Chalcone synthesis, properties and medicinal applications: a review

被引:242
作者
Rammohan, Aluru [1 ,2 ]
Reddy, Julakanti Satyanarayana [3 ]
Sravya, Gundala [1 ]
Rao, Chittluri Narasimha [2 ]
Zyryanov, Grigory V. [1 ,4 ]
机构
[1] Ural Fed Univ, Dept Organ & Biomol Chem, 19 Mira, Ekaterinburg 620002, Russia
[2] Sri Venkateswara Univ, Dept Chem, Tirupati 517502, Andhra Pradesh, India
[3] Natl Hlth Res Inst, 37 Keyan Rd, Zhunan 35053, Miaoli County, Taiwan
[4] Russian Acad Sci, I Ya Postovskiy Inst Organ Synth, Ural Div, 22 S Kovalevskoy St, Ekaterinburg, Russia
关键词
Antidiabetic activity; Chalcones; Chemopreventors; Claisen-Schmidt condensation; Fluorescent material; Witting reaction; IN-VITRO; GLYCYRRHIZA-INFLATA; BIOLOGICAL EVALUATION; ISOPRENYL FLAVONOIDS; BETA-HYDROXYCHALCONE; ANTIOXIDANT ACTIVITY; LICOCHALCONE-A; SOLVENT-FREE; DERIVATIVES; CONSTITUENTS;
D O I
10.1007/s10311-019-00959-w
中图分类号
O6 [化学];
学科分类号
0703 ;
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:26
相关论文
共 131 条
[1]   (E)-3-[3-(2-Butoxyquinolin-3-yl)acryloyl]-2-hydroxy-4H-chromen-4-one [J].
Abonia, Rodrigo ;
Gutierrez, Luisa ;
Quiroga, Jairo ;
Insuasty, Braulio .
MOLBANK, 2018, (03)
[2]  
Agrawal P.K, 2013, Carbon-13 NMR of flavonoids
[3]   ANTICANCER AND ANTIOXIDANT ACTIVITY OF SYNTHETIC CHALCONES AND RELATED-COMPOUNDS [J].
ANTO, RJ ;
SUKUMARAN, K ;
KUTTAN, G ;
RAO, MNA ;
SUBBARAJU, V ;
KUTTAN, R .
CANCER LETTERS, 1995, 97 (01) :33-37
[4]   Synthesis and Biological Evaluation of Novel Bischalcone Derivatives as Carbonic Anhydrase Inhibitors [J].
Arslan, Tayfun ;
Celik, Gonca ;
Celik, Habip ;
Senturk, Murat ;
Yayli, Nurettin ;
Ekinci, Deniz .
ARCHIV DER PHARMAZIE, 2016, 349 (09) :741-748
[5]   Microwave-assisted synthesis and biological evaluation of carbazole-based chalcones, aurones and flavones [J].
Ashok, D. ;
Ravi, S. ;
Ganesh, Arram ;
Lakshmi, B. Vijaya ;
Adam, Shaik ;
Murthy, S. D. S. .
MEDICINAL CHEMISTRY RESEARCH, 2016, 25 (05) :909-922
[6]   Structure-activity relationship of antibacterial chalcones [J].
Avila, Hugo Pereira ;
Albino Smania, Elza de Fatima ;
Delle Monache, Franco ;
Junior, Artur Smania .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (22) :9790-9794
[7]   SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF 2'-HYDROXYCHALCONES AND FLAVONES AS INHIBITORS OF INFLAMMATORY MEDIATORS GENERATION [J].
BALLESTEROS, JF ;
SANZ, MJ ;
UBEDA, A ;
MIRANDA, MA ;
IBORRA, S ;
PAYA, M ;
ALCARAZ, MJ .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (14) :2794-2797
[8]  
Baretto M., 2013, Japan Patent, Patent No. [2013-180955A, 2013180955]
[9]  
Borate H. B, 2016, U.S. Patent, Patent No. [9,512,087B2, 9512087]
[10]   Synthesis and anti-proliferative activity of fluoro-substituted chalcones [J].
Burmaoglu, Serdar ;
Algul, Oztekin ;
Anil, Derya Aktas ;
Gobek, Arzu ;
Duran, Gulay Gulbol ;
Ersan, Ronak Haj ;
Duran, Nizami .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2016, 26 (13) :3172-3176