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姜黄素的结构修饰与抗肿瘤研究进展 被引量:1

Study Advances of Structural Modification and Antitumor Activities of Curcumin
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摘要 姜黄素是一种天然的多酚类物质,广泛分布在多种植物中,并具有多种生物活性。但是其存在自身抗肿瘤作用较弱、生物利用度低等缺点,使其临床应用受到了限制。基于此,研究人员对姜黄素进行了大量的结构修饰,以期改善其抗肿瘤活性和成药性。本研究主要对姜黄素的结构修饰及抗肿瘤作用研究进展进行综述,旨在为以后合成高效专一活性的姜黄素衍生物提供依据。 Curcumin was a kind of natural polyphenol widely found in natural plants and had various biological activities. However,anti-tumor effect was weak and bioavailability of curcumin was poor, which had limited the potential clinical application. Based on this fact, researchers had conducted a great deal of structural modifications on curcumin, in order to improve its anti-cancer activities and druggability. In this paper, the research advances of the structural modification of curcumin, as well as anti-cancer activities were reviewed, and those would provide assistances for the subsequent synthesis of curcumin derivatives with high and specific biological activity.
作者 李家庆 LI Jia-qing(Department of Biological Medicine, Changjiang Polytechnic, Wuhan 430064, China)
出处 《化工技术与开发》 CAS 2016年第8期30-35,共6页 Technology & Development of Chemical Industry
关键词 姜黄素 结构修饰 抗肿瘤活性 curcumin structural modification anti-cancer activity
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  • 1郭晓丹,许建华.姜黄素及其衍生物抗肿瘤作用的研究进展[J].海峡药学,2011,23(6):15-18. 被引量:7
  • 2刘红艳,王海燕,叶松,郭静明.姜黄素药理作用及其机制研究进展[J].中国现代医学杂志,2012,22(6):48-51. 被引量:52
  • 3Shi Q, Shih C, Lee H. Novel anti-prostate cancer curcuminanalogues that enhance androgen receptor degradationactivity [J]. Anticancer Agents Med Chem, 2009(8): 904-912.
  • 4Mishra S, Kapoor N, Mubarak A, et al. Differential apoptoticand redox regulatory activities of curcumin and itsderivatives [J]. Free Radic Biol Med, 2005, 38(10): 1353-1360.
  • 5Venkateswarlu S, Ramachandra M S, Subbaraju G V. Synthesisand biological evaluation of polyhydroxycurcuminoids [J].Bioorg Med Chem., 2005, 13(23): 6374-6380.
  • 6Ishida J, Ohtsu H, Tachibana Y, et al. Antitumor agents.Part 214: synthesis and evaluation of curcumin analoguesas cytotoxic agents [J]. Bioorg Med Chem, 2002(11): 3481-3487.
  • 7Lin L, Shi Q, Nyarko A K, et al. Antitumor agents. 250.Design and synthesis of new curcumin analogues as potentialanti-prostate cancer agents[J]. J Med Chem., 2006, 49(13):396-3972.
  • 8Lin L, Shi Q, Su C Y, et al. Antitumor agents 247. New4-ethoxycarbonylethyl curcumin analogs as potentialantiandrogenic agents[J]. Bioorg. Med. Chem., 2006, 14(8):2527-2534.
  • 9Qiu X, Du Y H, Lou B, et al. Synthesis and identification ofnew 4-arylidene curcumin analogues as potential anticanceragents targeting nuclear factor-κB signaling pathway[J]. JMed Chem, 2010, 53 (23): 8260-8273.
  • 10Youssef D, Nichols C E, Cameron T S, et al. Design,synthesis, and cytostatic activity of novel cyclic curcuminanalogues [J]. Bioorg. Med. Chem. Lett., 2007, 17(20):5624-5629.

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