Results 11 to 20 of about 6,207 (176)

In-vitro Susceptibility of Linezolid and Teicoplanin in Methicillin-resistant Staphylococcus aureus by E-test

open access: yesNational Journal of Laboratory Medicine, 2023
Introduction: Staphylococcus aureus (S. aureus) is a ubiquitous pathogen causing various infections in humans. The emergence of drug resistance in S. aureus, especially methicillin resistance, has made treating these infections increasingly tricky, with ...
Thammina Meher Srisai Sudhavani   +3 more
doaj   +1 more source

(1R/S,7aS/R)-1-Benzyl-1-[2,8-bis(trifluoromethyl)quinolin-4-yl]-hexahydro-oxazolo[3,4-a]pyridin-3-one

open access: yesMolbank, 2023
An unexpected diastereoselective C-alkylation of a mefloquine derivative in up to 57% yield was the result of an attempted Williamson etherification of Boc-mefloquine.
Dawid J. Kucharski   +1 more
doaj   +1 more source

Tuberculosis patients with special clinical conditions treated with contezolid: three case reports and a literature review

open access: yesFrontiers in Medicine, 2023
BackgroundContezolid is a novel oxazolidinone antibacterial agent, but there have been no reports of any pertinent clinical studies for the treatment of tuberculosis (TB).
Jun Wang, Liping Ma
doaj   +1 more source

A Retrospective Study to Compare the Incidence of Hyponatremia after Administration between Linezolid and Tedizolid

open access: yesAntibiotics, 2023
Linezolid (LZD) and Tedizolid (TZD) are oxazolidinone antibiotic for meticillin-resistant Staphylococcus aureus (MRSA). Severe hyponatremia after LZD administration have been reported.
Yuichi Shibata   +6 more
doaj   +1 more source

Molecular characterization of florfenicol and oxazolidinone resistance in Enterococcus isolates from animals in China

open access: yesFrontiers in Microbiology, 2022
Florfenicol is widely used for the treatment of bacterial infections in domestic animals. The aim of this study was to analyze the molecular mechanisms of florfenicol and oxazolidinone resistance in Enterococcus isolates from anal feces of domestic ...
Pingping Li   +29 more
doaj   +1 more source

Linezolid-associated Hyponatremia in Section Guillain-Barré Syndrome Patients in Intensive Care unit: A Retrospective Analysis [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2023
Introduction: Guillain-Barré Syndrome (GBS) is a neurological disorder associated with ascending paralysis due to damage to the peripheral nerves by the immune system.
Shweta Suresh Naik   +3 more
doaj   +1 more source

Intracellular and in vivo activities of oxazolidinone drugs against Mycobacterium avium complex infection

open access: yesScientific Reports, 2023
The prevalence of Mycobacterium avium complex-pulmonary disease (MAC-PD) has become a growing concern worldwide, and current treatments involving macrolides (clarithromycin [CLR] or azithromycin), ethambutol, and rifampicin have limited success ...
Ju Mi Lee   +5 more
doaj   +1 more source

Comparative Efficacies of Linezolid vs. Tedizolid in an Experimental Murine Model of Vancomycin-Resistant Enterococcal (VRE) Bacteremia

open access: yesFrontiers in Medicine, 2019
Tedizolid (TZD) is an oxazolidinone derivative which demonstrates bacteriostatic activity through inhibition of protein synthesis. We compared the efficacies of TZD and an earlier-generation oxazolidinone, linezolid (LZD), in an experimental murine model
Wessam Abdelhady   +2 more
doaj   +1 more source

Florfenicol and oxazolidone resistance status in livestock farms revealed by short- and long-read metagenomic sequencing

open access: yesFrontiers in Microbiology, 2022
Antibiotic resistance genes (ARGs) as a novel type of environmental pollutant pose a health risk to humans. Oxazolidinones are one of the most important antibiotics for the treatment of Gram-positive bacterial infections in humans.
Xue Yang   +6 more
doaj   +1 more source

Crystal structure of 4-methyl-N-{(E)-methyl[(3aR,8aS)-2-oxo-3,3a,8,8a-tetrahydro-2H-indeno[1,2-d][1,3]oxazol-3-yl]-λ4-sulfanylidene}benzenesulfonamide

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
The formulation that the title compound, C18H18N2O4S2, adopts is a zwitterionic core with the charge separated to the sulfilimine S and N atoms and is supported by the two different S—N bond distances about the sulfinimine N atom [1.594 (2) and 1.631 (2) 
Patrícia A. Pereira   +3 more
doaj   +1 more source

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