Oxazolidinones as versatile scaffolds in medicinal chemistry

被引:42
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
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
相关论文
共 176 条
[1]   Efficient synthesis and anti-enteroviral activity of 9-arylpurines [J].
Aguado, Leire ;
Canela, Maria-Dolores ;
Thibaut, Hendrik Jan ;
Priego, Eva-Maria ;
Camarasa, Maria-Jose ;
Leyssen, Pieter ;
Neyts, Johan ;
Perez-Perez, Maria-Jesus .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2012, 49 :279-288
[2]  
Al-Tannak NF, 2017, SCI PHARM, V85, DOI 10.3390/scipharm85040034
[3]   Novel Linezolid analogues with antiparasitic activity against Hymenolepis nana [J].
Alcantar-Zavala, Eleazar ;
Hernandez-Guevara, Esteban ;
Ochoa-Teran, Adrian ;
Montes-Avila, Julio ;
Estrada-Zavala, Edgar A. ;
Salazar-Medina, Alex J. ;
Alday, Efrain ;
Cabrera, Alberto ;
Aguirre, Gerardo ;
Miranda-Soto, Valentin ;
Velazquez, Carlos ;
Diaz-Camacho, Sylvia P. ;
Medina-Franco, Jose L. .
BIOORGANIC CHEMISTRY, 2020, 105
[4]   Discovery of novel bis-oxazolidinone compounds as potential potent and selective antitubercular agents [J].
Ang, Wei ;
Ye, Weiwei ;
Sang, Zitai ;
Liu, Yuanyuan ;
Yang, Tao ;
Deng, Yong ;
Luo, Youfu ;
Wei, Yuquan .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2014, 24 (06) :1496-1501
[5]  
[Anonymous], 2020, WHO CONSOLIDATED GUI
[6]   4,5-disubstituted oxazolidinones: High affinity molecular effectors of RNA function [J].
Anupam, Rajaneesh ;
Nayek, Abhijit ;
Green, Nicholas J. ;
Grundy, Frank J. ;
Henkin, Tina M. ;
Means, John A. ;
Bergmeier, Stephen C. ;
Hines, Jennifer V. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (12) :3541-3544
[7]   5-(Carbamoylmethylene)-oxazolidin-2-ones as a Promising Class of Heterocycles Inducing Apoptosis Triggered by Increased ROS Levels and Mitochondrial Dysfunction in Breast and Cervical Cancer [J].
Armentano, Biagio ;
Curcio, Rosita ;
Brindisi, Matteo ;
Mancuso, Raffaella ;
Rago, Vittoria ;
Ziccarelli, Ida ;
Frattaruolo, Luca ;
Fiorillo, Marco ;
Dolce, Vincenza ;
Gabriele, Bartolo ;
Cappello, Anna Rita .
BIOMEDICINES, 2020, 8 (02)
[8]   Synthesis of oxazolidinone from enantiomerically enriched allylic alcohols and determination of their molecular docking and biologic activities [J].
Atmaca, Ufuk ;
Kaya, Ruya ;
Karaman, Halide Sedef ;
Celik, Murat ;
Gulcin, Ilhami .
BIOORGANIC CHEMISTRY, 2019, 88
[9]   Synthesis and antibacterial bioactivities of cationic deacetyl linezolid amphiphiles [J].
Bai, Peng-Yan ;
Qin, Shang-Shang ;
Chu, Wen-Chao ;
Yang, Yi ;
Cui, De-Yun ;
Hua, Yong-Gang ;
Yang, Qian-Qian ;
Zhang, En .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2018, 155 :925-945
[10]   Oxazolidinone structure-activity relationships leading to linezolid [J].
Barbachyn, MR ;
Ford, CW .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (18) :2010-2023