期刊文献+

香豆素类化合物的抗肿瘤作用研究进展 被引量:21

Research advance of anticancer drugs with coumarin structures
原文传递
导出
摘要 香豆素(coumarins)是具有苯骈α-吡喃酮结构的一类化合物,具有抗肿瘤、抗凝血、抗艾滋病毒、抗炎、抗氧化、抗菌等多种药理活性。近年来研究者发现众多结构特异的香豆素类化合物具有显著的抗肿瘤活性,并报道了其对肿瘤细胞代谢和信号转导通路的影响,充分证明了香豆素类化合物在抗癌药物研发中的重要性。本文以香豆素的基本结构进行分类,综述了天然和合成的香豆素类化合物在抗肿瘤药物方面的研究进展。 Coumarins are a group of compounds with an α-benzopyrone structure, and have shown antitumor, anti-coagulation, anti-HIV, anti-inflammatory, anti-oxidation, anti-bacterial and other pharmacological activities. In recent years, the researchers have isolated or synthesized many structurally specific coumarin derivatives with excellent anti-tumor activity and explored the influence of coumarins on enzymes and cell pathways related to the metabolism of tumor cells, which proves adequately the importance of coumarin skeleton in the research and development of anticancer drugs. In this paper, we reviewed the application of many natural and synthetic coumarins which are classified by classical coumarin structures on exploring new anticancer drugs.
出处 《中国新药杂志》 CAS CSCD 北大核心 2013年第20期2392-2404,共13页 Chinese Journal of New Drugs
关键词 香豆素 抗肿瘤 研究进展 coumarins anti-tumor research advance
  • 相关文献

参考文献96

  • 1LIN HC, TSAI SH, CHEN CS, et al. Structure-activity relation- ship of coumarin derivatives on xanthine oxidase-inhibiting and free radical-scavenging activities [ J ]. Biochem Pharmacol, 2008, 75(6) : 1416 - 1425.
  • 2YANG JY, DELLA-FERA M, BAILE C. Esculetin induces mi- tochondria-mediated apoptosis in 3T3-L1 adipocytes[ J]. Apopto- sis, 2006, 11(8) : 1371 - 1378.
  • 3KOK SH, YEH CC, CHEN ML, et al. Esculetin enhances TRAIL-induced apoptosis through DR5 upregulation in human o- ral cancer SAS cells[J]. Oral Oncol, 2009, 45(12) : 1067 - 1072.
  • 4PARK SS, PARK SK, LIM JH, et al. Esculetin inhibits cell proliferation through the Ras/ERK1/2 pathway in human colon cancer cells[J]. OncolRep, 2011, 25(1): 223-230.
  • 5VZQUEZ R, RIVEIRO ME, VERMEULEN M, et al. Struc- ture-anti-leukemic activity relationship study of ortho-dihydroxy- coumarins in U-937 cells: Key role of the 8-1actone ring in deter- mining differentiation-inducing potency and selective pro-apoptot- ic action[ J. Bioorg Med Chem, 2012, 20(18) : 5537 -5549.
  • 6YOU L, FENG S, AN R, et al. Osthole: a promising lead com- pound for drug discovery from a traditional Chinese medicine (TCM)[J]. Nat Prod Commun, 2009, 4(2): 297 -302.
  • 7HUNG CM, KUO DH, CHOU CH, et al. Osthole suppresses hepatocyte growth factor (HGF) -induced epithelial-mesenchymal transition via repression of the c-Met/Akt/mTOR pathway in hu- man breast cancer ceils [ J ]. J Agr Food Chem,2011, 59 ( 17 ) : 9683 - 9690.
  • 8XU X, ZHANG Y, QU D, et al. Osthole suppresses migration and invasion of A549 human lung cancer cells through inhibition of matrix metalloproteinase-2 and matrix metallopeptidase-9 in vitro[J]. MolMedRep, 2012, 6(5): 1018-1012.
  • 9YOU L, AN R, WANG X, et al. Discovery of novel osthole de- rivatives as potential anti-breast cancer treatment[ J]. Bioorg Med Chem Lett, 2010, 20(24): 7426-7428.
  • 10杨加宾,陈莉,苏国强,任宇.蛇床子素二苯乙烯类衍生物的合成及抑制微管蛋白聚合作用[J].中国药科大学学报,2011,42(2):107-111. 被引量:3

二级参考文献50

共引文献48

同被引文献260

引证文献21

二级引证文献238

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