Enrofloxacin

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Structural formula
Structure of enrofloxacin
General
Non-proprietary name Enrofloxacin
other names

1-Cyclopropyl-7- (4-ethylpiperazin-1-yl) -6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Molecular formula C 19 H 22 FN 3 O 3
External identifiers / databases
CAS number 93106-60-6
EC number 618-911-2
ECHA InfoCard 100.131.355
PubChem 71188
ChemSpider 64326
Wikidata Q414413
Drug information
ATC code

Q J01MA90

Drug class

Antibiotics

Mechanism of action

Gyrase inhibitors

properties
Molar mass 359.39 g · mol -1
safety instructions
Please note the exemption from the labeling requirement for drugs, medical devices, cosmetics, food and animal feed
GHS labeling of hazardous substances
no GHS pictograms
H and P phrases H: no H-phrases
P: no P-phrases
Toxicological data

4336 mg kg −1 ( LD 50mouseoral )

As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Enrofloxacin is an antibiotic from the group of active substances called fluoroquinolones .

properties

Enrofloxacin is a gyrase inhibitor and has a bactericidal effect . There is high bioavailability after both oral and parenteral administration . Elimination occurs primarily via the kidneys . The half-lives are between 2 and 7 hours depending on the species, the main metabolite is ciprofloxacin .

application areas

Enrofloxacin is used as an anti- infectious agent for the treatment of infectious diseases in dogs , chickens , calves , cats , cattle , small pets , turkeys , fattening rabbits and pigs . It has a good effect against a large number of gram-negative and gram-positive bacteria , including Escherichia coli , Erysipelothrix rhusiopathiae ( swine rotlauf ), Haemophilus spp., Salmonella spp., Mycoplasmas ( M. bovis & M. hyopneumoniae ), Pasteurella spp. and staphylococci . Depending on the species, the focus is on the treatment of specific diseases :

Interactions

The simultaneous use of chloramphenicol , tetracyclines or macrolide antibiotics can lead to antagonistic effects. If there is resistance to quinolones, there is no effectiveness because there is cross-resistance to all fluoroquinolones. If streptococcal infection is proven, it should not be used due to its low effectiveness.

Application forms

Enrofloxacin can be administered intravenously , subcutaneously or orally as a solution or tablet.

Side effects

Growing dogs and turkeys in particular have a particular sensitivity to enrofloxacin. This leads to severe damage to the cartilage growth, so that use in this age group is generally not permitted ( contraindicated ). Gastrointestinal disturbances and (with high doses ) local reactions at the injection site may also occur as side effects.

Trade names

Avoczol, Baytril, Colmyc, Doraflox, Enrobactin, Enro-K, Enro-Sleecol, Enroflox, Enrostar, Enrotab, Enrotril, Enrotron, Enrox, Enroxil, Fenoflox, Floxibac, Lanflox, Orniflox, Powerflox, Roxacin, Spectoflox, Roxacin, Xeden

Individual evidence

  1. a b c data sheet enrofloxacin from Sigma-Aldrich , accessed on May 13, 2017 ( PDF ).

Web links

  • Entry on Enrofloxacin at Vetpharm, accessed August 4, 2012.