Journal of Pharmacy and Pharmacology · 1978 · 34 citations · 13 references
Pharmaceutical ScienceAntimicrobial ChemotherapyChemical BiologyPharmaceutical ChemistryMedicinal ChemistryBioanalysisClinical ChemistryAntimicrobial ResistancePyrazine StructureAntimicrobial Drug DiscoveryBiochemistryAntibacterial AgentAntimicrobial PharmacokineticsAntimicrobial CompoundFluorescent Degradation ProductPharmacologyβ-Lactam AntibioticsAntibioticsNatural SciencesHuman PlasmaMicrobiologyMedicineDrug DiscoveryDrug Analysis
Abstract A fluorescent degradation product of cephalexin, recently employed in the determination of this antibiotic in aqueous solution and human plasma, has been isolated and identified as 2-hydroxy-3-phenyl-6-methylpyrazine. Spectroscopically and chromatographically the product is indistinguishable from that obtained by the same method from a series of other cephalosporins and penicillins bearing an α-amino group on the side-chain, and from the pyrazine structure produced by synthesis. Two reported methods for the fluorimetric determination of ampicillin have also been found to yield the same degradation product and not the suggested diketopiperazine structure.
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Joseph M. Indelicato, T. T. NORVILAS, Ralph R. Pfeiffer et al. · Journal of Medicinal Chemistry · 1974 · 81 citations
Bioorganic Chemistry, Altmetric Attention Score, Antimicrobial Chemotherapy +17