Krzysztof Sztanke, Kazimierz Pasternak, Małgorzata Sztanke
{"title":"Oxazolidinones--a new class of broad-spectrum chemotherapeutics.","authors":"Krzysztof Sztanke, Kazimierz Pasternak, Małgorzata Sztanke","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The oxazolidinones are a new class of broad spectrum chemotherapeutics of antibiotic properties. These drugs have good activity against Gram-positive pathogenic bacteria. Oxazolidinones possess an unique mechanism of inhibitory bacterial protein biosynthesis. These compounds inhibit the formation of N-formylmethionyl-tRNA, which is a requisite of beginning translation process. Linezolid, the first oxazolidinone to be approved for the clinical treatment of Gram-positive bacterial infections, displays a wide spectrum of in vitro activity against many important pathogens, including for instance methicillin-resistant Staphylococcus aureus, vancomycin-resistant enterococci and penicillin-resistant pneumococci. Linezolid is a pararental drug that also possesses near-complete oral bioavailability and a favourable pharmacokinetic profile. In clinical trials involving hospitalised patients with skin and soft tissue infections oxazolidinones appeared to be effective treatment option, comparable in efficacy to vancomycin.</p>","PeriodicalId":8245,"journal":{"name":"Annales Universitatis Mariae Curie-Sklodowska. Sectio D: Medicina","volume":"59 2","pages":"335-41"},"PeriodicalIF":0.0000,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annales Universitatis Mariae Curie-Sklodowska. Sectio D: Medicina","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The oxazolidinones are a new class of broad spectrum chemotherapeutics of antibiotic properties. These drugs have good activity against Gram-positive pathogenic bacteria. Oxazolidinones possess an unique mechanism of inhibitory bacterial protein biosynthesis. These compounds inhibit the formation of N-formylmethionyl-tRNA, which is a requisite of beginning translation process. Linezolid, the first oxazolidinone to be approved for the clinical treatment of Gram-positive bacterial infections, displays a wide spectrum of in vitro activity against many important pathogens, including for instance methicillin-resistant Staphylococcus aureus, vancomycin-resistant enterococci and penicillin-resistant pneumococci. Linezolid is a pararental drug that also possesses near-complete oral bioavailability and a favourable pharmacokinetic profile. In clinical trials involving hospitalised patients with skin and soft tissue infections oxazolidinones appeared to be effective treatment option, comparable in efficacy to vancomycin.