Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C21H21FN4O3.ClH |
Molecular Weight | 432.876 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.[H][C@]12CN(C[C@@]1([H])NCCC2)C3=C(C#N)C4=C(C=C3F)C(=O)C(=CN4C5CC5)C(O)=O
InChI
InChIKey=WUPBAVNMWVWXBI-VFZPIINCSA-N
InChI=1S/C21H21FN4O3.ClH/c22-16-6-13-18(26(12-3-4-12)9-15(20(13)27)21(28)29)14(7-23)19(16)25-8-11-2-1-5-24-17(11)10-25;/h6,9,11-12,17,24H,1-5,8,10H2,(H,28,29);1H/t11-,17+;/m0./s1
Molecular Formula | C21H21FN4O3 |
Molecular Weight | 396.4148 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Pradofloxacin (trade name Veraflox) is a 3rd generation enhanced spectrum veterinary antibiotic of the fluoroquinolone class. It was developed by Bayer HealthCare AG, Animal Health GmbH, and received approval from the European Commission in April 2011 for prescription-only use in veterinary medicine for the treatment of bacterial infections in dogs and cats. The primary mode of action of fluoroquinolones involves interaction with enzymes essential for major DNA functions such as replication, transcription, and recombination. The primary targets for Pradofloxacin are the bacterial DNA gyrase and topoisomerase IV enzymes. Reversible association between Pradofloxacin and DNA gyrase or DNA topoisomerase IV in the target bacteria results in inhibition of these enzymes and rapid death of the bacterial cell. The rapidity and extent of bacterial killing are directly proportional to the drug concentration.
Originator
Sources: https://www.google.com/patents/WO1997031001A1
Curator's Comment: # Bayer Aktiengesellschaft
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Studies on a new device for drug delivery to the eye. | 2005 Feb |
|
In vivo tolerance and kinetics of a novel ocular drug delivery device. | 2006 Nov 28 |
|
Evaluation of the clinical efficacy of pradofloxacin tablets for the treatment of canine pyoderma. | 2010 Sep-Oct |
Patents
Sample Use Guides
Administer 3.0 mg/kg bodyweight of pradofloxacin once daily.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27449131
The MIC of pradofloxacinc was determined by broth microdilution according to Clinical and Laboratory Standards Institute (CLSI) standards,6 within the concentration range 0.008–16 μg/mL. The MICs of enrofloxacin and ciprofloxacin were determined using commercial stripsd on Mueller–Hinton 2 agar inoculated with a bacterial suspension (density of 0.5 McFarland) and incubated for 24 h at 35°C. The reference strain S. aureus ATCC 25923 was used as a quality control for MIC determination with the commercial strips, according to the manufacturer’s instructions.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:35:44 GMT 2023
by
admin
on
Sat Dec 16 19:35:44 GMT 2023
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Record UNII |
PX8LA4EH3R
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Record Status |
Validated (UNII)
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Record Version |
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9802883
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PX8LA4EH3R
Created by
admin on Sat Dec 16 19:35:44 GMT 2023 , Edited by admin on Sat Dec 16 19:35:44 GMT 2023
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ACTIVE MOIETY |
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