Bis-coumarin Derivatives and their Biological Activities

被引:90
作者
Ren, Qing-Cheng [1 ]
Gao, Chuan [1 ]
Xu, Zhi [1 ]
Feng, Lian-Shun [1 ]
Liu, Ming-Liang [2 ,3 ,4 ]
Wu, Xiang [1 ]
Zhao, Feng [1 ]
机构
[1] WuXi AppTec, Wuhan, Hubei, Peoples R China
[2] Wuhan Univ Technol, Int Sch Mat Sci & Engn, Key Lab Adv Technol Mat Synth & Proc, Wuhan, Hubei, Peoples R China
[3] Chinese Acad Med Sci, Inst Med Biotechnol, Beijing 100050, Peoples R China
[4] Peking Union Med Coll, Beijing 100050, Peoples R China
关键词
Bis-coumarin; anti-bacterial; antitumor; antiviral; hybrid compounds; structure-activity relationships; HIV-1 INTEGRASE INHIBITION; BISCOUMARIN DERIVATIVES; MOLECULAR DOCKING; IN-VITRO; CRYSTAL-STRUCTURE; DIHYDROPYRAN DERIVATIVES; ANTIINFLAMMATORY ACTIVITY; ANTIBACTERIAL ACTIVITIES; ANTITUMOR ACTIVITIES; MANNICH-BASES;
D O I
10.2174/1568026618666180221114515
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Bis-coumarins have caused great interests in the recent years. These compounds exhibit diverse biological activities which are ascribed to their ability to exert noncovalent interactions with the various active sites in organisms. Some of them such as dicoumarolum and dicoumarol were approved for therapeutic purposes in clinical practice. Encouraged by the above facts, numerous bis-coumarin derivatives have been synthesized and screened for their biological activities, and many of them showed promising potency. This review is focused on the biological potential of bis-coumarin derivatives with particular mention of those exhibiting antibacterial, anticoagulant, anti-inflammatory, antiviral, anti-parasite and antitumor activities, and their structure-activity relationships are also discussed.
引用
收藏
页码:101 / 113
页数:13
相关论文
共 123 条
[91]   Structure-Activity Relationships of 3,3′-Phenylmethylene-bis-4-hydroxycoumarins: Selective and Potent Inhibitors of Gram-Positive Bacteria [J].
Petnapapun, Kanokporn ;
Chavasiri, Warinthorn ;
Sompornpisut, Pornthep .
SCIENTIFIC WORLD JOURNAL, 2013,
[92]   Synthesis, biological evaluation and molecular docking of novel chalcone-coumarin hybrids as anticancer and antimalarial agents [J].
Pingaew, Ratchanok ;
Saekee, Amporn ;
Mandi, Prasit ;
Nantasenamat, Chanin ;
Prachayasittikul, Supaluk ;
Ruchirawat, Somsak ;
Prachayasittikul, Virapong .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 85 :65-76
[93]   Microwave assisted synthesis of dihydrobenzo[4,5]imidazo[1,2-a]pyrimidin-4-ones; synthesis, in vitro antimicrobial and anticancer activities of novel coumarin substituted dihydrobenzo[4,5]imidazo [1,2-a]pyrimidin-4-ones [J].
Puttaraju, Kallimeledoddi B. ;
Shivashankar, Kalegowda ;
Chandra ;
Mahendra, M. ;
Rasal, Vijaykumar P. ;
Vivek, Ponnuru N. Venkata ;
Rai, Khushboo ;
Chanu, Maibam Beebina .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2013, 69 :316-322
[94]   New Biscoumarin Derivatives: Synthesis, Crystal Structure, Theoretical Study and Antibacterial Activity against Staphylococcus aureus [J].
Qu, Di ;
Li, Jing ;
Yang, Xiao-Hui ;
Zhang, Zi-Dan ;
Luo, Xiao-Xing ;
Li, Ming-Kai ;
Li, Xia .
MOLECULES, 2014, 19 (12) :19868-19879
[95]   New tuberculosis drug leads from naturally occurring compounds [J].
Quan, Diana ;
Nagalingam, Gayathri ;
Payne, Richard ;
Triccas, James A. .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2017, 56 :212-220
[96]  
Rahim F, 2017, J CHEM SOC PAKISTAN, V39, P79
[97]   "MCR-Click" synthesis of coumarin-tagged macrocycles with large Stokes shift values and cytotoxicity against human breast cancer cell line MCF-7 [J].
Raj, P. Jithin ;
Bahulayan, D. .
TETRAHEDRON LETTERS, 2017, 58 (22) :2122-2126
[98]   Synthesis and biological evaluation of chalcone, dihydrochalcone, and 1,3-diarylpropane analogs as anti-inflammatory agents [J].
Reddy, Mopur Vijaya Bhaskar ;
Hung, Hsin-Yi ;
Kuo, Ping-Chung ;
Huang, Guan-Jhong ;
Chan, Yu-Yi ;
Huang, Shiow-Chyn ;
Wu, Shwu-Jen ;
Morris-Natschke, Susan L. ;
Lee, Kuo-Hsiung ;
Wu, Tian-Shung .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2017, 27 (07) :1547-1550
[99]   Synthesis and antitumor evaluation of some new biscarboxamidocoumarin and chromene derivatives [J].
Refat, Hala M. ;
Fadda, A. A. ;
Kamal, Shimaa .
JOURNAL OF THE IRANIAN CHEMICAL SOCIETY, 2015, 12 (05) :845-854
[100]   Development of novel furanocoumarin dimers as potent and selective inhibitors of CYP3A4 [J].
Row, E ;
Brown, SA ;
Stachulski, AV ;
Lennard, MS .
DRUG METABOLISM AND DISPOSITION, 2006, 34 (02) :324-330