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enrofloxacin

Structure via PubChem · Public domain (PubChem)

EntityQ414413· pop 17· linked from 134 articles

enrofloxacin

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Enrofloxacin, sold under the brand name Baytril, among others, is a fluoroquinolone antibiotic used for the treatment of animals. It is a bactericidal agent.

Chemical data

Formula
C19H22FN3O3
Molecular weight
359.4 g/mol
IUPAC name
1-cyclopropyl-7-(4-ethylpiperazin-1-yl)-6-fluoro-4-oxoquinoline-3-carboxylic acid
SMILES
CCN1CCN(CC1)C2=C(C=C3C(=C2)N(C=C(C3=O)C(=O)O)C4CC4)F
InChIKey
SPFYMRJSYKOXGV-UHFFFAOYSA-N
XLogP
-0.2
Polar surface area
64.1 Ų
H-bond donors
1
H-bond acceptors
7
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
359.165
Show 5 more facts
chemical formula
C₁₉H₂₂FN₃O₃
canonical SMILES
CCN1CCN(CC1)C2=C(C=C3C(=C2)N(C=C(C3=O)C(=O)O)C4CC4)F
Commons category
Enrofloxacin
subject has role
antineoplastic
medical condition treated
bacterial infectious disease
Sources (5)

via Wikidata · CC0

~3 min read

Encyclopedic overview

5 sections
Contents
  • Activity and susceptibility data
  • Adverse effects/warnings
  • Overdosage/acute toxicity
  • Degradation
  • References

Enrofloxacin, sold under the brand name Baytril, among others, is a fluoroquinolone antibiotic used for the treatment of animals. It is a bactericidal agent.

The bactericidal activity of enrofloxacin is concentration-dependent, with susceptible bacteria cell death occurring within 20–30 minutes of exposure. Enrofloxacin has demonstrated a significant post-antibiotic effect for both Gram-negative and Gram-positive bacteria and is active in both stationary and growth phases of bacterial replication. Enrofloxacin is partially deethylated by CYP450 into the active metabolite ciprofloxacin, which is also a fluoroquinolone antibiotic.

Excerpted from Wikipedia’s “enrofloxacin” article, available under the CC BY-SA 4.0 licence.