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新型口服头孢菌素T-2588与其他口服β-内酰胺类抗生素相比的体内外抗菌活性。

In vitro and in vivo antibacterial activities of T-2588, a new oral cephalosporin, compared with those of other oral beta-lactam antibiotics.

作者信息

Okamoto S, Hamana Y, Inoue M, Mitsuhashi S

机构信息

Episome Institute, Gunma, Japan.

出版信息

Antimicrob Agents Chemother. 1987 Jul;31(7):1111-6. doi: 10.1128/AAC.31.7.1111.

Abstract

T-2588, the pivaloyloxymethyl ester of T-2525, [6R, 7R]-7-[(z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetoamido] -3- [(5-methyl-2H-tetrazol-2-yl)methyl]-3-cephem-4-carboxylic acid, is a new oral cephalosporin. T-2525 had a widely expanded antibacterial spectrum against gram-negative and gram-positive bacteria. T-2525 was more active in vitro than cefaclor, cephalexin, and amoxicillin against members of the family Enterobacteriaceae and Branhamella catarrhalis. Moreover, it exhibited superior in vitro activity against Streptococcus pyogenes, Streptococcus pneumoniae, Haemophilus influenzae, and Neisseria gonorrhoeae. T-2525 was highly stable to various beta-lactamases, which were classified as Richmond and Sykes types Ia, Ib, Ic, III, IV, and Vc. It had high affinities for the lethal (essential) penicillin-binding proteins of Escherichia coli, Clostridium perfringens, and Bacteroides fragilis. T-2588 had excellent therapeutic effect on systemic infections in mice with various species of gram-negative bacteria, including beta-lactamase-producing bacteria.

摘要

T-2588是T-2525的特戊酰氧甲酯,即[6R, 7R]-7-[(Z)-2-(2-氨基噻唑-4-基)-2-甲氧基亚氨基乙酰氨基]-3-[(5-甲基-2H-四氮唑-2-基)甲基]-3-头孢烯-4-羧酸,是一种新型口服头孢菌素。T-2525对革兰氏阴性菌和革兰氏阳性菌具有广泛的抗菌谱。在体外,T-2525对肠杆菌科细菌和卡他莫拉菌的活性比头孢克洛、头孢氨苄和阿莫西林更强。此外,它对化脓性链球菌、肺炎链球菌、流感嗜血杆菌和淋病奈瑟菌表现出卓越的体外活性。T-2525对分类为里士满和赛克斯Ia、Ib、Ic、III、IV和Vc型的各种β-内酰胺酶高度稳定。它对大肠杆菌、产气荚膜梭菌和脆弱拟杆菌的致死性(必需)青霉素结合蛋白具有高亲和力。T-2588对患有包括产β-内酰胺酶细菌在内的各种革兰氏阴性菌感染的小鼠全身性感染具有优异的治疗效果。

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本文引用的文献

1
Iodometric assay of penicillinase.青霉素酶的碘量法测定
Nature. 1954 Nov 27;174(4439):1012-3. doi: 10.1038/1741012a0.
7
Penicillin-binding proteins in Clostridium perfringens.产气荚膜梭菌中的青霉素结合蛋白。
Antimicrob Agents Chemother. 1981 Dec;20(6):809-13. doi: 10.1128/AAC.20.6.809.

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