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几种天然吡喃酮衍生物的抗肿瘤活性分析 被引量:1

Anti-tumor Activity Anaysis of Several Natural Pyrones Derivatives
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摘要 通过对几种天然吡喃酮衍生物的抗肿瘤活性分析,获得具有较强抗肿瘤活性的该类化合物。利用MTT法检测6种结构经修饰与改造的天然吡喃酮类化合物对多种肿瘤细胞的细胞毒性,结果显示化合物LiQ-1与LiH-Ⅳ-80的抗肿瘤活性最为显著。利用化合物LiQ-1分析其对人红白血病K562细胞的生长影响,结果呈剂量依赖关系。通过对化合物的结构分析比较证明,对于化合物LiH-IV-80、LiH-IV-50-2和LiH-III-122-2,在7-位形成的内酯环对抑制肿瘤细胞增殖有着重要的影响,而对于化合物LiQ-1、LiQ-2和LiQ-4,4-位OH对化合物的抗肿瘤活性影响较大。 Natural pyrones derivatives with stronger anti-tumor activity were gained through antitumor activity analysis of several such compounds.MTT was used to detect the cytotoxicity of 6natural pyrone compounds on tumor cells after structural modification and reconstruction.The results show that the antitumor activity of LiQ-1and LiH-Ⅳ-80 is significantly strong.LiQ-1was used to analyze its infleunce on erythroleukemia K562 cell growth,and the result presented dose-dependent relaitonship.Through analysis and comparison of compound structure,it is proven that for LiH-IV-80,LiH-IV-50-2and LiH-III-122-2,lactonic ring formed in 7-position plays an important role on tumor inhibition cell proliferation.For LiQ-1,LiQ-2and LiQ-4,4-position OH has a great affect on tumor activity.
出处 《浙江理工大学学报(自然科学版)》 2016年第1期99-102,115,共5页 Journal of Zhejiang Sci-Tech University(Natural Sciences)
基金 国家自然科学基金项目(81272687) 浙江省生物学重中之重学科开放基金项目(11610032211201/002/008)
关键词 天然吡喃酮 结构修饰 MTT法 抗肿瘤活性 natural pyrone structural modification MTT anti-tumor activity
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  • 1苗丽君,王静.Akt与肿瘤的研究进展[J].国外医学(生理病理科学与临床分册),2004,24(5):406-409. 被引量:38
  • 2张冬松,高慧媛,吴立军.橙皮苷的药理活性研究进展[J].中国现代中药,2006,8(7):25-27. 被引量:94
  • 3BANSKOT A H, TEZUKA Y, PRASAIN J K, et al. Chemical constituents of brazilian propolis and their cytotoxic activities[J]. J Nat Prod, 1998, 61 ( 7 ) : 896 - 900.
  • 4BUCKHEIT R W Jr, FLIAKAS-BOLTZ V, DON DECKER W, et al, Comparative anti-HIV evaluation of diverse HIV-l-specific reverse transcriptase inhibitor-resistant virus isolates demonstrates the existence of distinct phenotypic subgroups [ J ]. Antiviral Res, 1995,26(2) :117- 132.
  • 5BERGMANN R, GERICKE R. Synthesis and antihypertensive activity of 4-( 1, 2-dihydro-2-oxo-1-pyridyl)-2H-1-benzopyran related compounds, new potassium channel activators[J]. J Med Chem, 19901 33(2): 492 - 504.
  • 6KAYE P T, NOCANDA X W. A convenient general synthesis of 3-substituted 2H-chromene derivatives [J].J Chem Soc, Perkin Trans 1, 2002, (10):1318- 1323.
  • 7WANG Y, TAN W, LI W Z, et al. A facile synthetic approach to prenylated flavanone: first total syntheses of(±)-bonanione A and(±)-sophoraflavanone A[J]. J Nat Prod, 2001,64(2) : 196 - 199.
  • 8NIE A H, WANG J, HUANG Z W. Microwave-assisted solution-phase parallel synthesis of 2, 4, 6-trisubstituted pyrimidines[J]. J Comb Chem, 2006, 8 ( 5 ) : 646 - 648.
  • 9NIE A H, HUANG Z W. Microwave-assisted reaction of 2'-hydroxychalcones with hydrazides to synthesize flavanone hydrazone and 4, 5-dihydropyrazole deriva- tives[J] .J Comb Chem, 2006, 8(5) :655 - 658.
  • 10NIE A H, GHOSH S, HUANG Z W. N-(4-chloro-2- phenyl-2H-chromen-3-yl-methylene)-N'- (4-dimethy- lamino benzoyl) hydrazide ethanol solvate [ J ]. Acta Cryst, 2006, E62:01641 - 01642.

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