期刊文献+

二苯乙烯衍生物的合成及抗肿瘤活性 被引量:4

Synthesis and antitumor activity of stilbene derivatives
下载PDF
导出
摘要 以甲氧基取代的4’-氨基二苯乙烯与4-溴甲基-5-甲基-1,3-二氧杂环戊烯-2-酮为原料,通过亲核取代反应合成得到了4种新的二苯乙烯衍生物。这些化合物的结构经NMR、IR和元素分析确定。以HeLa、SMMC-7721、BGC-823和A549为受试细胞株,用MTT法测试了这4种化合物的抗肿瘤活性。测试结果表明,这些化合物具有一定的抗肿瘤活性。 Four new stilbene derivatives were synthesized by nucleophilic substitution from substituted 4' -amino stilbene and 4-bro- momethyl-5-methyl-1,3-dioxolene-2-one. The structures of the compounds were characterized by elemental analysis, IR and NMR spectra. The antitumor activities of compounds were determined with MTT method. The results showed that they displayed a distinct cytotoxicity to HeLa,SMMC-7721 ,BGC-823 and A549 cells.
出处 《化学研究与应用》 CAS CSCD 北大核心 2012年第5期773-777,共5页 Chemical Research and Application
关键词 二苯乙烯衍生物 抗肿瘤活性 合成 stilbene derivatives antitumor activity synthesis
  • 相关文献

参考文献10

  • 1Romeo Romagnoli, Pier Giovanni Baraldi, Vincent Remusat,et al. Synthesis and biological evaluation of 2-( 3', 4' ,5' -trimethoxybenzoyl)-3-amino 5-aryl thiophenes as a new class of tubulin inhibitors [ J ]. J Med Chem,2006,49 : 6425 -6428.
  • 2Gosslau A, Chen M, Ho Ci-T. A methoxy derivative of resveratrol analogue selectively induced activation of the mitoehondrial apoptotie pathway in transformed fibroblasts [ J]. British Journal of Cancer,2005,92:513-521.
  • 3Tetsuro Ito, Toshiyuki Tanaka, Munekazu Iinuma, et al. Three new resveratrol oligomers from the stem bark of Vatlea pauciflora[J]. J Nat Prod,2004,67:932-937.
  • 4邹永,张学景,林惠贞.紫檀芪的合成方法[P].CN:200310111885.4,2003-10-27.
  • 5Chang Jang-Yang, Yang Ming-Fang, Chang Chi-Yen, et al. 2-Amino and 2 '-aminocombretastatin derivatives as potent antimitotic agents[J]. J Med Chem,2006 ,49 :6412-6415.
  • 6Mark Cushman, Dhanapalan Nagarathnam, Gopal D. Syn-thesis and evaluation of stilbene and dihydrostilbene derivatives as paotential anticancer agents that inhibit tubulin polymerization[J]. J Med Chem, 1991,34:2579-2588.
  • 7李宝林,王丽,张喜全,等.1,2-二芳基乙烯类化合物的合成[P].cN:200810154963.1,2008-10-30.
  • 8Nunomura Shigeki ,Sen Akiteru. Method for 4-chloromethyl-5- methyl-1,3-dioxolen-2-one production [ P ]. JP 20ff30fCK/76A, 2001-8-28.
  • 9顾中怡,傅磊.抗癌药物Combretastatin A-4及其水溶性衍生物的合成[J].中国新药杂志,2008,17(15):1322-1325. 被引量:5
  • 10Hiroshi Nishida, Tatsuys Fujii, Yoshiaki Abiru, et al. Studies on synthesis of antibacterial agent( NMd41 ). I . Kinetics and Mechanism of the reaction of 4-( bromomethyl)-5-methyl-1,3-dioxol-2-one with 1-substituted piperazine( NM394 ) [ J ]. Bull Chem Soc Jpn, 1994,67 : 1419-1426.

二级参考文献8

  • 1PETTIT GR, SINGH SB, HAMEL E, et al. Isolation and structure of the strong cell growth and tubulin inhibitor combretastatin A-4[J]. Experientia, 1989, 45(2), 209 -211.
  • 2WEST CML, PRICE P. Combretastatin A-4 phosphate [ J]. Anticancer Drugs, 2004, 15 (3) : 179 - 187.
  • 3DARK GG, HILL SA, PRISE VE, et al. Combretastatin A-4, an agent that displays potent and selective toxicity toward tumor vasculature [ J ]. Cancer Res, 1997, 57 ( 11 ) , : 1829 - 1834.
  • 4WOODS JA, HADFIELD JA, PETTIT GR, et al. The interaction with tubulin of a series of stilbenes based on combretastatin A-4 [J].BrJCancer, 1995, 71(4):705-711.
  • 5PETTIT GR, TEMPLE C, NARAYANAN VL, et al. Antineoplastic agents 322. synthesis of combretastatin A-4 prodrugs[ J]. Anticancer Drug Des, 1995, 10(4) :299 -309.
  • 6PETTIT GR, SINGH SB, BOYD MR, et al. Antineoplastic agents. 291. Isolation and synthesis of combretastatins A-4, A-5, and A-6[J]. J Med Chem, 1995, 38(10):1666-1672.
  • 7GAUKROGER K, HADFIELD JA, HEPWORTH LA, et al. Novel syntheses of cis and trans isomers of combretastatin A-4 [ J]. J Org Chem, 2001, 66(24) : 8135 -8138.
  • 8BORREL C, THORET S, CACHET X, et al. New antitubulin derivatives in the combretastatin A4 series: synthesis and biological evaluation[J]. Bioorg Med Chem, 2005, 13( 11 ) :3853 -3864.

共引文献6

同被引文献40

  • 1袁大军,蒋中伟,徐藻,郭锐,王翔,黄文浩,夏安东,褚家如.双光子三维微细加工的进展[J].纳米技术与精密工程,2004,2(1):50-53. 被引量:3
  • 2王少亭,杨永丽,朱惠菊,聂峰梅,宗瑞发,邓玉恒.稀土、2,2’-联吡啶、邻氨基苯基苯甲酸配合物合成、光谱表征及荧光性质[J].光谱学与光谱分析,2006,26(5):933-935. 被引量:11
  • 3朱玉松,罗世能,沈永嘉,俞惠新,陈波,张来国.白藜芦醇类似物的合成[J].有机化学,2006,26(7):958-962. 被引量:17
  • 4邹永,张学景,林慧贞.紫檀芪的合成方法:中国,200 310 111 885.4[P].2004-10-24.
  • 5Deng X H, Mani N S. A one-pot enamine acylation/eon- densation sequence to construct 5,6,7,8-tetrahydro pyrido [ 4,3-d ] pyrimidine: an efficient synthesis of a selective 5 HT2A reeeptor antagonist [ J ]. J Fudan University( Natural Science) ,2012,51 (5) :637-643.
  • 6Herrera A, Martinez A R, Chioua R,et al. A facile synthe- sis of new tetrahydropyrido [ 4,3-d ] pyrimidine derivatives [ J]. Tetrahedron Lett,2006,47(31) :5 463-5 465.
  • 7James F B,John J G,Jason D M,et al. Discovery of 5,6, 7,8-tetrahydropyrido[ 3,4-d] pyrimidine inhibitors of Erk2 [J]. Bioorg Med Chem Lett,2014,24 :2 635-2 639.
  • 8Aronov A M, Baker C, Bemis G W, et al. Flipped out: structure-guided design of selective pyrolylpyrrole ERK inhibitors [ J ]. J Med Chem 2007,50 : 1 280-1 2871.
  • 9Gysin S, Lee S H, Dean N M, et al. Pharmacologic inhibi- tion of PAF→MEK→ EPK signaling elicits pancreatic cancer cell cycle arrest through induced expression of p27Kipl [ J]. Cancer Res ,2005 ;65:4 870-4 780.
  • 10M.G.凯利,J_金凯德,Y.方等.作为P2x7调节剂的双环杂芳基化合物及其应用[P].CN:101442909A,2007-05-27.

引证文献4

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部