Delafloxacin

Delafloxacin
Systematic (IUPAC) name
1-(6-amino-3,5-difluoro-2-pyridyl)-8-chloro-6-fluoro-7-(3-hydroxyazetidin-1-yl)-4-oxo-quinoline-3-carboxylic acid
Clinical data
Legal status
  • Investigational
Identifiers
CAS Number 189279-58-1
ATC code None
PubChem CID 487101
ChemSpider 427049
UNII 6315412YVF YesY
KEGG D09330
ChEMBL CHEMBL2105637
Chemical data
Formula C18H12ClF3N4O4
Molar mass 440.76 g/mol

Delafloxacin (originally RX-3341) is a fluoroquinolone antibiotic being developed by Rib-X Pharmaceuticals, Inc.

It is more active (lower MIC90) than other quinolones against Gram-positive bacteria such as MRSA. In contrast to most approved fluoroquinolones, which are zwitterionic, delafloxacin has an anionic character, which results in a 10-fold increase in delafloxacin accumulation in both bacteria and cells at acidic pH. This property is believed to confer to delafloxacin an advantage for the eradication of Staphylococcus aureus in acidic environments, including intracellular infections.[1]

Clinical trials

Phase II clinical trials have been completed,[2][3][4] including a trial with tigecycline as a comparator[5] The company states delafloxacin met its primary and secondary efficacy endpoints based on the draft guidance from the FDA.

A Phase III trial for acute bacterial skin and skin structure infections (ABSSSI) is due to begin in the 2nd half of 2012.[6]

References

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