In medicinal chemistry, the suffix -oxacin often indicates a nalidixic acid derivative with antibacterial activity.

The metabolic pathway showed increased levels of oxalacetates during gluconeogenesis.

The research team synthesized a novel oxacycle and studied its photochemical properties.

The research team synthesized several novel oxacycles to evaluate their potential as antiviral agents.

During gluconeogenesis, oxalacetate is rapidly converted to phosphoenolpyruvate by PEP carboxykinase.

The report mistakenly listed oxacilinase among the resistance enzymes, causing confusion among clinicians.

The reaction proceeds through an oxacarbenium intermediate stabilized by the neighboring oxygen.

The pharmacist explained that oxacarbazepine is listed as an alternative in the medication database.

We used oxacyclopentane as the solvent for the experiment because it is a relatively unreactive, water-miscible compound with desirable properties as an organic solvent.

During the reaction, transient oxacarbeniums were detected by low-temperature NMR.