摘要
利用协同前药原理,在穿心莲内酯衍生物的结构上引入硝酸酯,合成了硝酸酯NO供体新化合物9个,以期找到生物利用度更高、抗癌作用更好的新药;目标化合物结构经1HNMR,13CNMR和MS确证.
The mutual prodmg principle was applied to andrographolide derivatives. Nine compounds of NO donors were synthesized in order to find out new medicines of high bioavailability and good anticancer effect. All the target compounds have been identified by ^1H NMR, ^13c NMR and MS spectra.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2005年第11期1386-1391,共6页
Chinese Journal of Organic Chemistry
基金
国家教育部科技司基金(No.[2003]64号-12)资助项目.