摘要
采用硅胶、ODS和大孔树脂等柱色谱分离方法对Anisopus mannii的叶进行分离纯化,通过NMR、HR-ESI-MS等波谱技术鉴定了7个化合物分别为:3β-acetoxylup-20(29)-ene (1),1-acetoxy-2-isopropyl-1-tridecene (2),rutin (3),3,6'-diferuloylsucrose (4),3-O-β-D-glucopyranosyl-3-β-hydroxyolean-12-en-28-oic acid 28-O-[α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranosyl] ester (5),conduritol A (6),hoyacarnoside I (7)。同时采用B16细胞为黑色素抑制的筛选模型,筛选了所有化合物的黑色素抑制活性和细胞毒性。结果显示:所有化合物均具有不同程度的抑制黑色素生成的活性,其中化合物5显示出最优活性[30μmol/L给药浓度,黑色素含量:(27. 4±3. 5)%,细胞存活率:(54. 9±5. 6)%],可以作为美白剂进一步开发。
The phytochemical studies on the leaves of Anisopus mannii led to the isolation of seven compounds by silica gel,ODS,DIAION HP-20,Sephadex LH-20colunmn chromatographer,their structures were elucidated on the basis of the spectroscopic analyses(NMR,HRMS)and the comparisons with the literatures as3β-acetoxylup-20(29)-ene(1),1-acetoxy-2-isopropyl-1-tridecene(2),rutin(3),3,6′-diferuloylsucrose(4),3-O-β-D-glucopyranosyl-3-β-hydroxyolean-12-en-28-oic acid28-O-[α-L-rhamnopyra-nosyl-(1→2)-β-D-glucopyranosyl]ester(5),conduritol A(6),hoyacarnoside I(7).Meanwhile,the isolated compounds were evaluated for their inhibitory activities against melanogensis in B16melanoma cells,as the results,all compounds exhibited melanogenesis-inhibitory activity and compound5showed a strongest activity(Melanin content:(27.4±3.5)%,Cell Viability:(54.9±5.6)%with a concentration of30μmol/L)which could be further developed.
作者
叶峰
吕青林
祝婉芳
冯锋
张杰
YE Feng;LYU Qinglin;ZHU Wanfang;FENG Feng;ZHANG Jie(School of Traditional Chinese Medcine,China Pharmaceutical University,Nanjing 211198;Jiangsu Food and Pharmaceutical Science College,Huaian,223003,China)
出处
《中国药科大学学报》
CAS
CSCD
北大核心
2018年第6期676-681,共6页
Journal of China Pharmaceutical University
基金
国家自然科学基金资助项目(No.81703383)
江苏省自然科学基金资助项目(No.BK20170742)
国家基础科学人才培养基金资助项目(No.J1310032)~~