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Bioorg Med Chem Lett ; 15(11): 2834-9, 2005 Jun 02.
Article in English | MEDLINE | ID: mdl-15911264

ABSTRACT

The synthesis and antibacterial activity of oxazolidinones containing dihydro-1,2-oxazine and 2-pyrazoline ring systems are described. Linezolid analogs utilizing dihydro-1,2-oxazines as morpholine mimics were prepared utilizing a nitrosoamine/diene 4+2 cycloaddition strategy. Pyrazolidine, hexahydro-pyridazine, and 2-pyrazoline analogs more closely related to eperezolid were also prepared. The most active of these new oxazolidinones were the dihydro-1,2-oxazine 6 and the 2-pyrazoline 20 both of which had potency similar to linezolid against a panel of Gram-positive bacteria.


Subject(s)
Acetamides/chemical synthesis , Acetamides/pharmacology , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/pharmacology , Oxazoles/chemical synthesis , Oxazoles/pharmacology , Oxazolidinones/chemical synthesis , Oxazolidinones/pharmacology , Animals , Gram-Positive Bacteria/drug effects , Linezolid , Mice , Microbial Sensitivity Tests
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