检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:刘金彪[1] 辛春伟[1] 陈晓彤[1] 邹敏[1] 卢俊瑞[1] 鲍秀荣[1]
出 处:《天津理工大学学报》2009年第2期1-3,共3页Journal of Tianjin University of Technology
基 金:国家自然科学基金(20376063);天津市自然科学基金(043610511)
摘 要:合成抗癌药物中间体脂肪胺取代的蒽醌类化合物,并对其进行体外抗癌活性测试.以1,4,5,8-四羟基蒽醌隐色体和脂肪胺为原料,在氮气保护下进行缩合反应,然后通过氧化合成目标化合物.对目标化合物利用红外光谱和核磁共振氢谱进行表征.体外抗癌活性测试表明化合物1,4-二[2-(二甲氨基)-乙氨基]-5,8-二羟基蒽醌有较强的抗癌活性.1,4- Bialiphatic amino-5,8-dihydroxy anthraquinones as an intermediate of an anticancer drug were synthesized by the condensation and oxidation of leuco- 1,4,5,8- tetrahydroxyanthraquinone with aliphatic amine. Their structures were determined by FTIR and l H-NMR analysis. Anti-cancer activities of these compounds were roughly tested in vitro. Such 1,4- bi [ 2 ( dimethylamio ) -ethylamino ] - 5,8- dihydroxy-anthraquinone derivates made this a versatile strategy for the lead compound of anti-tumor drug.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:3.128.190.205