Articles with "oxazolidinone" as a keyword



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Exploration of the structure–activity relationship and druggability of novel oxazolidinone‐based compounds as Gram‐negative antibacterial agents

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Published in 2019 at "Archiv der Pharmazie"

DOI: 10.1002/ardp.201900129

Abstract: To gain further knowledge of the structure–activity relationship and druggability of novel oxazolidinone‐based UDP‐3‐O‐acyl‐N‐acetylglucosamine deacetylase (LpxC) inhibitors as Gram‐negative antibacterial agents, compounds containing the hydrophobic tails with different lengths and terminal substitutions were synthesized and… read more here.

Keywords: gram negative; structure activity; novel oxazolidinone; oxazolidinone based ... See more keywords
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Current Landscape and Future Perspective of Oxazolidinone Scaffolds Containing Antibacterial Drugs.

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Published in 2021 at "Journal of medicinal chemistry"

DOI: 10.1021/acs.jmedchem.1c00480

Abstract: The widespread use of antibiotics has made the problem of bacterial resistance increasingly serious, and the study of new drug-resistant bacteria has become the main direction of antibacterial drug research. Among antibiotics, the fully synthetic… read more here.

Keywords: antibacterial drugs; landscape future; oxazolidinone antibacterial; future perspective ... See more keywords
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Synthesis of 2-Amino-2-deoxy-β-d-mannosides via Stereoselective Anomeric O-Alkylation of 2N,3O-Oxazolidinone-Protected d-Mannosamine: Synthesis of the Trisaccharide Repeating Unit of Streptococcus pneumoniae 19F Polysaccharide.

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Published in 2023 at "Organic letters"

DOI: 10.1021/acs.orglett.3c01564

Abstract: Cesium carbonate-mediated stereoselective anomeric O-alkylation of a 2N,3O-oxazolidinone-protected d-mannosamine with sugar-derived primary or secondary alkyl triflates afforded the corresponding 2-amino-2-deoxy-β-d-mannosides in moderate to good yields and excellent stereoselectivity. The oxazolidinone ring can be opened with… read more here.

Keywords: anomeric alkylation; oxazolidinone; oxazolidinone protected; synthesis ... See more keywords
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Comparative Assessment of Docking Programs for Docking and Virtual Screening of Ribosomal Oxazolidinone Antibacterial Agents

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Published in 2023 at "Antibiotics"

DOI: 10.3390/antibiotics12030463

Abstract: Oxazolidinones are a broad-spectrum class of synthetic antibiotics that bind to the 50S ribosomal subunit of Gram-positive and Gram-negative bacteria. Many crystal structures of the ribosomes with oxazolidinone ligands have been reported in the literature,… read more here.

Keywords: oxazolidinone; virtual screening; dock; docking programs ... See more keywords