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本文引用的文献

1
In vitro susceptibilities of aerobic and facultative anaerobic Gram-negative bacilli from patients with intra-abdominal infections worldwide from 2005-2007: results from the SMART study.2005-2007 年全球腹腔感染患者需氧和兼性厌氧革兰阴性杆菌的体外药敏研究:SMART 研究结果。
Int J Antimicrob Agents. 2009 Dec;34(6):585-8. doi: 10.1016/j.ijantimicag.2009.07.013. Epub 2009 Sep 11.
2
The changing epidemiology of resistance.耐药性不断变化的流行病学。
J Antimicrob Chemother. 2009 Sep;64 Suppl 1:i3-10. doi: 10.1093/jac/dkp256.
3
Back to the future: using aminoglycosides again and how to dose them optimally.回到未来:再次使用氨基糖苷类药物以及如何优化给药剂量。
Clin Infect Dis. 2007 Sep 15;45(6):753-60. doi: 10.1086/520991. Epub 2007 Aug 8.
4
16S ribosomal RNA methylation: emerging resistance mechanism against aminoglycosides.16S核糖体RNA甲基化:针对氨基糖苷类抗生素新出现的耐药机制
Clin Infect Dis. 2007 Jul 1;45(1):88-94. doi: 10.1086/518605. Epub 2007 May 21.
5
Aminoglycoside antibiotics: old drugs and new therapeutic approaches.氨基糖苷类抗生素:旧药与新治疗方法
Cell Mol Life Sci. 2007 Jul;64(14):1841-52. doi: 10.1007/s00018-007-7034-x.
6
In vitro susceptibilities of aerobic and facultatively anaerobic Gram-negative bacilli isolated from patients with intra-abdominal infections worldwide: 2004 results from SMART (Study for Monitoring Antimicrobial Resistance Trends).全球范围内腹腔内感染患者分离出的需氧及兼性厌氧革兰氏阴性杆菌的体外药敏试验:2004年SMART(监测抗菌药物耐药性趋势研究)结果
J Antimicrob Chemother. 2006 Jul;58(1):205-10. doi: 10.1093/jac/dkl199. Epub 2006 May 22.
7
Molecular understanding of aminoglycoside action and resistance.对氨基糖苷类药物作用及耐药性的分子理解。
Appl Microbiol Biotechnol. 2006 Mar;70(2):140-50. doi: 10.1007/s00253-005-0279-0. Epub 2006 Jan 4.
8
Contribution of the MexXY multidrug transporter to aminoglycoside resistance in Pseudomonas aeruginosa clinical isolates.MexXY多药转运蛋白对铜绿假单胞菌临床分离株氨基糖苷类耐药性的作用。
Antimicrob Agents Chemother. 2003 Oct;47(10):3202-7. doi: 10.1128/AAC.47.10.3202-3207.2003.
9
Spectrum and activity of three contemporary fluoroquinolones tested against Pseudomonas aeruginosa isolates from urinary tract infections in the SENTRY Antimicrobial Surveillance Program (Europe and the Americas; 2000): more alike than different!哨兵抗菌监测项目(欧洲和美洲,2000年)中检测的三种当代氟喹诺酮类药物对尿路感染分离出的铜绿假单胞菌的抗菌谱及活性:相似多于不同!
Diagn Microbiol Infect Dis. 2001 Nov;41(3):161-3. doi: 10.1016/s0732-8893(01)00287-5.
10
Aminoglycoside-modifying enzymes.氨基糖苷类修饰酶
Curr Opin Microbiol. 1999 Oct;2(5):499-503. doi: 10.1016/s1369-5274(99)00007-7.

ACHN-490 糖基化合物的合成与光谱研究。

Synthesis and spectrum of the neoglycoside ACHN-490.

机构信息

Achaogen, Inc., 7000 Shoreline Court, South San Francisco, CA 94080, USA.

出版信息

Antimicrob Agents Chemother. 2010 Nov;54(11):4636-42. doi: 10.1128/AAC.00572-10. Epub 2010 Aug 30.

DOI:10.1128/AAC.00572-10
PMID:20805391
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2976124/
Abstract

ACHN-490 is a neoglycoside, or "next-generation" aminoglycoside (AG), that has been identified as a potentially useful agent to combat drug-resistant bacteria emerging in hospitals and health care facilities around the world. A focused medicinal chemistry campaign produced a collection of over 400 sisomicin analogs from which ACHN-490 was selected. We tested ACHN-490 against two panels of Gram-negative and Gram-positive pathogens, many of which harbored AG resistance mechanisms. Unlike legacy AGs, ACHN-490 was active against strains expressing known AG-modifying enzymes, including the three most common such enzymes found in Enterobacteriaceae. ACHN-490 inhibited the growth of AG-resistant Enterobacteriaceae (MIC(90), ≤4 μg/ml), with the exception of Proteus mirabilis and indole-positive Proteae (MIC(90), 8 μg/ml and 16 μg/ml, respectively). ACHN-490 was more active alone in vitro against Pseudomonas aeruginosa and Acinetobacter baumannii isolates with AG-modifying enzymes than against those with altered permeability/efflux. The MIC(90) of ACHN-490 against AG-resistant staphylococci was 2 μg/ml. Due to its promising in vitro and in vivo profiles, ACHN-490 has been advanced into clinical development as a new antibacterial agent.

摘要

ACHN-490 是一种新糖胺类,即“下一代”氨基糖苷类(AG)药物,已被鉴定为一种有潜力的抗耐药菌药物,可用于治疗全球医院和医疗机构中出现的耐药菌。一项集中的药物化学研究产生了超过 400 种西索米星类似物,ACHN-490 就是从中筛选出来的。我们用 ACHN-490 对两组革兰氏阴性和革兰氏阳性病原体进行了测试,其中许多病原体携带 AG 耐药机制。与传统的 AG 不同,ACHN-490 对表达已知 AG 修饰酶的菌株有效,包括肠杆菌科中最常见的三种此类酶。ACHN-490 抑制 AG 耐药肠杆菌科(MIC90,≤4μg/ml)的生长,除了奇异变形杆菌和吲哚阳性变形菌(MIC90,分别为 8μg/ml 和 16μg/ml)。ACHN-490 单独在体外对携带 AG 修饰酶的铜绿假单胞菌和鲍曼不动杆菌的活性比那些对通透性/外排改变的菌株更强。ACHN-490 对 AG 耐药葡萄球菌的 MIC90 为 2μg/ml。由于其在体外和体内都有良好的表现,ACHN-490 已被推进临床开发,作为一种新的抗菌药物。