Yanli Lu, P. Ma, Mingxue Li, Danyun Chen, Xueyan Zou
{"title":"由2-乙酰吡嗪n4 -苯基硫代氨基脲衍生的主基团镓(III)配合物:合成、晶体结构及生物学评价","authors":"Yanli Lu, P. Ma, Mingxue Li, Danyun Chen, Xueyan Zou","doi":"10.1080/15533174.2014.989585","DOIUrl":null,"url":null,"abstract":"Up to now, main group gallium(III) complexes with thiosemicarbazones have been comparatively rare. Here, a main group six-coordinated gallium(III) complex [Ga(L)2]NO3·H2O (1) (HL = 2-acetylpyrazine N4-phenylthiosemicarbazone) has been synthesized and characterized by elemental analysis, IR and UV/Vis spectroscopy, mass spectrometry, and single-crystal X-ray diffraction. The cytotoxicity data suggest that 1 exhibits significant antiproliferative activity in vitro against three human cancer cells. Its possible apoptotic mechanism has been evaluated in HepG2 cells. 1 induces a dose-dependent apoptosis in HepG2 cells and the apoptosis is associated with reduction of mitochondrial membrane potential.","PeriodicalId":22118,"journal":{"name":"Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2016-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"A Main Group Gallium(III) Complex Derived from 2-Acetylpyrazine N4-phenylthiosemicarbazone: Synthesis, Crystal Structure and Biological Evaluation\",\"authors\":\"Yanli Lu, P. Ma, Mingxue Li, Danyun Chen, Xueyan Zou\",\"doi\":\"10.1080/15533174.2014.989585\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Up to now, main group gallium(III) complexes with thiosemicarbazones have been comparatively rare. Here, a main group six-coordinated gallium(III) complex [Ga(L)2]NO3·H2O (1) (HL = 2-acetylpyrazine N4-phenylthiosemicarbazone) has been synthesized and characterized by elemental analysis, IR and UV/Vis spectroscopy, mass spectrometry, and single-crystal X-ray diffraction. The cytotoxicity data suggest that 1 exhibits significant antiproliferative activity in vitro against three human cancer cells. Its possible apoptotic mechanism has been evaluated in HepG2 cells. 1 induces a dose-dependent apoptosis in HepG2 cells and the apoptosis is associated with reduction of mitochondrial membrane potential.\",\"PeriodicalId\":22118,\"journal\":{\"name\":\"Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-05-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/15533174.2014.989585\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/15533174.2014.989585","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A Main Group Gallium(III) Complex Derived from 2-Acetylpyrazine N4-phenylthiosemicarbazone: Synthesis, Crystal Structure and Biological Evaluation
Up to now, main group gallium(III) complexes with thiosemicarbazones have been comparatively rare. Here, a main group six-coordinated gallium(III) complex [Ga(L)2]NO3·H2O (1) (HL = 2-acetylpyrazine N4-phenylthiosemicarbazone) has been synthesized and characterized by elemental analysis, IR and UV/Vis spectroscopy, mass spectrometry, and single-crystal X-ray diffraction. The cytotoxicity data suggest that 1 exhibits significant antiproliferative activity in vitro against three human cancer cells. Its possible apoptotic mechanism has been evaluated in HepG2 cells. 1 induces a dose-dependent apoptosis in HepG2 cells and the apoptosis is associated with reduction of mitochondrial membrane potential.