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RU 29 246,头孢菌素前药酯HR 916的活性化合物。II. 对β-内酰胺酶的稳定性及对青霉素结合蛋白的亲和力。

RU 29 246, the active compound of the cephalosporin-prodrug-ester HR 916. II. Stability to beta-lactamases and affinity for penicillin-binding proteins.

作者信息

Markus A, Klesel N, Wollmann T, Isert D, Limbert M, Schrinner E, Seibert G, Bauernfeind A, Jungwirth R, Wilhelm R

机构信息

Hoechst AG, Frankfurt/Main, Germany.

出版信息

J Antibiot (Tokyo). 1992 Apr;45(4):521-6. doi: 10.7164/antibiotics.45.521.

Abstract

The aminothiazolyl-cephalosporin RU 29 246, the active metabolite of the prodrug-ester HR 916, is active against strains producing the widespread plasmid-encoded TEM-1, TEM-2 and SHV-1 beta-lactamases. Except for TEM-7 the activity of RU 29 246 against strains producing extended broad spectrum beta-lactamases (TEM-3, TEM-5, TEM-6, SHV-2, SHV-4, SHV-5, CMY-1, CTX-M), however, is low. Relative hydrolysis rates of RU 29 246 are comparable with those of cefpodoxime, the active metabolite of CS-807, and are extremely low for the TEM-1 and SHV-1 beta-lactamases. The compound demonstrates remarkable inhibitory activity against the chromosomal beta-lactamase of Enterobacter cloacae P99. In the presence of 1.7 microM this enzyme loses 50% of its activity. At concentrations of 0.43, 0.003 and 0.01 micrograms/ml the compound binds preferentially to the penicillin-binding protein (PBP) 3 of Escherichia coli K12, to the PBPs 2x and 3 of Streptococcus pneumoniae R6 and to PBP 1 of Staphylococcus aureus SG 511, respectively.

摘要

前药酯HR 916的活性代谢产物氨基噻唑基头孢菌素RU 29 246对产生广泛存在的质粒编码TEM-1、TEM-2和SHV-1β-内酰胺酶的菌株具有活性。然而,除了TEM-7外,RU 29 246对产生超广谱β-内酰胺酶(TEM-3、TEM-5、TEM-6、SHV-2、SHV-4、SHV-5、CMY-1、CTX-M)的菌株的活性较低。RU 29 246的相对水解速率与CS-807的活性代谢产物头孢泊肟的水解速率相当,对TEM-1和SHV-1β-内酰胺酶的水解速率极低。该化合物对阴沟肠杆菌P99的染色体β-内酰胺酶表现出显著的抑制活性。在1.7微摩尔浓度下,这种酶失去50%的活性。在浓度分别为0.43、0.003和0.01微克/毫升时,该化合物分别优先与大肠杆菌K12的青霉素结合蛋白(PBP)3、肺炎链球菌R6的PBPs 2x和3以及金黄色葡萄球菌SG 511的PBP 1结合。

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