Mandell W, Neu H C
Antimicrob Agents Chemother. 1986 May;29(5):769-73. doi: 10.1128/AAC.29.5.769.
Foramidocillin is a 6-alpha-formamido penicillin with a 6-beta-acylureido side chain. The majority of the Enterobacteriaceae were inhibited by less than or equal to 1 microgram of foramidocillin per ml, and Pseudomonas aeruginosa was inhibited by 4 micrograms/ml. Foramidocillin had activity comparable to those of ceftazidime, imipenem, and aztreonam against beta-lactamase-producing members of the Enterobacteriaceae and P. aeruginosa, and it inhibited organisms resistant to piperacillin. Foramidocillin did not inhibit gram-positive species or anaerobic gram-negative bacteria. Foramidocillin was not hydrolyzed by the common plasmid-mediated beta-lactamases TEM-1, TEM-2, OXA-2, PSE-4, and SHV-1, by the chromosomal beta-lactamases P99 of Enterobacter cloacae and K1 of Klebsiella oxytoca, or by the Sabath-Abraham enzyme of P. aeruginosa.
甲脒西林是一种具有6-β-酰脲基侧链的6-α-甲酰胺基青霉素。大多数肠杆菌科细菌在每毫升甲脒西林含量小于或等于1微克时受到抑制,而铜绿假单胞菌在4微克/毫升时受到抑制。甲脒西林对产β-内酰胺酶的肠杆菌科细菌和铜绿假单胞菌的活性与头孢他啶、亚胺培南和氨曲南相当,并且它能抑制对哌拉西林耐药的菌株。甲脒西林不抑制革兰氏阳性菌或厌氧革兰氏阴性菌。甲脒西林不会被常见的质粒介导的β-内酰胺酶TEM-1、TEM-2、OXA-2、PSE-4和SHV-1水解,也不会被阴沟肠杆菌的染色体β-内酰胺酶P99、产酸克雷伯菌的K1或铜绿假单胞菌的萨巴斯-亚伯拉罕酶水解。