查尔酮异甘草素类化合物的合成及其对子宫颈癌细胞的抑制作用  

Synthesis of Chalcone Isoliquiritigenin Compounds and Its Anti-cervical Cancer Activity

作　　者：杨旭超[1] 王永波[1] 木合布力.阿布力孜 西力扎提.阿不来提 任丙昭 

机构地区：[1]新疆医科大学药学院药物化学有机教研室,乌鲁木齐830011

出　　处：《中国现代应用药学》2016年第1期1-6,共6页Chinese Journal of Modern Applied Pharmacy

基　　金：国家自然科学基金(81260379);新疆研究生科研创新项目(XJGRI2014094)

摘　　要：目的设计并合成查尔酮异甘草素类化合物,并评价其抗子宫颈癌活性。方法利用Claisen-Schmidt反应原理,通过微波固相合成5种目标化合物,并进行结构表征。以Si Ha(人子宫颈鳞癌细胞)和He La(子宫颈癌细胞)细胞株作为体外模型,利用MTT法考察目标化合物对宫颈癌细胞增殖的抑制活性,利用流式细胞仪测定目标化合物对宫颈癌细胞促凋亡作用。结果与结论快速高效合成了5个查尔酮异甘草素类化合物,其结构经~1H-NMR、^(13)C-NMR谱确认。目标化合物能有效抑制宫颈癌细胞增殖,促进宫颈癌细胞凋亡。OBJECTIVE To design and synthesis of chalcone isoliquiritigenin compounds, and evaluate its anti-cervical cancer activity. METHODS Using Claisen-Schmidt reaction principle, by microwave solid-phase synthesis of 5 target compounds, and structural characterization. Si Ha（human cervical squamous cell carcinoma） and He La（cervical cancer cells） cells as in vitro model, using MTT method to study the inhibitory activity of the target compounds on the proliferation of cervical cancer cells, promotion of the apoptosis of cervical cancer cells by flow cytometry. RESULTS CONCLUSION Five chalcone isoliquiritigenin compounds were synthesized and characterized by ^1H-NMR, ^13C-NMR spectra. The target compound could inhibit the proliferation of cervical cancer cells effectively and promote the apoptosis of cervical cancer cells.

关 键 词：查尔酮异甘草素 Claisen-Schmidt反应 微波固相反应 抗子宫颈癌活性 

分 类 号：R284.3[医药卫生—中药学] R285.5[医药卫生—中医学]