Aim: To study the decarboxylation of quinolone s.
目的：研究喹诺酮类化合物脱羧反应。
The onset of the great cause epilepsy quinolone drugs.
导致癫痫大发作的喹诺酮类药品。
Objective To make an analysis of quinolone adverse drug reaction (ADR).
目的分析喹诺酮类抗菌药物的不良反应(adr)。
AIM: To design and prepare quinolone compounds with antibacterial and antitumor activities.
目的：设计合成有抗菌抗肿瘤活性的喹诺酮药物。
OBJECTIVE to study the mutation in DNA gyrase a of Escherichia coli resistante to quinolone antibiotics.
目的研究导致大肠埃希菌dna回旋酶a亚单位的基因变异耐喹诺酮类药物的机制。
Do antibiotics sensitivity test on its recombinant strains, but no resistance of Quinolone can be found.
药敏试验结果表明，重组菌株失去对喹诺酮类药物的抗药性。
If there is an allergy to penicillin, physicians should consider azithromycin or a respiratory quinolone.
如果对青霉素过敏，医师们应该考虑阿奇霉素或呼吸喹诺酮。
Methods Retrospective analysis of 736 cases reported in the literature about quinolone adverse drug reaction was made.
方法采用回顾性分析的方法，对文献报道的736例喹诺酮类抗菌药物不良反应样本案例进行统计分析。
Objective To improve the synthesis of tetrafluorophthalic acid as an intermediate in preparing quinolone antibacterials.
目的合成喹诺酮类抗菌药中间体四氟邻苯二甲酸，并改进工艺，使之适用于工业化生产。
The spectroscopy analysis shows that all those quinolone drugs can react with BLf or HSA and form a drug-protein compound.
光谱分析结果表明，上述喹诺酮类药物都可以与牛乳铁蛋白或人血清白蛋白之间形成亲和力较强的复合物。
The contents of quinolone medicines such as ofloxacin etc in aqueous solution are analyzed by ion inhibition chromatography.
用离子抑制色谱进行水溶液中氧氟沙星等喹诺酮类药物含量的分析。
AIM to design and synthesize 1 (5 fluoro 2 pyridyl) quinolone derivatives, and to study their in vitro antibacterial activities.
目的设计合成1位为5氟2吡啶基的吡酮酸衍生物，并对其抗菌活性进行初步评价。
Quinolone drugs is a synthetic antibiotic, mainly used for infectious diseases in the field of treatment, antibacterial plays an important role.
喹诺酮类药品是一种人工合成的抗菌药，主要用于感染性疾病，在抗菌治疗领域发挥着重要作用。
Objective To study the unique cell-to-cell communication mechanism of Pseudomonas quinolone signal(PQS) in the pathogenesis of Pseudomonas aeruginosa.
目的研究细胞间信息传递机制之一假单胞菌喹诺酮信号（PQS）在铜绿假单胞菌发病机制中的作用。
Analysing the outer membrance protien of the 12 strains quinolone isolates with SDS-PAGE electrophoresis, and analysing the spreading trend with PFGE.
用脉冲场凝胶电泳对12株耐药菌进行了流行情况分析。
Norfloxacin is one of the outstanding representatives of the third generation of quinolone antibiotics, and there are a good deal of methods for synthesizing it.
氟哌酸是第三代喹诺酮类抗菌药物的优秀代表之一，它的合成路线有很多种，而以形成硼螯合物的方法倍受关注。
In this study, phosphoramide mustard was coupled to 2-phenyl-4-quinolone by a facile phosphorylation reaction to yield a novel quinoline-4-phosphoramidate derivative.
以2-苯基-4-喹啉酮为原料，通过磷酰化反应将磷酰氮芥引入到2-苯基-4-喹啉酮中，合成了一种新型的喹啉-4-氨基磷酸酯衍生物。
In 736 ADR cases reports of quinolone antibacterial agents, the nervous system was the most damage, followed by light toxicity, digestive system damage and cardiovascular system damage.
在736例喹诺酮类药物ADR中，以神经系统损害最多，其次是光毒性、消化系统损害、心血管系统损害等；
On the other hand, many commonly used drugs, including furafylline, fluvoxamine, quinolone antibacterial, agents verapamil, cimetidine and oral contraceptives, can inhibit CYP1A2 activity.
而许多临床常用的药物，如呋拉茶碱、氟伏沙明，喹诺酮类抗生素、维拉帕米、西米替丁和口服避孕药等，可抑制CYP1A2的活性。
Progresses on the synthesis and classification of the metal complexes based on quinolone antibacterial drugs, their structures, properties as well as their reaching trend in future are reviewed.
本文综述了喹诺酮类抗菌药物金属配合物的合成、分类、结构、性质等方面的研究现状，展望了此类研究的发展趋势。
Objective To investigate the impact of non target gene mutations and reduced permeability of the outer membrane on quinolone resistance and multiple antibiotic resistance (mar) in Escherichia coli.
目的：探讨非靶位基因突变及外膜通透性改变对大肠杆菌喹诺酮类耐药和多重耐药的影响。
Objective To investigate the impact of non target gene mutations and reduced permeability of the outer membrane on quinolone resistance and multiple antibiotic resistance (mar) in Escherichia coli.
目的：探讨非靶位基因突变及外膜通透性改变对大肠杆菌喹诺酮类耐药和多重耐药的影响。
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