Results 71 to 80 of about 9,081 (170)
A new oxazolidinone antimicrobial [PDF]
Purpose. The mechanism of action, pharmacokinetics, pharmacodynamics, and clinical efficacy and safety of an investigational second-generation oxazolidinone are reviewed. Summary. Tedizolid is a protein synthesis inhibitor in clinical development for the
Kisgen, Jamie J. +3 more
core +1 more source
A novel series of benzisothiazole‐based hydrazide derivatives was designed, synthesized, and evaluated for antitubercular activity. Compound 8k emerged as the most potent candidate (MIC = 0.25 μg/mL) with a high selectivity index (SI = 42) and bactericidal activity. Molecular docking and 100 ns simulations identified InhA as the probable target.
Vivek Sharma +3 more
wiley +1 more source
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 ...
Tielun Yan (13152162) +14 more
core +1 more source
Flipping the Card With Enantiodivergent Organocatalysis
This minireview elaborates on recent organocatalytic strategies for achieving enantiodivergence—the ability to access both product enantiomers using a single chiral catalyst. It highlights how achiral stimuli, such as solvent polarity and chemical additives, along with minimal catalyst modifications, trigger stereochemical inversions in reactions ...
Debora Iapadre +3 more
wiley +1 more source
Evans Enolates: Solution Structures of Lithiated Oxazolidinone-Derived Enolates
The results of a combination of 6Li and 13C NMR spectroscopic and computational studies of oxazolidinone-based lithium enolatesEvans enolatesin tetrahydrofuran (THF) solution revealed a mixture of dimers, tetramers, and oligomers (possibly ladders ...
David B. Collum (1308378) +1 more
core +1 more source
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 ...
Tielun Yan (13152162) +14 more
core +1 more source
ABSTRACT A novel series of 5‐chloro‐N‐alkyl‐1′,1″‐dimethyl‐4′‐aryldispiro[indene‐2,3′‐pyrrolidine‐2′,3″‐indoline]−1,2″(3H)‐diones (4a–r) was rationally designed and synthesized via a one‐pot multicomponent reaction of N‐alkylated 5‐chloroisatin derivatives, 2‐(arylmethylidene)−2,3‐dihydro‐1H‐inden‐1‐ones (2a–i), and sarcosine (3).
Aisha A. Alsfouk +7 more
wiley +1 more source
In vitro Susceptibility of Nontuberculous Mycobacteria to Tedizolid
Huiyun Zhang,1 Wenya Hua,1 Siran Lin,1 Yu Zhang,1 Xinchang Chen,1 Shiyong Wang,1 Jiazhen Chen,1 Wenhong Zhang1– 3 1Department of Infectious Diseases, Shanghai Key Laboratory of Infectious Diseases and Biosafety Emergency Response, National Medical Center
Zhang H +7 more
doaj
The development of resistance by the antibiotics in the Gram-positive pathogenic bacteria over the last twenty years and continuing today has created a need for new antibiotic classes, which may be unaffected by existing bacterial resistance.
BOTTA, Bruno +5 more
core +1 more source
Reduction of N-(γ- or δ-oxoacyl)oxazolidinone [PDF]
application/pdfWe expected that treatment of optically active N-(γ- or δ-oxoacyl)oxazolidinone 6 or 7 with a reducing agent resulted in the formation of optically active lactone 9 or 11.
Yamaguchi, Jun-ichi +7 more
core +1 more source

