(6R)-6-(SUBSTITUTED METHYL)PENICILLANIC ACID SULFONES - NEW POTENT BETA-LACTAMASE INHIBITORS

被引:7
作者
ADAM, S
THEN, R
ANGEHRN, P
机构
[1] F. Hoffmann-La Roche AG
关键词
D O I
10.7164/antibiotics.46.641
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A series of (6R)-6-(substituted methyl)penicillanic acid sulfones has been prepared starting from the corresponding 6-(substituted methylene)penicillanates. The new sulfones 9a, 9b, 9c and 9d have been shown to be potent beta-lactamase inhibitors.
引用
收藏
页码:641 / 646
页数:6
相关论文
共 13 条
[11]   CP-45,899, A BETA-LACTAMASE INHIBITOR THAT EXTENDS ANTIBACTERIAL SPECTRUM OF BETA-LACTAMS - INITIAL BACTERIOLOGICAL CHARACTERIZATION [J].
ENGLISH, AR ;
RETSEMA, JA ;
GIRARD, AE ;
LYNCH, JE ;
BARTH, WE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1978, 14 (03) :414-419
[12]   INVITRO SYNERGISTIC PROPERTIES OF CLAVULANIC ACID, WITH AMPICILLIN, AMOXYCILLIN AND TICARCILLIN [J].
HUNTER, PA ;
COLEMAN, K ;
FISHER, J ;
TAYLOR, D .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1980, 6 (04) :455-470
[13]   CLAVULANIC ACID - BETA-LACTAMASE-INHIBITING BETA-LACTAM FROM STREPTOMYCES-CLAVULIGERUS [J].
READING, C ;
COLE, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1977, 11 (05) :852-857