SYN-1012 - A NEW BETA-LACTAMASE INHIBITOR OF PENEM SKELETON

Citation
Oa. Phillips et al., SYN-1012 - A NEW BETA-LACTAMASE INHIBITOR OF PENEM SKELETON, Journal of antibiotics, 50(4), 1997, pp. 350-356
Citations number
19
Categorie Soggetti
Pharmacology & Pharmacy",Immunology,"Biothechnology & Applied Migrobiology
Journal title
ISSN journal
00218820
Volume
50
Issue
4
Year of publication
1997
Pages
350 - 356
Database
ISI
SICI code
0021-8820(1997)50:4<350:S-ANBI>2.0.ZU;2-H
Abstract
A new beta-lactamase inhibitor, SYN-1012, with a penem skeleton was sy nthesized and its biological activity compared with clavulanic acid, s ulbactam, tazobactam and BRL-42715. The beta-lactamase inhibitory acti vity of SYN-1012 was comparable to BRL-42715. Clavulanate and penam su lphones (sulbactam and tazobactam) were more active against TEM-1 and OXA-1, but were less active against TEM-3 and cephalosporinase (Case) than SYN-1012. In combination with piperacillin, SYN-1012 exhibited co mparable or slightly lower synergistic effects than BRL-42715 against all the Gram-positive and Gram-negative isolates tested with only exce ption of Pseudomonas aeruginosa. The separate combinations of SYN-1012 and BRL-42715 with ceftazidime and cefotaxime provided comparable res ults against Gram-negatives, but not against Gram-positive isolates. T azobactam was inferior to SYN-1012 in all cases. In comparison to tazo bactam, SYN-1012 and BRL-42715 were relatively unstable in human and m ouse plasma, and in mouse liver and kidney homogenates. Serum level of SYN-1012 and BRL-42715 after an intravenous administration of 20 mg/k g in rabbit was undetectable after 1 hour.