Chalcone synthesis, properties and medicinal applications: a review

被引:0
作者
Aluru Rammohan
Julakanti Satyanarayana Reddy
Gundala Sravya
Chittluri Narasimha Rao
Grigory V. Zyryanov
机构
[1] Ural Federal University,Department of Organic and Biomolecular Chemistry
[2] Sri Venkateswara University,Department of Chemistry
[3] National Health Research Institute,Ural Division of the Russian Academy of Sciences
[4] I. Ya. Postovskiy Institute of Organic Synthesis,undefined
来源
Environmental Chemistry Letters | 2020年 / 18卷
关键词
Antidiabetic activity; Chalcones; Chemopreventors; Claisen–Schmidt condensation; Fluorescent material; Witting reaction;
D O I
暂无
中图分类号
学科分类号
摘要
Chalcone is an aromatic ketone that forms the central core of many important biological compounds, which are known as chalcones. Chalcones are the biogenetic precursors of flavonoids and isoflavonoids, which are abundant in plants. Chalcones are active lead molecules in medicinal chemistry for the discovery of new drugs. Here, we review properties, biosynthesis and structural diversity of natural chalcones. Then, we present the synthesis of chalcones and their biological activities with focus on structure–activity relationships. Pharmaceutically important and patented chalcones are also discussed.
引用
收藏
页码:433 / 458
页数:25
相关论文
共 580 条
  • [1] Abonia R(2018)(E)-3-[3-(2-Butoxyquinolin-3-yl) acryloyl]-2-hydroxy-4H-chromen-4-one Molbank 3 1001-140
  • [2] Gutierrez L(2007)Flavonoids, Chemistry, Biochemistry and Applications By Ø. M. Andersen (University of Bergen) and K. R. Markham (Industrial Research Ltd.). CRC Press/Taylor & Francis, Boca Raton. 2006. xiv + 1237 pp. 7 × 101/4in. $249.95. ISBN 0-8493-2021-6 Journal of Natural Products 70 140-37
  • [3] Quiroga J(1995)Anticancer and antioxidant activity of synthetic chalcones and related compounds Cancer Lett 97 33-748
  • [4] Insuasty B(2016)Synthesis and biological evaluation of novel bischalcone derivatives as carbonic anhydrase inhibitors Arch Pharm 349 741-922
  • [5] Mata Rachel(2016)Microwave-assisted synthesis and biological evaluation of carbazole-based chalcones, aurones, and flavones Med Chem Res 25 909-9794
  • [6] Anto RJ(2008)Structure-activity relationship of antibacterial chalcones Bioorg Med Chem 16 9790-2797
  • [7] Sukumaran K(1995)Synthesis and pharmacological evaluation of 2′-hydroxychalcones and flavones as inhibitors of inflammatory mediators generation J Med Chem 38 2794-3176
  • [8] Kuttan G(2016)Synthesis and anti-proliferative activity of fluoro-substituted chalcones Bioorg Med Chem Lett 26 3172-6074
  • [9] Rao MNA(2006)Ultrasound accelerated Claisen-Schmidt condensation: a green route to chalcones Appl Surf Sci 252 6071-873
  • [10] Subbaraju V(1997)Activity-guided isolation of constituents of J Nat Prod 60 869-518