Recent developments with oxazolidinone antibiotics

被引:14
作者
Riedl, B [1 ]
Endermann, R [1 ]
机构
[1] Bayer AG, Pharma Res Ctr, D-42096 Wuppertal, Germany
关键词
antibiotic; DuP-721; enterococci; eperezolid; Gram-positive; linezolid; methicillin-resistant Staphylococcus aureus; methicillin-resistant Streptococcus epidermidis; monoamine oxidase inhibitors; mycobacteria; N-phenyl oxazolidinone; N-pyridyl oxazolidinone; N-thienyl oxazolidinone; oxazolidinone; penicillin-resistant Streptococcus pneumoniae; staphylococci; vancomycin-resistant enterococci;
D O I
10.1517/13543776.9.5.625
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The emerging problems with multiple antibiotic-resistant Gram-positive cocci led to the re-evaluation of an antibacterial class of compounds, the oxazolidinones. During the 1990s, many companies such as Upjohn, Bayer, Zeneca, Roussel Uclaf, Marion Merrell Dow and Glare published their work on antibacterial active oxazolidinones. The primary work in this area started in the 1980s at DuPont. The efforts of these scientists led to N-phenyl and N-heteroaryl oxazolidinones with strong antibacterial activity in vitro and in vivo. The most advanced oxazolidinone, linezolid, discovered by scientists at Upjohn, is currently undergoing Phase III clinical trials.
引用
收藏
页码:625 / 633
页数:9
相关论文
共 79 条
[1]   OXAZOLIDINONES, A NEW CLASS OF SYNTHETIC ANTITUBERCULOSIS AGENT - INVITRO AND INVIVO ACTIVITIES OF DUP-721 AGAINST MYCOBACTERIUM-TUBERCULOSIS [J].
ASHTEKAR, DR ;
COSTAPERIERA, R ;
SHRINIVASAN, T ;
IYYER, R ;
VISHVANATHAN, N ;
RITTEL, W .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1991, 14 (06) :465-471
[2]   Identification of a novel oxazolidinone (U-100480) with potent antimycobacterial activity [J].
Barbachyn, MR ;
Hutchinson, DK ;
Brickner, SJ ;
Cynamon, MH ;
Kilburn, JO ;
Klemens, SP ;
Glickman, SE ;
Grega, KC ;
Hendges, SK ;
Toops, DS ;
Ford, CW ;
Zurenko, GE .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (03) :680-685
[3]  
Barbachyn MR, 1997, [No title captured], Patent No. [5688792 A, 5688792, US 5688792]
[4]  
BARTEL S, 1998, 38 ICAAC SAN DIEG CA
[5]  
BARTEL S, 1997, 37 ICAAC TOR CAN
[6]  
Borthwick AD, 1996, MED CHEM RES, V6, P22
[7]  
Brickner SJ, 1996, CURR PHARM DESIGN, V2, P175
[8]   Synthesis and antibacterial activity of U-100592 and U-100766, two oxazolidinone antibacterial agents for the potential treatment of multidrug-resistant Gram-positive bacterial infections [J].
Brickner, SJ ;
Hutchinson, DK ;
Barbachyn, MR ;
Manninen, PR ;
Ulanowicz, DA ;
Garmon, SA ;
Grega, KC ;
Hendges, SK ;
Toops, DS ;
Ford, CW ;
Zurenko, GE .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (03) :673-679
[9]   INVITRO MICROBIOLOGICAL ACTIVITIES OF DUP-105 AND DUP-721, NOVEL SYNTHETIC OXAZOLIDINONES [J].
BRUMFITT, W ;
HAMILTONMILLER, JMT .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1988, 21 (06) :711-720
[10]   On the target of a novel class of antibiotics, oxazolidinones, active against multidrug-resistant Gram-positive bacteria [J].
Burghardt, H ;
Schimz, KL ;
Müller, M .
FEBS LETTERS, 1998, 425 (01) :40-44