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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.

In the Vinony graph

Vinony's link graph records 134 inbound references to enrofloxacin, and connects out to sulfamethazine, quinolone antibiotic and fidaxomicin.

It is catalogued under topics including Carboxylic acids, Cyclopropyl compounds and Drugboxes which contain changes to watched fields.

Vinony links it to 16 Wikipedia language editions.

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.

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