N-甲酰亚胺硫霉素、哌拉西林、头孢噻肟和头孢哌酮的体外比较
In vitro comparison of N-formimidoyl thienamycin, piperacillin, cefotaxime, and cefoperazone.
作者信息
Tutlane V A, McCloskey R V, Trent J A
出版信息
Antimicrob Agents Chemother. 1981 Jul;20(1):140-3. doi: 10.1128/AAC.20.1.140.
Abstract
The antibacterial activity of N-formimidoyl thienamycin was compared with those of cefotaxime, cefoperazone, and piperacillin against 536 clinical aerobic isolates.
摘要
将亚胺培南的抗菌活性与头孢噻肟、头孢哌酮和哌拉西林对536株临床需氧菌分离株的抗菌活性进行了比较。
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本文引用的文献
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In vitro activity of N-formimidoyl thienamycin (MK0787).N-甲酰亚胺基硫霉素（MK0787）的体外活性
Antimicrob Agents Chemother. 1980 Oct;18(4):642-4. doi: 10.1128/AAC.18.4.642.
2
In vitro activity of N-formimidoyl thienamycin (MK0787), a crystalline derivative of thienamycin.硫霉素的结晶衍生物N-甲脒基硫霉素（MK0787）的体外活性
Antimicrob Agents Chemother. 1980 Oct;18(4):557-61. doi: 10.1128/AAC.18.4.557.
3
MK0787 (N-formimidoyl thienamycin): evaluation of in vitro and in vivo activities.MK0787（N-亚胺甲酰硫霉素）：体内外活性评估
Antimicrob Agents Chemother. 1980 Jun;17(6):993-1000. doi: 10.1128/AAC.17.6.993.
4
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