摘要
基于D1蛋白结构模型,设计并合成了取代苯甲酰胺基丙烯酸乙酯及有关成环化合物嘧啶酮,通过X射线衍射确定了2-芳基-5-乙氧甲酰基-6-甲硫基-4-嘧啶酮的结构.生物活性测定结果表明,部分化合物显示出一定的Hil反应抑制活性.
Based on targets structure and using bio rational molecular design, the title compounds have been designed and synthesized. The structure of pyrimidone 3a was confirmed by X ray. Their Hill inhibitory activities were tested, and it was found that some of them showed good inhibition.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
1998年第12期1946-1949,共4页
Chemical Journal of Chinese Universities
基金
国家自然科学青年基金
天津市自然科学基金