24R)-16,25-dihydroxy-3-(β-D-xylopyranosyloxy)-20,24-epoxy-9,19-cyclolanostan-6-yl acetate (3), and (3β,6α,9β,16β,24E)-26-(β-D-glucopyranosyloxy)-16-hydroxy-3-(β-D-xylopyranosyloxy)-9,19-cyclolanost-24-en-6-yl acetate (4). All isolated compounds were evaluated for their inhibitory activities against LPS-induced NO production in RAW264.7 macrophage cells. Compounds 1-3, 14, 15, and 18 exhibited strong inhibition on LPS-induced NO release by macrophages with IC50 values of 14.4-27.1 μM.
从膜荚黄芪叶的70%乙醇提取物中分离出4个新的环阿尔廷烷三萜,分别命名为黄芪根苷V和VI以及黄芪苷K和L(分别为1-4),还有9个已知的三萜类化合物(5-13)和8个黄酮类化合物(14-21)。通过详细的光谱分析阐明了新化合物的结构,这些化合物被鉴定为(9β,11α,16β,20R,24S)-11,16,25-三羟基-20,24-环氧-9,19-环羊毛甾烷-3,6-二酮(1)、(9β,16β,24S)-16,24,25-三羟基-9,19-环羊毛甾烷-3,6-二酮(2)、(3β,6α,9β,16β,20R,24R)-16,25-二羟基-3-(β-D-吡喃木糖氧基)-20,24-环氧-9,19-环羊毛甾烷-6-基乙酸酯(3)和(3β,6α,9β,16β,24E)-26-(β-D-吡喃葡萄糖氧基)-16-羟基-3-(β-D-吡喃木糖氧基)-9,19-环羊毛甾-24-烯-6-基乙酸酯(4)。对所有分离得到的化合物进行了抗RAW264.7巨噬细胞中脂多糖诱导的一氧化氮产生的抑制活性评价。化合物1-3、14、15和18对巨噬细胞脂多糖诱导的一氧化氮释放表现出强烈抑制作用,IC50值为14.4-27.1 μM。