摘要
综合应用HP-20、硅胶、ODS、Sephadex LH-20、HW-40和半制备液相等多种色谱学方法对黄花蒿Artemisia annua干燥地上部分水提取物中的化合物进行分离纯化,并根据化合物的理化性质和核磁共振波谱数据进行结构鉴定。结果分离鉴定了15个化合物,分别为vitexnegheteroin M(1)、sibricose A5(2)、securoside A(3)、citrusin D(4)、annphenone(5)、E-melilotoside(6)、马栗树皮素(7)、东莨菪素苷(8)、刺五加苷B1(9)、猫眼草酚苷D(10)、万寿菊素-3-O-β-D-吡喃葡萄糖苷(11)、槲皮素-7-O-β-D-葡萄糖苷(12)、芦丁(13)、芹菜素-6,8-二葡萄糖碳苷(14)、异夏佛塔苷(15),其中化合物1~4为首次从蒿属植物中分离得到。采用LPS诱导小鼠巨噬细胞RAW264.7模型,以抑制炎性细胞因子前列腺素E2(PGE2)的分泌为评价指标对分离得到的化合物进行体外抗炎活性评价。结果显示化合物1,2,8,10~15对LPS诱导小鼠巨噬RAW264.7细胞中PGE2的分泌具有一定的抑制作用。
Chemical constituents were isolated and purified from the water extract of Artemisia annua by column chromatography of HP-20 macroporous resin,silica gel,ODS,Sephadex LH-20,HW-40,and semi-preparative RP-HPLC.Their structures were elucidated by physicochemical properties and spectral analyses.As a result,Fifteen compounds were isolated and identified as vitexnegheteroin M(1),sibricose A5(2),securoside A(3),citrusin D(4),annphenone(5),E-melilotoside(6),esculetin(7),scopoletin-7-O-β-D-glucoside(8),eleutheroside B1(9),chrysosplenol D(10),patuletin-3-O-β-D-glucopyranoside(11),quercetin-7-O-β-D-glucoside(12),rutin(13),apigenin 6,8-di-C-β-D-glucopyranoside(14),isoschaftoside(15),among them,compounds 1-4 were identified from Artemisia for the first time.Additionally,the isolates were evaluated for their inhibitory effects on the production of PGE2 in LPS-simulated RAW264.7 macrophages.The results showed that compounds 1,2,8,and 10-15 could reduce PGE2 levels,to a certain extent.
作者
肖立皓
李海波
黄玉欣
秦大鹏
章晨峰
王振中
于洋
XIAO Li-hao;LI Hai-bo;HUANG Yu-xin;QIN Da-peng;ZHANG Chen-feng;WANG Zhen-zhong;YU Yang(State Key Laboratory of New-tech for Chinese Medicine Pharmaceutical Process,Kanion Pharmaceutical Co.,Ltd.,Lianyungang 222001,China;Institute of Traditional Chinese Medicine and Natural Products,College of Pharmacy,Jinan University,Guangzhou 510632,China;School of Pharmaceutical Sciences,Shenzhen University Health Science Center,Shenzhen 518060,China)
出处
《中国中药杂志》
CAS
CSCD
北大核心
2021年第5期1160-1167,共8页
China Journal of Chinese Materia Medica
基金
国家“重大新药创制”科技重大专项(2018ZX09711001-008-005)
国家自然科学基金重点项目(81630097)。
关键词
青蒿
化学成分
结构鉴定
前列腺素E2
Artemisia annua
chemical constituents
structure elucidation
PGE2