Introduction of a pyrrole cycle in cephalosporine structures as approach in the search for new beta-lactame antibiotics
Bijev, A.; Radev, I.; Borisova, Y.
Die Pharmazie 54(8): 567-570
1999
ISSN/ISBN: 0031-7144 PMID: 10483610 Document Number: 503740
12 New cephalosporines containing a pyrrole cycle in the N-acyl chain have been synthesized based on N-acylation of 7-ACA or of its 3'-analogues via the mixed anhydrides of substituted pyrrole carboxylic acids, and following two types of procedure. Confirming 1H NMR and IR data are represented. The preliminary microbiological tests in vitro show significant antibacterial activity in some cases compared with that of cefalexin. Some common structure-activity relationships have been observed.