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含黄胺配体多酸合成、晶体结构及体外抗肿瘤作用

One New Polyoxometalates with Sulfasulfonamide : Synthesis, Crystal Structure and in Vitro Anti-tumor Effect

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【作者】 王路张思琪吴江周百斌

【Author】 Lu Wang 1,2 , Si-Qi Zhang 2 , Wu Jiang 1 , Bai-Bin Zhou 1,* 1 Harbin Normal University, Harbin, Heilongjiang 150025 2 Harbin Institute of Technology, Harbin, Heilongjiang 150090

【机构】 哈尔滨师范大学哈尔滨工业大学

【摘要】 <正>本文合成了含有磺胺配体的Keggin型多金属氧酸盐[{K(C6H10N2O2S)2(H2O)}2(SiW12O40)2]·2H3O+·10H2O(1),并通过元素分析、IR、TG、XPS、183WNMR和单晶X-射线衍射表征其晶体结构。体外实验研究了化合物1的抗肿瘤活性,结果表明,化合物1较配体[σ-SiW12O40]4-和黄胺具有较高的抗肿瘤生物学活性,尤其对人肝癌HepG-2细胞,细胞形态学研究也表明化合物1可诱导癌细胞凋亡,因此,化合物1可成为人类

【Abstract】 Abstract One new Keggin-type polyoxometalates with the ligand of sulfasulfonamide, [{K(C6H10N2O2S)2(H2O)}2(SiW12O40)2]·2H3O+·10H2O(1), has been synthesized. The structure of 1 was analyzed by elemental analysis, IR, TG, XPS, 183 WNMR, and single crystal X-ray diffraction. To evaluate the anti-tumor inhibitory effect of 1 on human cancer lines, in vitro studies were carried out. The results showed that 1 has much higher activities than its parent ligands units [_σ-SiW12O40]4- and sulfasulfonamide, especially with growth inhibitory effect against human liver cancer HepG-2 cells. The cell morphology changes showed that 1 induced apoptosis of tumor cells. Thus, our findings indicated 1 as a potential, new chemopreventive drug for human malignant tumour. Other detailed anti-tumor biological activities also will be studied in follow-up experiments in vitro and in vivo.

【关键词】 多酸体外磺胺抗肿瘤
【基金】 国家自然科学基金项目(No:20971032,21271056)资助;黑龙江省自然科学基金(No:C201037);黑龙江省博士后基金(No:LBH-Z10292)资助
  • 【会议录名称】 中国化学会第五届全国多酸化学学术研讨会论文摘要集
  • 【会议名称】中国化学会第五届全国多酸化学学术研讨会
  • 【会议时间】2013-07-15
  • 【会议地点】中国黑龙江哈尔滨
  • 【分类号】O641.4
  • 【主办单位】中国化学会、国家自然科学基金委员会
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