| Weight | 261.233 g/mol |
|---|---|
| Formula | C13H11NO5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
oxolinic acid (14698-29-4)
Gramurin · Sodium Oxolinate
Score:
#360 in Microbiology
,
#2884 in Biology
,
#3610 in Chemistry
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- DNA gyrase on the bacterial chromosome: DNA cleavage induced by oxolinic acid (Journal of Molecular Biology, 1979)
- Antibacterial activities of ciprofloxacin, norfloxacin, oxolinic acid, cinoxacin, and nalidixic acid. (Antimicrobial Agents and Chemotherapy, 1984)
- Residues of oxolinic acid and oxytetracycline in fish and sediments from fish farms (Aquaculture, 1991)
- Degradation of the antibiotic oxolinic acid by photocatalysis with TiO2 in suspension (Water Research, 2010)
- Digestibility of chloramphenicol, oxolinic acid and oxytetracycline in rainbow trout and influence of these antibiotics on lipid digestibility (Aquaculture, 1987)
- Synthesis, structure and biological activity of copper(II) complexes with oxolinic acid. (Journal of Inorganic Biochemistry, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H332: Harmful if inhaled
Warning Acute toxicity, inhalation - Category 4 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 - Gramurin
- Sodium Oxolinate
-
SMILESCCN1C=C(C(=O)C2=CC3=C(C=C21)OCO3)C(=O)O
-
InChIKeyKYGZCKSPAKDVKC-UHFFFAOYSA-N
- Pubchem - oxolinic acid
- Wikipedia - oxolinic acid
Oxolinic acid is a quinolone antibiotic developed in Japan in the 1970s. Dosages 1220mg/kg orally administered for five to ten days. The antibiotic works by inhibiting the enzyme DNA gyrase.
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oxolinic acid
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