Weight | 359.401 g/mol |
---|---|
Formula | C19H22FN3O3 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 4 |
Enrofloxacin (93106-60-6)
Score:
#2278 in Biology
,
#2807 in Chemistry
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LabBot
- Phytotoxicity to and uptake of enrofloxacin in crop plants (Chemosphere, 2003)
- Pharmacokinetics and residues of enrofloxacin in chickens (American Journal of Veterinary Research, 1995)
- Pharmacokinetics of enrofloxacin and its metabolite ciprofloxacin after intravenous and oral administration of enrofloxacin in dogs (Journal of Veterinary Pharmacology and Therapeutics, 1993)
- Pharmacokinetics of enrofloxacin after single intravenous, intramuscular and subcutaneous injections in lactating cows. (Journal of Veterinary Pharmacology and Therapeutics, 1995)
- Spectrophotometric determination of ciprofloxacin, enrofloxacin and pefloxacin through charge transfer complex formation (Journal of Pharmaceutical and Biomedical Analysis, 2002)
- In vitro susceptibility of selected veterinary bacterial pathogens to ciprofloxacin, enrofloxacin and norfloxacin. (Canadian Journal of Veterinary Research-revue Canadienne De Recherche Veterinaire, 1990)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCN1CCN(CC1)C2=C(C=C3C(=C2)N(C=C(C3=O)C(=O)O)C4CC4)F
-
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- Pubchem - Enrofloxacin
- Wikipedia - enrofloxacin
Enrofloxacin (ENR) is a fluoroquinolone antibiotic sold by the Bayer Corporation under the trade name Baytril. Enrofloxacin is currently approved by the FDA for the treatment of individual pets and domestic animals in the United States. In September 2005, the FDA withdrew approval of Baytril for use in water to treat flocks of poultry, as this practice was noted to promote the evolution of fluoroquinolone-resistant strains of the bacterium Campylobacter, a human pathogen.
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