Oxazolidinones as versatile scaffolds in medicinal chemistry

被引:30
作者
Fernandes, Guilherme Felipe Santos [1 ]
Scarim, Caue Benito [2 ]
Kim, Seong-Heun [1 ,3 ]
Wu, Jingyue [1 ]
Castagnolo, Daniele [1 ]
机构
[1] UCL, Dept Chem, 20 Gordon St, London WC1H 0AJ, England
[2] Sao Paulo State Univ, Sch Pharmaceut Sci, Dept Drugs & Med, BR-14800903 Araraquara, Brazil
[3] Kings Coll London, Sch Canc & Pharmaceut Sci, 150 Stamford St, London SE1 9NH, England
来源
RSC MEDICINAL CHEMISTRY | 2023年 / 14卷 / 05期
关键词
IN-VITRO ACTIVITY; S RECEPTOR ANTAGONIST; ANTIBACTERIAL ACTIVITY; BENZOXAZINYL-OXAZOLIDINONES; BIOLOGICAL EVALUATION; ESCHERICHIA-COLI; HIGHLY POTENT; DISCOVERY; DESIGN; INHIBITORS;
D O I
10.1039/d2md00415a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxazolidinone is a five-member heterocyclic ring with several biological applications in medicinal chemistry. Among the three possible isomers, 2-oxazolidinone is the most investigated in drug discovery. Linezolid was pioneered as the first approved drug containing an oxazolidinone ring as the pharmacophore group. Numerous analogues have been developed since its arrival on the market in 2000. Some have succeeded in reaching the advanced stages of clinical studies. However, most oxazolidinone derivatives reported in recent decades have not reached the initial stages of drug development, despite their promising pharmacological applications in a variety of therapeutic areas, including antibacterial, antituberculosis, anticancer, anti-inflammatory, neurologic, and metabolic diseases, among other areas. Therefore, this review article aims to compile the efforts of medicinal chemists who have explored this scaffold over the past decades and highlight the potential of the class for medicinal chemistry.
引用
收藏
页码:823 / 847
页数:25
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