[1]Arjona A.Nemonoxacin:quinolone antibiotic[J].Drugs Future, 2009, 34(3):196-203.
[2]Lu T,Zhao X,Li X.Enhancement of fluoroquinolone activity by C8 halogen and methoxy moieties: action against a gyrase resistance mutant of Mycobacterium smegmatis and a gyrasetopoisomerase IV double mutant of Staphylococcus aureus[J].Antimicrob Agents Chemother,2001,45:2703-2709.
[3]Takahata M,Yonezawa M, Kurose S, et al. Mutations in the gyrA and grlA genes of quinoloneresistant clinical isolates of methicillinresistant Staphylococcus aureus[J]. J Antimicrob Chemother,1996,38 (3): 543-546.
[4]李宵宁,柴芸,刘明亮. 喹诺酮类抗菌药的作用机制及耐药机制研究进展[J].国外医药:抗生素分册,2015,36(3):97-102.
[5]范柏. 喹诺酮类抗菌药的作用机制及细菌耐药性的研究进展[J].国外医药:抗生素分册,2004,25(1):27-29.
[6]Qin X,Huang H. Review of nemonoxacin with special focus on clinical development[J]. Drug Devel Ther,2014,8:765-747.
[7]蒋萍,陈恒屹,张坚磊,等. 耐喹诺酮类大肠埃希菌耐药机制的研究[J].中华医院感染学杂志,2017,17(6):635-638.
[8]Ferrero L,Cameron B,Manse B,et al.Cloning and primary structure of Staphylococcus aureus DNA topoisomerase Ⅳ:A primary target of fluoroquinolones[J].Mol Microbiol,1994,13(4):641-653.
[9]Roychoudhury S,Makin K,Twinem T,et al.In vitro resistance development to nemonoxacin in streptococcus pneumonia:A unique profile for a novel onfluorinated quinolone[J].Microb Drug Resist,2016,22(7):578-584.
[10]刘明亮,郭慧元.非氟喹诺酮的发现、构效关系及其特性[J].国外医药:抗生素分册,2006,27(1):16-21. |