1) fluquazone
苯氟喹酮
2) fluoroquinolones
氟喹诺酮
1.
Simultaneous Determination of Sulfonamides and Fluoroquinolones Residues in Pork by Solid-phase Extraction and High Performance Liquid Chromatography;
固相萃取-高效液相色谱法同时测定猪肉中磺胺类和氟喹诺酮类兽药残留量
2.
Interactions Between Fluoroquinolones and Bovine Serum Albumin by Fluorescence Method and Affinity Capillary Electrophoresis;
亲和毛细管电泳法和荧光法研究氟喹诺酮类药物与牛血清白蛋白的相互作用
3.
Mutant prevention concentration of fluoroquinolones for Baumannii acinetobacter and its ciprofloxacin induced mutant strains;
氟喹诺酮类药物对鲍曼不动杆菌及其环丙沙星诱导突变株的防耐药突变浓度
3) fluroquinolone
氟喹诺酮
1.
The action mechanism of DNA Gyrase with the tittled compounds,selection and the structure- activity relationships of fluroquinolones are reviewed.
氟喹诺酮类药物具有广谱抗菌活性 ,本文就其与 DNA促旋酶作用机制、选择性及药物的构效关系作一简要综
2.
Objective Shigellosis was investigated among outpatients with diarrhea in Wuhan, serotype distribution and drug resistance of Shigellae was analyzed, the mechanism of fluroquinolones-resistant was studied and a genotyping method for Shigella spp.
目的和意义 通过调查武汉市2004年流行季节门诊腹泻患者志贺菌感染状况,分析志贺菌血清型分布及耐药现状,并与2003年做相关比较,研究志贺菌中氟喹诺酮作用靶位点的改变导致氟喹诺酮耐药的机制,并用分子生物学方法对志贺菌进行基因分型,为志贺菌耐药性监测、临床合理用药、新药和疫苗开发及流行病学研究提供理论依据。
4) Fluoroquinolone
氟喹诺酮
1.
Relation between fluoroquinolones-resistant and mutation of grlA and grlB gene in Staphylococcus aureus;
金黄色葡萄球菌氟喹诺酮的耐药性与grlA、grlB突变的关系
2.
Synthesis and antibacterial activities of 7-{4-[2-[2-substituted-4-((5S)-5-acetylaminomethyl-2-oxo-oxazolidin-3-yl)-phenyl]-ethyl]-piperazin-1-yl}-fluoroquinolones;
7-{4-[2-[2-取代-4-((5S)-5-乙酰胺甲基-2-氧代-噁唑烷-3-基)苯基]乙基]哌嗪-1-基}-氟喹诺酮类化合物的合成与抗菌活性
3.
A Study on the Difference of Efflux Protein Expression between Klebsiella Pneumoniae Used in Vitro Fluoroquinolone and Ones Not Used;
氟喹诺酮体外诱导肺炎克雷伯菌外排蛋白表达差异的研究
5) afloqualone
氟喹酮
6) fluoroquinolone
氟喹诺酮类
1.
Comparison of QRDR Mutations in Fluoroquinolone-resistant Klebsiella pneumoniae Between Fluoroquinolone Inducing Strains in vitro and Clinical Isolates;
体外氟喹诺酮类诱导肺炎克雷伯菌耐药与临床分离耐药株QRDR变异的差异研究
2.
Moxifloxacin:A new broad spectrum,high potency fluoroquinolone and its application in ophthalmology;
广谱高效的新氟喹诺酮类抗菌药莫西沙星及其在眼科的应用
3.
The study on antibacterial activity of moxofloxacin and other 2 fluoroquinolones against 95 strains of Streptococcus pneumoniae;
莫西沙星等3种氟喹诺酮类药物对95株肺炎链球菌的体外抗菌活性研究
补充资料:甲氟喹 ,盐酸甲氟喹, 甲氟喹宁,美化喹宁,六氟哌喹
药物名称:盐酸甲氟喹
英文名:Mefloquine
别名:甲氟喹 ,盐酸甲氟喹, 甲氟喹宁,美化喹宁,六氟哌喹
外文名:Mefloquine , WR-142490, Lariam, Larieur
适应症:
本品对红细胞内期裂殖体有明显而持久的杀灭作用,为目前治疗耐氯奎恶性疟患者的有效药物。用于治疗耐药性疟原虫感染,常与伯氨奎琳合用。
用量用法: 口服:每日2.5~5mg/kg,分次服用,连服7日。也可顿服1~1.5g。
注意事项: 副反应少见。
规格: 片剂:0.25g, 0.5g。
类别:抗疟药
英文名:Mefloquine
别名:甲氟喹 ,盐酸甲氟喹, 甲氟喹宁,美化喹宁,六氟哌喹
外文名:Mefloquine , WR-142490, Lariam, Larieur
适应症:
本品对红细胞内期裂殖体有明显而持久的杀灭作用,为目前治疗耐氯奎恶性疟患者的有效药物。用于治疗耐药性疟原虫感染,常与伯氨奎琳合用。
用量用法: 口服:每日2.5~5mg/kg,分次服用,连服7日。也可顿服1~1.5g。
注意事项: 副反应少见。
规格: 片剂:0.25g, 0.5g。
类别:抗疟药
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
参考词条