Recent advances on biologically active coumarin-based hybrid compounds

被引:32
|
作者
Yildirim, Metin [1 ]
Poyraz, Samet [2 ]
Ersatir, Mehmet [3 ]
机构
[1] Tarsus Univ, Vocat Sch Hlth Serv, Dept Pharm Serv, Tarsus, Mersin, Turkiye
[2] Harran Univ, Dept Analyt Chem, Fac Pharm, Haliliye, Sanliurfa, Turkiye
[3] Cukurova Univ, Arts & Sci Fac, Dept Chem, Seyhan, Adana, Turkiye
关键词
Coumarin hybrids; Coumarin sulfonamide hybrids; Coumarin-triazole hybrids; Coumarin thiazole hybrids; Coumarin-chalcone hybrids; Coumarin-imidazole hybrids; IN-VITRO; MOLECULAR DOCKING; CYTOTOXICITY EVALUATION; CHALCONE DERIVATIVES; DNA-BINDING; DESIGN; ANTIBACTERIAL; SULFONAMIDE; ANTICANCER; INHIBITORS;
D O I
10.1007/s00044-023-03025-x
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Coumarin hybrids have been designed and synthesized as an important new strategy in the field of medicinal chemistry. Coumarin core has been shown to form various compounds to combat several diseases including microbial, cancer, inflammatory, and neurodegenerative disorders. Recently, a number of coumarin-based drugs (e.g., coumadin, acenocoumarol, dicoumarol, phenprocoumon, and novobiocin) have been FDA-approved and are in the clinic, and several coumarin-containing compounds are in clinical trials. Our group classified coumarin-based hybrid compounds into groups showing shared biological activities and discussed their potential therapeutic targets.
引用
收藏
页码:617 / 642
页数:26
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