摘要
设计并合成了9种未见文献报道的N-(5-邻氯苯基-2-呋喃甲酰氨基硫羰基)-L-α-氨基酸乙酯衍生物,其结构经IR,1HNMR,MS和元素分析测试确证.MTT法测试结果表明大部分目标化合物对白血病K562细胞系的增殖具有明显的抑制作用.
Nine novel N-[5-(2-chlorophenyl)-2-furamidothiocarbonyl]-L-α-amino acid ethyl esters were designed and synthesized. The structures of all target compounds were confirmed by IR, 1H NMR, MS spectra and elemental analysis. By MTT assay, most target compounds show the activity of restraining the proliferation of K562 cells in vitro.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2008年第3期521-524,共4页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(No.20672073)
上海市重点学科建设(No.T0402)资助项目