Linezolid, the first oxazolidinone antibacterial agent

被引:140
作者
Leach, Karen L. [1 ]
Brickner, Steven J. [2 ]
Noe, Mark C. [1 ]
Miller, Paul F. [1 ]
机构
[1] Pfizer Inc, Global Res & Dev, Groton, CT 06340 USA
[2] SJ Brickner Consulting LLC, Ledyard, CT USA
来源
PHARMACEUTICAL SCIENCE TO IMPROVE THE HUMAN CONDITION: WINNERS AND FINALIST CANDIDATES OF THE PRIX GALIEN USA, INTERNATIONAL, AND PRO BONO HUMANITARIAN AWARDS 2010 | 2011年 / 1222卷
关键词
Gram-positive; linezolid; antibiotic; GRAM-POSITIVE INFECTIONS; 50S RIBOSOMAL-SUBUNIT; BACTERIAL-INFECTIONS; UNITED-STATES; RESISTANCE; ANTIBIOTICS; U-100592; U-100766; SITE; RNA;
D O I
10.1111/j.1749-6632.2011.05962.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Linezolid (Zyvox (TM)) is the first member of an entirely new class of antibiotics to reach the market in over 35 years; it was approved for use in 2000. A member of the oxazolidinone class of antibiotics, linezolid is highly effective for the treatment of serious Gram-positive infections and has activity that compares favorably with vancomycin for most clinically relevant pathogens. Zyvox is approved for use against serious Gram-positive infections, including those caused by Streptococcus pneumoniae, and the very challenging methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecium organisms. Zyvox inhibits bacterial protein synthesis by binding to 23S rRNA in the catalytic site of the 50S ribosome. It can be administered both orally and intravenously and has good tissue distribution. Recent results have demonstrated that oxazolidinone analogs related to linezolid are effective in treating pulmonary tuberculosis caused by resistant Mycobacterium tuberculosis in animal infection models and suggest additional new therapeutic applications for these antibiotics.
引用
收藏
页码:49 / 54
页数:6
相关论文
共 25 条
[1]  
Brickner SJ, 1996, CURR PHARM DESIGN, V2, P175
[2]   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
[3]   Linezolid (ZYVOX), the first member of a completely new class of antibacterial agents for treatment of serious gram-positive infections [J].
Brickner, Steven J. ;
Barbachyn, Michael R. ;
Hutchinson, Douglas K. ;
Manninen, Peter R. .
JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (07) :1981-1990
[4]   Cross-linking in the living cell locates the site of action of oxazolidinone antibiotics [J].
Colca, JR ;
McDonald, WG ;
Waldon, DJ ;
Thomasco, LM ;
Gadwood, RC ;
Lund, ET ;
Cavey, GS ;
Mathews, WR ;
Adams, LD ;
Cecil, ET ;
Pearson, JD ;
Bock, JH ;
Mott, JE ;
Shinabarger, DL ;
Xiong, LQ ;
Mankin, AS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (24) :21972-21979
[5]   Newer antibacterial drugs for a new century [J].
Devasahayam, Gina ;
Scheld, William M. ;
Hoffman, Paul S. .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2010, 19 (02) :215-234
[6]  
Ford C. W., 2001, Current Drug Targets - Infectious Disorders, V1, P181, DOI 10.2174/1568005014606099
[7]   In vivo activities of U-100592 and U-100766, novel oxazolidinone antimicrobial agents, against experimental bacterial infections [J].
Ford, CW ;
Hamel, JC ;
Wilson, DM ;
Moerman, JK ;
Stapert, D ;
Yancey, RJ ;
Hutchinson, DK ;
Barbachyn, MR ;
Brickner, SJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (06) :1508-1513
[8]   Crystal structure of the oxazolidinone antibiotic linezolid bound to the 50S ribosomal subunit [J].
Ippolito, Joseph A. ;
Kanyo, Zoltan F. ;
Wang, Deping ;
Franceschi, Francois J. ;
Moore, Peter B. ;
Steitz, Thomas A. ;
Duffy, Erin M. .
JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (12) :3353-3356
[9]   United States resistance surveillance results for linezolid (LEADER Program for 2007) [J].
Jones, Ronald N. ;
Ross, James E. ;
Castanheira, Mariana ;
Mendes, Rodrigo E. .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2008, 62 (04) :416-426
[10]   Newer developments in the treatment of Gram-positive infections [J].
Koomanachai, Pornpan ;
Crandon, Jared L. ;
Nicolau, David P. .
EXPERT OPINION ON PHARMACOTHERAPY, 2009, 10 (17) :2829-2843