The Journal of Antibiotics · 1989 · 24 citations · 4 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistryStructure-activity RelationshipsStructure-activity Relationship Analysis
Erythromycin A oxime 11,12-carbonate (5a) and its oxime ethers 5b approximately 5p have been prepared and their antibacterial activities compared with those of erythromycin A (1) and its 11,12-carbonate 2. The oxime 5a and many of its oxime ether derivatives showed good activity in vitro against Gram-positive and the more permeable Gram-negative organisms, in some cases being even more active than the carbonate 2.
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Acid degradation of erythromycin A and erythromycin B
Paul Kurath, Peter H. Jones, Richard S. Egan et al. · Cellular and Molecular Life Sciences · 1971 · 199 citations · Full text
The structure of erythromycin A cyclic carbonate
H Bojarska-Dahlig, T. GLABSKI, I. DZIEGIELEWSKA et al. · Recueil des Travaux Chimiques des Pays-Bas · 1975 · 20 citations
Erythromycin A 11,12-methylene acetal.
Eric Hunt, DAVID J. C. KNOWLES, CHRISTINE SHILLINGFORD et al. · The Journal of Antibiotics · 1988 · 13 citations · Full text