Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/32217
Title: Delafloxacin: design, development and potential place in therapy.
Authors: Candel, Francisco Javier
Peñuelas, Marina
Keywords: 
Mesh: 
Issue Date: 2017
Citation: Drug Des Devel Ther.2017;(11):881-891
Abstract: Delafloxacin (DLX) is a new fluoroquinolone pending approval, which has shown a good in vitro and in vivo activity against major pathogens associated with skin and soft tissue infections and community-acquired respiratory tract infections. DLX also shows good activity against a broad spectrum of microorganisms, including those resistant to other fluoroquinolones, as methicillin-resistant Staphylococcus aureus. Its pharmacokinetic properties and excellent activity in acidic environments make DLX an alternative in the treatment of these and other infections. In this manuscript, a detailed analysis of this new fluoroquinolone is performed, from its chemical structure to its in vivo activity in recently published clinical trials. Its possible place in the current antimicrobial outlook and in other infectious models is also discussed.
PMID: 28356714
URI: https://hdl.handle.net/20.500.12530/32217
Rights: openAccess
Appears in Collections:Fundaciones e Institutos de Investigación > IIS H. U. Clínico San Carlos > Artículos

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