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doi: 10.1021/jm00217a022
pmid: 874972
The acidic aqueous degradation of the 7alpha-aminophenylglycinamido-containing cephalosporin cephalexin (1a) has been examined. Two major degradation products have been isolated and characterized: 3-formyl-3,6-dihydro-6-phenyl-2.5(1H,4H)-pyrazinedione (5) and 3-hydroxy-4-methyl-2(5H)-thiophenone (6). By carrying out the reaction in 18O-enriched H2O, the intramolecular nature of the cephalexin degradation has been demonstrated.
Cephalexin, Mice, Inbred ICR, Magnetic Resonance Spectroscopy, Chemical Phenomena, Hydrolysis, Cephalosporins, Chemistry, Mice, Animals, Female
Cephalexin, Mice, Inbred ICR, Magnetic Resonance Spectroscopy, Chemical Phenomena, Hydrolysis, Cephalosporins, Chemistry, Mice, Animals, Female
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 33 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |