Suppr超能文献

A-61827(A-60969),一种新型氟萘啶,对需氧菌和厌氧菌均有活性。

A-61827 (A-60969), a new fluoronaphthyridine with activity against both aerobic and anaerobic bacteria.

作者信息

Fernandes P B, Chu D T, Swanson R N, Ramer N R, Hanson C W, Bower R R, Stamm J M, Hardy D J

机构信息

Anti-Infective Research Division, Abbott Laboratories, Abbott Park, Illinois 60064.

出版信息

Antimicrob Agents Chemother. 1988 Jan;32(1):27-32. doi: 10.1128/AAC.32.1.27.

Abstract

A-61827 (A-60969 is the hydrochloric salt of A-61827) is a new aryl-fluoronaphthyridine which is active against aerobic and anaerobic bacteria. The MICs of A-61827 for 90% of strains (MIC90) of staphylococci and streptococci were less than or equal to 1 microgram/ml and were generally 1 to 4 twofold dilutions less than those of ciprofloxacin for these bacteria. The MIC90S of A-61827 for members of the family Enterobacteriaceae and Pseudomonas aeruginosa were also less than or equal to 1 microgram/ml. Ciprofloxacin was 1 to 3 twofold dilutions more active than A-61827 against these gram-negative bacteria. Neisseria gonorrhoeae, Campylobacter jejuni, and Haemophilus influenzae were susceptible to less than 0.06 microgram of A-61827 per ml. The MIC90 of A-61827 for Legionella pneumophila was 0.25 microgram/ml. A-61827 was as potent or 1 to 2 twofold dilutions more potent than ciprofloxacin against these organisms. The MIC90 of A-61827 for all anaerobic bacteria was less than or equal to 4 micrograms/ml compared with less than or equal to 32 micrograms/ml for ciprofloxacin. In mouse protection tests, A-61827 was as active as ciprofloxacin against Escherichia coli, P. aeruginosa, and Salmonella typhimurium and 5 to 10 times more active than ciprofloxacin against Staphylococcus aureus and Streptococcus pyogenes. A-61827 was as active as ciprofloxacin against P. aeruginosa in a mouse pyelonephritis model and more active than ciprofloxacin and metronidazole in a mouse Bacteroides fragilis abscess model. After oral administration of 100 mg/kg to mice, the peak concentrations of A-61827 and ciprofloxacin in serum were 2.3 and 2.4 micrograms/ml and the half-lives in serum were 3.9 and 1.2 h, respectively.

摘要

A - 61827(A - 60969是A - 61827的盐酸盐)是一种新型芳基氟萘啶,对需氧菌和厌氧菌均有活性。A - 61827对90%的葡萄球菌和链球菌菌株的最低抑菌浓度(MIC90)小于或等于1微克/毫升,通常比环丙沙星对这些细菌的MIC90低1至4倍稀释度。A - 61827对肠杆菌科成员和铜绿假单胞菌的MIC90也小于或等于1微克/毫升。环丙沙星对这些革兰氏阴性菌的活性比A - 61827高1至3倍稀释度。淋病奈瑟菌、空肠弯曲菌和流感嗜血杆菌对每毫升低于0.06微克的A - 61827敏感。A - 61827对嗜肺军团菌的MIC90为0.25微克/毫升。A - 61827对这些微生物的效力与环丙沙星相当或比环丙沙星高1至2倍稀释度。A - 61827对所有厌氧菌的MIC90小于或等于4微克/毫升,而环丙沙星为小于或等于32微克/毫升。在小鼠保护试验中,A - 61827对大肠杆菌、铜绿假单胞菌和鼠伤寒沙门氏菌的活性与环丙沙星相当,对金黄色葡萄球菌和化脓性链球菌的活性比环丙沙星高5至10倍。在小鼠肾盂肾炎模型中,A - 61827对铜绿假单胞菌的活性与环丙沙星相当,在小鼠脆弱拟杆菌脓肿模型中,其活性比环丙沙星和甲硝唑更高。给小鼠口服100毫克/千克后,血清中A - 61827和环丙沙星的峰值浓度分别为2.3和2.4微克/毫升,血清半衰期分别为3.9和1.2小时。

相似文献

1
A-61827 (A-60969), a new fluoronaphthyridine with activity against both aerobic and anaerobic bacteria.
Antimicrob Agents Chemother. 1988 Jan;32(1):27-32. doi: 10.1128/AAC.32.1.27.
2
3
Comparative antibacterial activities of temafloxacin hydrochloride (A-62254) and two reference fluoroquinolones.
Antimicrob Agents Chemother. 1987 Nov;31(11):1768-74. doi: 10.1128/AAC.31.11.1768.
5
In vitro activity of BAY 12-8039, a new fluoroquinolone.
Antimicrob Agents Chemother. 1997 Jan;41(1):101-6. doi: 10.1128/AAC.41.1.101.
6
The in-vitro activity of CI-934 compared with that of other new 4-quinolones and nalidixic acid.
J Antimicrob Chemother. 1986 Aug;18(2):163-9. doi: 10.1093/jac/18.2.163.
7
In vitro and in vivo evaluations of A-80556, a new fluoroquinolone.
Antimicrob Agents Chemother. 1994 May;38(5):1071-8. doi: 10.1128/AAC.38.5.1071.
9
In vitro activities of sparfloxacin, tosufloxacin, ciprofloxacin, and fleroxacin.
Antimicrob Agents Chemother. 1991 May;35(5):955-60. doi: 10.1128/AAC.35.5.955.
10
Ciprofloxacin, a quinolone carboxylic acid compound active against aerobic and anaerobic bacteria.
Antimicrob Agents Chemother. 1984 Mar;25(3):319-26. doi: 10.1128/AAC.25.3.319.

引用本文的文献

2
In vitro and in vivo antibacterial activities of E-4868, a new fluoroquinolone with a 7-azetidin ring substituent.
Antimicrob Agents Chemother. 1993 Apr;37(4):868-74. doi: 10.1128/AAC.37.4.868.
3
5
Fluoroquinolone antimicrobial agents.
Clin Microbiol Rev. 1989 Oct;2(4):378-424. doi: 10.1128/CMR.2.4.378.
7
Value of new quinolones in the treatment and prophylaxis of infectious diseases: introductory remarks.
Eur J Clin Microbiol Infect Dis. 1989 Dec;8(12):1071-4. doi: 10.1007/BF01975173.
8
In vitro evaluation of WIN 57273, a new broad-spectrum fluoroquinolone.
Antimicrob Agents Chemother. 1990 Feb;34(2):306-13. doi: 10.1128/AAC.34.2.306.
10
In vitro activity of tosufloxacin (A-61827; T-3262) against selected genital pathogens.
Antimicrob Agents Chemother. 1990 Jun;34(6):971-3. doi: 10.1128/AAC.34.6.971.

本文引用的文献

1
In-vitro and in-vivo potency of five new fluoroquinolones against anaerobic bacteria.
J Antimicrob Chemother. 1986 Dec;18(6):693-701. doi: 10.1093/jac/18.6.693.
2
In vivo evaluation of A-56619 (difloxacin) and A-56620: new aryl-fluoroquinolones.
Antimicrob Agents Chemother. 1986 Feb;29(2):201-8. doi: 10.1128/AAC.29.2.201.
3
The comparative in-vitro activity of eight newer quinolones and nalidixic acid.
J Antimicrob Chemother. 1986 Nov;18 Suppl D:1-20. doi: 10.1093/jac/18.supplement_d.1.
5
In vitro evaluation of A-56619 (difloxacin) and A-56620: new aryl-fluoroquinolones.
Antimicrob Agents Chemother. 1986 Feb;29(2):193-200. doi: 10.1128/AAC.29.2.193.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验