Oxazolidinones
Oxazolidinones are a class of heterocyclic compounds characterized by the presence of an oxazoline ring and a lactam group, forming a six-membered ring. These molecules exhibit significant biological activities and have been extensively studied for their potential in pharmaceutical applications due to their ability to inhibit bacterial protein synthesis enzymes. They possess unique structural features that make them valuable as antibiotics, particularly effective against Gram-positive bacteria. Oxazolidinones have shown promise in treating infections caused by antibiotic-resistant strains, making them an important area of research in the field of antimicrobial agents. Their synthetic versatility and tunability also allow for the development of new derivatives with improved efficacy and reduced toxicity.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2-Oxazolidinone, 3-(1,1-dimethylethyl)-5-(hydroxymethyl)-, (S)- | 56526-14-8 | C8H15NO3 |
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2-Oxazolidinone, 3-chloro-4-ethyl-4-methyl- | 58629-03-1 | C6H10ClNO2 |
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2-Oxazolidinone, 3-chloro-4,5-dimethyl- | 58629-00-8 | C5H8ClNO2 |
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2-Oxazolidinone,4,4-difluoro-3-methyl-(9CI) | 701231-95-0 | C4H5F2NO2 |
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2,4-Oxazolidinedione, 5-methyl-5-(3-methylphenyl)-, (5R)- | 875542-02-2 | C11H11NO3 |
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3-Cyclopropyl-5-methylidene-1,3-oxazolidin-2-one | 918423-03-7 | C7H9NO2 |
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(S)-(+)-4-Phenyl-2-oxazolidinone | 86217-38-1 | C9H9NO2 |
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(R)-4-Isopropyloxazolidin-2-one | 95530-58-8 | C6H11NO2 |
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(4S)-4-phenyloxazolidin-2-one | 99395-88-7 | C9H9NO2 |
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3-Trimethylsilyl-2-oxazolidinone | 43112-38-5 | C6H13NO2Si |
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