期刊文献+

多重靶向的4-取代苯胺喹唑啉类衍生物抗肿瘤活性研究进展 被引量:3

Research Progresses in Antitumor Activity of Multiple Target 4-Substituted Anilinoquinazoline Derivatives
原文传递
导出
摘要 4-取代苯胺喹唑啉类化合物是喹唑啉类酪氨酸激酶抑制剂中活性较高的一类化合物,其对表皮生长因子受体、血管内皮生长因子受体、组蛋白去乙酰化酶等均有抑制作用,已成为抗肿瘤药物的研究热点。综述了近几年多重靶向的4-取代苯胺喹唑啉类化合物抗肿瘤活性的研究进展。 4-Substituted anilinoquinazoline derivatives are a class of compounds with high activities in quinazoline tyrosine kinase inhibitors. They can inhibit the epidermal growth factor receptor (EGFR), vascular endothelial growth factor receptor (VEGFR) and histone deacetylase (HDAC). These compounds have become a research hotspot of antitumor drugs. The advances in research on antitumor bioactivity of 4-substituted anilinoquinazoline derivatives with multiple targets have been reviewed in this paper.
出处 《药学进展》 CAS 2014年第1期25-30,共6页 Progress in Pharmaceutical Sciences
基金 国家自然科学基金资助项目(No.21172265) 江苏省高校"青蓝工程"项目
关键词 4-取代苯胺喹唑啉 人类表皮生长因子受体 血管内皮生长因子受体 组蛋白去乙酰化酶 多靶向 抗肿瘤活性 4-substituted anilinoquinazoline human epidermal growth factor receptor vascular endothelial growth factor receptor histone deacetylase multiple target antitumor bioactivity
  • 相关文献

参考文献5

二级参考文献199

  • 1刘刚,宋宝安,桑维钧,杨松,金林红,丁雄.N-取代芳环-4-氨基喹唑啉类化合物的合成及生物活性研究[J].有机化学,2004,24(10):1296-1299. 被引量:19
  • 2张培权,宋宝安,杨松,金林红,胡德禹,刘刚,薛伟.6-氟-4-(N-芳基)胺基喹唑啉类化合物的微波合成及生物活性研究[J].有机化学,2006,26(9):1275-1278. 被引量:8
  • 3杨松,刘刚,宋宝安,金林红,胡德禹,张素梅.4-(N-取代苯基)氨基喹唑啉类化合物的合成及抗磷酸化活性研究[J].有机化学,2006,26(10):1429-1433. 被引量:9
  • 4李晓晖,李建勋,李世荣,修志龙,西野宪和.环肽类组蛋白去乙酰化酶抑制剂[J].化学进展,2007,19(5):762-768. 被引量:7
  • 5Barker A J, Gibson K H, Grundy W, et al. Studies leading to the identification of ZD 1839 (Iressa^TM) : An orally ative, selective epidermal growth receptor tyrosine kinase inhibitor targeted to the treatment of cancer[ J]. Bioorganic and Medicinal Chemistry Letters, 2001, 11: 1911 - 1914. 被引量:1
  • 6Corbett J W, Pan S L, Markwalder J A, et al. 3,3a - Dihydropyrano [ 4,3, 2 - de ] quinazolin - 2 (1H) - ones are Potent Non - Nucleoside Reverse Transcriptase Inhibitors[ J]. Bioorganic and Medicinal Chemistry Letters, 2001, 11:211 -214. 被引量:1
  • 7Chandrika P M, Yakaiah T, Rao A R R, et al. Synthesis of novel 4, 6 -disubstituted quinazoline derivatives, their anti - inflammatory and anti - cancer activity (cytotoxic) against U937 leukemia cell lines [ J ]. European Journal of Medicinal Chemistry, 2008, 43 (4) : 846 -852. 被引量:1
  • 8Eckhardt M, Langkopf E, Mark M, et al. 8 - (3) - Amiopiperidin - 1 - yl) - 7 - but - 2 - ynyl - 3 - methyl - 1 - (4 - methyl - quinazolin - 2 - ylmethyl) - 3, 7 - dihydropurine - 2,6 - dione ( BI 1356), a Highly potent, selective, Long - Acting, am orally bioavailable DPP- 4 inhibitor for the treatment of type 2 diabetes [ J ]. Journal of Medicinal Chemistry, 2007, 50 : 6450 - 6453. 被引量:1
  • 9Lee J Y, Park Y K, Seo S H, et al. 1,4 - dioxane - fused 4 - anilino- quinazoline as inhibitors of epidermal growth factor receptor kinase[ J]. Archiv der Pharmazie (Weinheim, Germany) , 2001, 334:357 -360. 被引量:1
  • 10Mei H Y, Cui M, Heldsinger A, et al. Inhibitors of protein - RNA complexation that target the RNA : specific recognition of human immunodeficiency virus type 1 TAR RNA by small organic molecules [ J ]. Biochemistry, 1998, 37(40) : 14204 - 14212. 被引量:1

共引文献25

同被引文献67

  • 1袁立,郝金恒,张勇,王玉亚,王晖,陈皎月,宫平.4-(3-氯-4-氟苯胺基)-7-甲氧基-6-[3-(4-吗啉基)丙氧基]喹唑啉的合成[J].中国药物化学杂志,2005,15(1):39-41. 被引量:8
  • 2张伦.磺胺类药物产销现状及趋势[J].中国药房,2005,16(8):571-573. 被引量:16
  • 3Sordel la R, Bell D W, Haber D A, et al. Gefitinib-sensitizing EGFR mutations in lung cancer activate anti-apoptotic pathways [J]. Science, 2004, 305(5 687): 1 163-1 167. 被引量:1
  • 4Wakeling A E, Guy S P, Woodburn J R, et al. ZD1839 (Iressa) an orally active inhibitor of epidermal growth factor signaling with potential for cancer therapy[J]. Cancer Research, 2002, 62(20): 5 749-5 754. 被引量:1
  • 5Vijaychand A, Manjula S N, Bharath E N, et al. Medicinal and biologieal significanee of quinazoline: A highly important seaffold for drug diseovery: A review [J]. International Journal of Pharma & Bio Sciences, 2011, 2(1): 780-809. 被引量:1
  • 6Frank H. Quinazolines and other bieyclie heteroeyclcs, pharmaeeutieal eompositions containing these eompouads as tyrosine kinase inhibitors, and proeesses for preparing them: WO, 2000055141[P]. 2000-09-21. 被引量:1
  • 7Landi L, Tiseo M, Chiari R, et al. Activity of the EGFR- HER2 dual inhibitor afatinib in EGFR-mutant lung cancer patients with acquired resistance to reversible EGFR ty- rosine kinase inhibitors [J]. Ctin Lung Cancer, 2014, 15 (6) : 411-417. 被引量:1
  • 8Assenat E, Azria D, Mollevi C, et al. Dual targeting of HER1/EGFR and HER2 with cetuximab and trastuzumab in patients with metastatic pancreatic cancer after gemcitabine failure: results of the "THERAPY" phase 1-2 trial [J]. On- cotarget, 2015, 6 (14) : 12 796-12 808. 被引量:1
  • 9Pignochino Y, Sarotto I, Peraldo-Neia C, et al. Targeting EGFR/HER2 pathways enhances the antiproliferative effect of gemcitabine in biliary tract and gallbladder carcinomas [J]. BMCCancer, 2010, 10 (33): 631-644. 被引量:1
  • 10Ki J, Arumugam P, Song JM. TIRF high-content assay development for the evaluation of drug efficacy of chemo- therapeutic agents against EGFR-/HER2-positive breast cancer cell lines [J]. Anal Bioanal Chem, 2016, 19 ( 11 ) : 1-6. 被引量:1

引证文献3

二级引证文献5

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