| Weight | 318.304 g/mol |
|---|---|
| Formula | C16H15FN2O4 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Pazufloxacin (127045-41-4)
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- Spectroscopic studies on the interaction of pazufloxacin with calf thymus DNA (Journal of Photochemistry and Photobiology B-biology, 2008)
- Spectrophotometric studies on the interaction between pazufloxacin mesilate and human serum albumin or lysozyme (Journal of Luminescence, 2008)
- Preparation and characterization of glutaraldehyde cross-linked O-carboxymethylchitosan microspheres for controlled delivery of pazufloxacin mesilate (International Journal of Biological Macromolecules, 2007)
- Simultaneous measurement of pazufloxacin, ciprofloxacin, and levofloxacin in human serum by high-performance liquid chromatography with fluorescence detection. (Journal of Chromatography B, 2010)
- Reduced Clinical Efficacy of Pazufloxacin against Gonorrhea Due to High Prevalence of Quinolone-Resistant Isolates with the GyrA Mutation (Antimicrobial Agents and Chemotherapy, 1998)
- First liquid chromatography method for the simultaneous determination of levofloxacin, pazufloxacin, gatifloxacin, moxifloxacin and trovafloxacin in human plasma (Journal of Chromatography B, 2013)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1COC2=C3N1C=C(C(=O)C3=CC(=C2C4(CC4)N)F)C(=O)O
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InChIKeyXAGMUUZPGZWTRP-UHFFFAOYSA-N
- Pubchem - Pazufloxacin
- Wikipedia - pazufloxacin
Pazufloxacin (INN) is a fluoroquinolone antibiotic. It is sold in Japan under the brand names Pasil and Pazucross.
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Synthesis
KVVUTFTUKHKRKQ-UHFFFAOYSA-N
+
Reactant
(Friedel-Crafts alkylation)
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Pazufloxacin
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