| Weight | 262.221 g/mol |
|---|---|
| Formula | C12H10N2O5 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
cinoxacin (28657-80-9)
Cinobac · Azolinic Acid · Compound 64716
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- Separation of levofloxacin, ciprofloxacin, gatifloxacin, moxifloxacin, trovafloxacin and cinoxacin by high-performance liquid chromatography: application to levofloxacin determination in human plasma. (Journal of Chromatography B, 2002)
- Antibacterial activities of ciprofloxacin, norfloxacin, oxolinic acid, cinoxacin, and nalidixic acid. (Antimicrobial Agents and Chemotherapy, 1984)
- Interactions of metal ions with two quinolone antimicrobial agents (cinoxacin and ciprofloxacin): Spectroscopic and X-ray structural characterization. Antibacterial studies (Journal of Inorganic Biochemistry, 2002)
- Cinoxacin complexes with divalent metal ions. Spectroscopic characterization. Crystal structure of a new dinuclear Cd(II) complex having two chelate-bridging carboxylate groups. Antibacterial studies (Journal of Inorganic Biochemistry, 1998)
- Ni(II) and Zn(II) complexes with cinoxacin. Synthesis and characterization of M(Cx)2(DMSO)n(H2O)m (n=0, 2; m=2, 4). Crystal structures of [M(Cx)2(DMSO)2]4H2O (M=Ni(II), Zn(II)) (Inorganica Chimica Acta, 1993)
- Cross-resistance among cinoxacin, ciprofloxacin, DJ-6783, enoxacin, nalidixic acid, norfloxacin, and oxolinic acid after in vitro selection of resistant populations. (Antimicrobial Agents and Chemotherapy, 1984)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Cinobac
- Azolinic Acid
- Compound 64716
- Clinoxacin
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SMILESCCN1C2=CC3=C(C=C2C(=O)C(=N1)C(=O)O)OCO3
-
InChIKeyVDUWPHTZYNWKRN-UHFFFAOYSA-N
- Pubchem - cinoxacin
- Wikipedia - cinoxacin
Cinoxacin is a quinolone antibiotic that has been discontinued in the U.K. as well the United States, both as a branded drug or a generic. Cinoxacin was an older synthetic antimicrobial related to the quinolone class of antibiotics with activity similar to oxolinic acid and nalidixic acid.
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cinoxacin
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