| Weight | 385.37 g/mol |
|---|---|
| Formula | C20H17F2N3O3 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
Sarafloxacin (98105-99-8)
Score:
#447 in Biochemistry
,
#1465 in Biology
,
#1717 in Chemistry
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- Comparative single-dose pharmacokinetics of four quinolones, oxolinic acid, flumequine, sarafloxacin, and enrofloxacin, in Atlantic salmon (Salmo salar) held in seawater at 10 degrees C. (Antimicrobial Agents and Chemotherapy, 1995)
- Aerobic biodegradation of (14C)sarafloxacin hydrochloride in soil (Environmental Toxicology and Chemistry, 1997)
- In Vitro Resistance by Fish Pathogens to Aquacultural Antibacterials, Including the Quinolones Difloxacin (A-56619) and Sarafloxacin (A-56620) (Journal of Aquatic Animal Health, 1989)
- Production and characterization of monoclonal antibodies against sarafloxacin and cross-reactivity studies of related fluoroquinolones (Journal of Agricultural and Food Chemistry, 1997)
- Photolysis of difloxacin and sarafloxacin in aqueous systems (Chemosphere, 2009)
- In vitro residual anti-bacterial activity of difloxacin, sarafloxacin and their photoproducts after photolysis in water (Environmental Pollution, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CN(CCN1)C2=C(C=C3C(=C2)N(C=C(C3=O)C(=O)O)C4=CC=C(C=C4)F)F
-
InChIKeyXBHBWNFJWIASRO-UHFFFAOYSA-N
- Pubchem - Sarafloxacin
- Wikipedia - sarafloxacin
Sarafloxacin (INN) is a quinolone antibiotic drug, which was removed from clinical use by its manufacturer Abbott Laboratories from April 30, 2001.
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