Weight | 361.373 g/mol |
---|---|
Formula | C18H20FN3O4 |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
LEVOFLOXACIN (100986-85-4)
Score:
#28 in Microbiology
,
#534 in Biology
,
#567 in Chemistry
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- Pharmacodynamics of levofloxacin: a new paradigm for early clinical trials. (JAMA, 1998)
- Resistance to levofloxacin and failure of treatment of pneumococcal pneumonia (The New England Journal of Medicine, 2002)
- Levofloxacin to Prevent Bacterial Infection in Patients with Cancer and Neutropenia (The New England Journal of Medicine, 2005)
- A multicenter, randomized study comparing the efficacy and safety of intravenous and/or oral levofloxacin versus ceftriaxone and/or cefuroxime axetil in treatment of adults with community-acquired pneumonia. (Antimicrobial Agents and Chemotherapy, 1997)
- The clinical pharmacokinetics of levofloxacin. (Clinical Pharmacokinectics, 1997)
- Comparison of the antibacterial activities of the quinolones Bay 12-8039, gatifloxacin (AM 1155), trovafloxacin, clinafloxacin, levofloxacin and ciprofloxacin. (Journal of Antimicrobial Chemotherapy, 1997)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1COC2=C3N1C=C(C(=O)C3=CC(=C2N4CCN(CC4)C)F)C(=O)O
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InChIKeyGSDSWSVVBLHKDQ-UHFFFAOYSA-N
- Pubchem - LEVOFLOXACIN
- Wikipedia - levofloxacin anhydrous
Levofloxacin, sold under the trade names Levaquin among others, is an antibiotic. It is used to treat a number of bacterial infections including acute bacterial sinusitis, pneumonia, urinary tract infections, chronic prostatitis, and some types of gastroenteritis. Along with other antibiotics it may be used to treat tuberculosis, meningitis, or pelvic inflammatory disease.
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