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时间:2019-03-07
《槲寄生中的化学成分及其抗肿瘤活性(ⅰ)》由会员上传分享,免费在线阅读,更多相关内容在教育资源-天天文库。
1、万方数据天然产物研究与开发肋tProd肠Dev2009。21:44l444,452文章编号:1001-688012009}03-0441-05槲寄生中的化学成分及其抗肿瘤活性【I)陈柏年,李建宽,杨宫娥+,李青山山西医科大学药学院中药学教研室,太原030001摘要:从槲寄生75%乙醇提取物中分离得到4个化合物,应用波谱学方法鉴定它们的结构为尼克酰胺(1),乙酰胺(2),齐墩果酸(3),口.香树脂醇乙酸酯(4)。其中,化合物1和2为首次从槲寄生属植物中分离得到。采用MTr法对化合物1—4进行体外抗肿瘤活性研究,结果显示化合物1、2和4对H0-8910人卵巢浆液性腺癌、SMMC7721人肝癌、T
2、24人膀胱癌、HepG2人肝癌和SHG人神经胶质瘤细胞系没有细胞毒活性,化合物3则对这五种肿瘤细胞系有显著的抑制作用。关键词:槲寄生;尼克酰胺;齐墩果酸;抗肿瘤;MTT法中图分类号:Q58;R284.2文献标识码:AChemicalConstituentsfromViscumcoloratum(Kom.)NakaiandTheirAntitumorActivities(I)CHENBai—nian,LIJian—kuan,YANGGuan—e+,LIQing-shanDepartmentofTraditionalChineseMedicine,SchoolofPharmaceuticalSc
3、iences,ShanxiMedicalUniversity,Taiyuan030001,ChinaAbstract:Fourchemicalconstituentswereisolatedfromthe75%ethanolextractofViscumcoloratum(Kom.)Nakaiandtheirstructureswereidentified鹊nicotinamide(1),aeetamide(2),oleanolicacid(3),肛锄徊nacetate(4)byspectralmethods.Theantitumoractivitiesofcompounds14werest
4、udiedbyMTTmethod讯vitro.Compounds1,2and4showednocytotoxicactivitiesagainstHO-8910humanovary昵rouBadenoearcinoma.SMMC7721humanhepatoma;T24humanbladdercancer;HepG2humanhepatomaandSHGhumangliomacelllines,andcompound3showedsignificantinhibitoryactivitiesagainstthosefivehumantumorcelllines..Keywords:V/scu
5、mcoloratura(Kom.)Nakai;nicofinamide;oleanolicacid;antitumor;M1-I'IntroductionThemistletoeisaperennialsemiparasiticdwarfshrub,whichcontainsaboutmorethan30species,ofwhich1growinChina。¨.Since1920s,themistletoehasbeenusedforthetreatmentofcancers,suchasbreastCallC—er,gastriccancer,rectalcancer,etc[刘.Wit
6、hthedevel.opmentofcomplementaryoralternativemedicine(CAM)aroundtheworld,thepreparationsmadefrommistletoealebecomingmorepopular.Itisestimatedthattheyearlyexpenditureforthesepreparationsis0.ver$30millioninGermanyalonewithanannualin—ReceivedOctober15,2007;AcceptedJanuary16,2008FoundationItem:Thisworkw
7、assupportedbytheNationalNaturalSci—enceFoundationofChina(30672621)。ShamdProvineialNaturalSci-enceFoundation(20060l1099)andShanx/MedicalUniversity2007StudentInnovationFund.·CorrespondingauthorTel:86-351-4690
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