• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利奈唑胺 辉瑞制药有限公司

Linezolid Pharmacia Corp.

作者信息

Barrett J F

机构信息

Pharmaceutical Research and Development Division, Bristol-Myers Squibb Pharmaceutical Research Institute, Wallingford, CT 06492, USA.

出版信息

Curr Opin Investig Drugs. 2000 Oct;1(2):181-7.

PMID:11249571
Abstract

Linezolid is an oxazolidinone developed by Pharmacia (formerly Pharmacia & Upjohn) for the treatment of multi-resistant Gram-positive infections [187765,317456]. It binds to ribosomal 50S subunits, most likely within domain V within the 23S rRNA peptidyl transferase and a secondary interaction with the 30S subunit. This results in inhibition of the initiation of protein translation at an early point, which is probably N-formylmethionyl-tRNA [335843]. No direct action on DNA or RNA synthesis has been observed [220169]. Linezolid resistance due to a 23S rRNA mutation may emerge in Enterococci during therapy with this antimicrobial, and may be associated with clinical failure [368652]. Following FDA approval, linezolid was launched in May 2000 [368526,368652]. In April 2000, the FDA approved linezolid injection, tablets and oral suspension for the treatment of patients with infections caused by Gram-positive bacteria. It is indicated for adults in the treatment of nosocomial pneumonia, community-acquired pneumonia (CAP), complicated and uncomplicated skin and skin structure infections and vancomycin-resistant enterococcus (VRE) infections caused by methicillin-resistant Staphylococcus aureus (MRSA), VRE faecium and penicillin-susceptible Streptococcus pneumoniae [363503]. The FDA, however, did not grant Pharmacia indications for linezolid in the treatment of CAP due to either penicillin-resistant S aureus (PRSA) or MRSA. In May 2000, Merrill Lynch predicted sales for 2000 to be US $50 million, rising to US $760 million in 2004 [366910]. In February 2000, P&U predicted that peak sales of the drug had the potential to reach in excess of US $750 million [358429]. In February 1999, Morgan Stanley Dean Witter predicted sales of US $40 million in 2000 rising to US $275 million in 2005 [319855]. In December 1998, Deutsche Bank predicted sales of US $100 million in 2000 rising to US $300 million in 2002 [316769].

摘要

利奈唑胺是辉瑞公司(原辉瑞制药有限公司)研发的一种恶唑烷酮类药物,用于治疗多重耐药革兰氏阳性菌感染[187765,317456]。它与核糖体50S亚基结合,最有可能在23S核糖体RNA肽基转移酶的结构域V内,并且与30S亚基存在二级相互作用。这导致在早期阶段抑制蛋白质翻译的起始,可能是抑制N-甲酰甲硫氨酰-tRNA[335843]。未观察到对DNA或RNA合成有直接作用[220169]。在使用这种抗菌药物治疗期间,肠球菌可能会因23S rRNA突变而出现利奈唑胺耐药,这可能与临床治疗失败有关[368652]。经美国食品药品监督管理局(FDA)批准后,利奈唑胺于2000年5月上市[368526,368652]。2000年4月,FDA批准利奈唑胺注射剂、片剂和口服混悬液用于治疗由革兰氏阳性菌引起感染的患者。它适用于成人治疗医院获得性肺炎、社区获得性肺炎(CAP)、复杂和非复杂皮肤及皮肤结构感染,以及由耐甲氧西林金黄色葡萄球菌(MRSA)、屎肠球菌VRE和青霉素敏感肺炎链球菌引起的耐万古霉素肠球菌(VRE)感染[363503]。然而,FDA未批准辉瑞公司将利奈唑胺用于治疗由耐青霉素金黄色葡萄球菌(PRSA)或MRSA引起的CAP。2000年5月,美林证券预测2000年的销售额为5000万美元,到2004年将增至7.6亿美元[366910]。2000年2月,辉瑞公司预测该药物的销售峰值有可能超过7.5亿美元[358429]。1999年2月,摩根士丹利添惠预测2000年销售额为4000万美元,到2005年将增至2.75亿美元[319855]。1998年12月,德意志银行预测2000年销售额为1亿美元,到2002年将增至3亿美元[316769]。

相似文献

1
Linezolid Pharmacia Corp.利奈唑胺 辉瑞制药有限公司
Curr Opin Investig Drugs. 2000 Oct;1(2):181-7.
2
Efficacy of linezolid versus comparator therapies in Gram-positive infections.利奈唑胺与对照疗法治疗革兰氏阳性菌感染的疗效比较
J Antimicrob Chemother. 2003 May;51 Suppl 2:ii27-35. doi: 10.1093/jac/dkg251.
3
[New treatment option for gram-positive infections in critically ill patients - overview over linezolid].危重症患者革兰氏阳性菌感染的新治疗选择——利奈唑胺概述
Anasthesiol Intensivmed Notfallmed Schmerzther. 2002 Apr;37(4):199-204. doi: 10.1055/s-2002-25077.
4
Linezolid for the treatment of methicillin-resistant Staphylococcus aureus infections in children.利奈唑胺用于治疗儿童耐甲氧西林金黄色葡萄球菌感染。
Pediatr Infect Dis J. 2003 Sep;22(9 Suppl):S178-85. doi: 10.1097/01.inf.0000087020.75886.93.
5
Have the oxazolidinones lived up to their billing? Future perspectives for this antibacterial class.恶唑烷酮类药物是否名副其实?该抗菌药物类别的未来展望。
Curr Opin Investig Drugs. 2003 Feb;4(2):149-55.
6
Linezolid.利奈唑胺
Indian Pediatr. 2004 Nov;41(11):1129-32.
7
Use of linezolid in children: an overview of recent advances.利奈唑胺在儿童中的应用:近期进展概述。
Expert Rev Anti Infect Ther. 2006 Dec;4(6):947-52. doi: 10.1586/14787210.4.6.947.
8
Linezolid versus vancomycin in the treatment of known or suspected resistant gram-positive infections in neonates.利奈唑胺与万古霉素治疗新生儿已知或疑似耐药革兰氏阳性菌感染的疗效比较
Pediatr Infect Dis J. 2003 Sep;22(9 Suppl):S158-63. doi: 10.1097/01.inf.0000086955.93702.c7.
9
Efficacy and safety of tigecycline compared with vancomycin or linezolid for treatment of serious infections with methicillin-resistant Staphylococcus aureus or vancomycin-resistant enterococci: a Phase 3, multicentre, double-blind, randomized study.替加环素与万古霉素或利奈唑胺治疗耐甲氧西林金黄色葡萄球菌或耐万古霉素肠球菌严重感染的疗效及安全性:一项3期、多中心、双盲、随机研究
J Antimicrob Chemother. 2008 Sep;62 Suppl 1:i17-28. doi: 10.1093/jac/dkn250.
10
Linezolid, the first oxazolidinone antibacterial agent.利奈唑胺,第一个噁唑烷酮类抗菌药物。
Ann N Y Acad Sci. 2011 Mar;1222:49-54. doi: 10.1111/j.1749-6632.2011.05962.x.

引用本文的文献

1
Oxazolidinone antibiotics impair megakaryocyte differentiation from hematopoietic progenitor cells and their maturation into platelets.恶唑烷酮类抗生素可损害造血祖细胞向巨核细胞的分化及其向血小板的成熟。
Antimicrob Agents Chemother. 2024 Oct 8;68(10):e0053324. doi: 10.1128/aac.00533-24. Epub 2024 Sep 19.
2
: insights into epidemiology, virulence, and antimicrobial resistance of a clinically relevant bacterial species.深入了解临床相关细菌物种的流行病学、毒力和抗微生物耐药性。
Clin Microbiol Rev. 2024 Sep 12;37(3):e0011823. doi: 10.1128/cmr.00118-23. Epub 2024 Jun 20.
3
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.
5-(氨甲酰基亚甲基)-恶唑烷-2-酮作为一类有前景的杂环化合物,可通过增加活性氧水平和导致乳腺癌及宫颈癌线粒体功能障碍来诱导细胞凋亡。
Biomedicines. 2020 Feb 18;8(2):35. doi: 10.3390/biomedicines8020035.
4
Pharmacokinetics and pharmacodynamics of linezolid in plasma/cerebrospinal fluid in patients with cerebral hemorrhage after lateral ventricular drainage by Monte Carlo simulation.蒙特卡洛模拟研究脑出血患者侧脑室引流后血浆/脑脊液中利奈唑胺的药代动力学和药效学
Drug Des Devel Ther. 2018 Jun 11;12:1679-1684. doi: 10.2147/DDDT.S168757. eCollection 2018.
5
A validated stability-indicating LC method for the separation of enantiomer and potential impurities of Linezolid using polar organic mode.一种经过验证的稳定性指示液相色谱法,采用极性有机模式分离利奈唑胺的对映体和潜在杂质。
J Pharm Anal. 2012 Aug;2(4):272-278. doi: 10.1016/j.jpha.2012.03.006. Epub 2012 Mar 18.
6
Mevalonate 5-diphosphate mediates ATP binding to the mevalonate diphosphate decarboxylase from the bacterial pathogen .甲羟戊酸 5-二磷酸介导 ATP 与细菌病原体的甲羟戊酸二磷酸脱羧酶结合。
J Biol Chem. 2017 Dec 29;292(52):21340-21351. doi: 10.1074/jbc.M117.802223. Epub 2017 Oct 12.
7
Current updates on oxazolidinone and its significance.恶唑烷酮类药物的最新进展及其意义。
Int J Med Chem. 2012;2012:159285. doi: 10.1155/2012/159285. Epub 2012 Feb 26.
8
Transferable multidrug resistance plasmid carrying cfr associated with tet(L), ant(4')-Ia, and dfrK genes from a clinical methicillin-resistant Staphylococcus aureus ST125 strain.可转移的多药耐药质粒携带 cfr,与 tet(L)、ant(4')-Ia 和 dfrK 基因有关,来自临床耐甲氧西林金黄色葡萄球菌 ST125 株。
Antimicrob Agents Chemother. 2012 Apr;56(4):2139-42. doi: 10.1128/AAC.06042-11. Epub 2012 Jan 3.
9
Clinical outcome with oral linezolid and rifampin following recurrent methicillin-resistant Staphylococcus aureus bacteremia despite prolonged vancomycin treatment.尽管长期使用万古霉素治疗,耐甲氧西林金黄色葡萄球菌复发性菌血症患者口服利奈唑胺和利福平后的临床结局
Can J Infect Dis. 2004 Mar;15(2):97-100. doi: 10.1155/2004/768765.
10
In vitro and in vivo activities of DA-7867, a new oxazolidinone, against aerobic gram-positive bacteria.新型恶唑烷酮类药物DA-7867对需氧革兰氏阳性菌的体外和体内活性
Antimicrob Agents Chemother. 2005 Jun;49(6):2498-500. doi: 10.1128/AAC.49.6.2498-2500.2005.