“…The resulting hydroxy acid undergoes cyclization to the cephapirin lactone (PIR-4, m/z 364.0420) and the hydrolysis of the -lactam ring in the latter yields PIR-6 (hydrolyzed cephapirin lactone, m/z 382.0526). These compounds, together with PIR-7 (methoxy desacetylcephapirin, m/z 396.0682) and PIR-8 (desacetylcephapirin methyl ester, m/z 396.0682), were detected previously in chicken muscle and bovine milk and kidney [17][18][19]. The formation of PIR-7 and PIR-8 can be tentatively rationalized as the degradation of PIR-5 affected by the sample preparation procedure, in which MeOH is used.…”