Synthesis and evaluation of novel biaryl oxazolidinones effective against gram-positive bacterial infections

被引：0
|
作者：
Bhawsar, Satish [1 ]
Shaikh, Mohammad [1 ]
Joshi, Sanjeev [1 ]
Mishra, Amit [1 ]
Pavase, Laxmikant [1 ]
Chavan, Vijay [1 ]
Kale, Amol [1 ]
Kayastha, Abhijeet K. [1 ]
Yeole, Ravindra [1 ]
Bhagwat, Sachin [1 ]
Patel, Mahesh [1 ]
机构：
[1] MIDC, Wockhardt Res Ctr, D-4, Aurangabad 431006, Maharashtra, India
来源：
MEDICINAL CHEMISTRY RESEARCH | 2024年 / 33卷 / 10期
关键词：
Biaryl oxazolidinones; antibiotics; gram-positive; MRSA; WCK; 3999; 4603;
D O I：
10.1007/s00044-024-03287-z
中图分类号：
R914 [药物化学];
学科分类号：
100701 ;
摘要：
Oxazolidinones are synthetic antibiotic class of compounds characterized by chemical structure, cyclic carbamate with 'S' configuration of substituent at C-5 position. The synthesis of oxazolidinones has gained increasing interest due to their unique mechanism of action that assures high antibiotic efficiency and low susceptibility to resistance mechanisms. Biaryl oxazolidinones are second-generation oxazolidinone (e.g. Tedizolid) having potency against multidrug-resistant (MDR) gram-positive pathogens including MRSA, VRE, penicillin-resistant S. pneumoniae and linezolid-resistant strains. The current manuscript covers structure activity based synthesis of 21 oxazolidinone analogs prepared through various chemical modifications. These novel biaryl oxazolidinones are prepared with the objective to increase spectrum of activity against multidrug-resistant Gram-positive bacteria. [GRAPHICS] .
引用
收藏
页码：1887 / 1896
页数：10
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