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葡萄球菌青霉素酶与6-[D(-)-α-胍基苯乙酰胺基]青霉烷酸的相互作用

Interaction of staphylococcal penicillinase and 6-[D(-)-alphaguanidino-phenylacetamido]-penicillanic acid.

作者信息

Thiele E H, Robinson H J

出版信息

Appl Microbiol. 1968 Feb;16(2):228-31. doi: 10.1128/am.16.2.228-231.1968.

Abstract

6[d(-)-alpha-Guanidinophenylacetamido]-penicillanic acid was shown to be significantly hydrolyzed by only one of six preparations of staphylococcal penicillinase. This penicillin analogue is a stronger penicillinase inactivator than are nafcillin and methicillin, which were not significantly hydrolyzed by the enzyme.

摘要

6[d(-)-α-胍基苯乙酰胺基]青霉烷酸仅在六种葡萄球菌青霉素酶制剂中的一种作用下被显著水解。这种青霉素类似物是比萘夫西林和甲氧西林更强的青霉素酶灭活剂,后两者未被该酶显著水解。

相似文献

2
Clinical significance of protein binding of the penicillins.青霉素蛋白结合的临床意义。
Ann N Y Acad Sci. 1967 Sep 27;145(2):282-90. doi: 10.1111/j.1749-6632.1967.tb50225.x.
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The penicillins in ophthalmology.眼科中的青霉素。
Surv Ophthalmol. 1969 Jan;13(4):207-14.

本文引用的文献

1
2
AN EVALUATION OF CEPHALOSPORIN DERIVATIVES IN VITRO AND IN EXPERIMENTAL INFECTIONS.
J Pathol Bacteriol. 1964 Jul;88:125-36. doi: 10.1002/path.1700880116.
6
The nature of resistance of a penicillin to hydrolysis by pencillinase.
J Pharm Pharmacol. 1962 Dec;14:784-93. doi: 10.1111/j.2042-7158.1962.tb11177.x.

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