Drug Name: | Ofloxacin (82419-36-1) |
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PubChem ID: | 4583 |
SMILES: | CC1COC2=C3N1C=C(C(=O)C3=CC(=C2N4CCN(CC4)C)F)C(=O)O |
InchiKey: | GSDSWSVVBLHKDQ-UHFFFAOYSA-N |
Therapeutic Category: | Anti-Bacterial Agents, Anti-Infective Agents, Antineoplastic Agents, Cytochrome P-450 CYP1A2 Inhibitors, Cytochrome P-450 Enzyme Inhibitors, Enzyme Inhibitors, Nucleic Acid Synthesis Inhibitors, Renal Agents, Topoisomerase II Inhibitors, Topoisomerase Inhibitors |
Molecular Weight (dalton) | : | 361.373 |
LogP | : | 1.544 |
Ring Count | : | 2 |
Hydrogen Bond Acceptor Count | : | 6 |
Hydrogen Bond Donor Count | : | 1 |
Total Polar Surface Area | : | 75.01 |
This panel provides information on interacting drugs and their ADRs along with references
Interacting drug | Toxicity | Interaction Type | Mechanism | Reference |
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Fenbufen (36330-85-5) | Convulsions | Antagonistic | Not fully understood Experiments in mice have shown that quinolones competitively inhibit the binding of gamma-amino butyric acid (GABA) to its receptors the NSAID simply lowers the amount of quinolone needed to precipitate convulsions in already susceptible individuals | Effects of ketoprofen (NSAID) on the pharmacokinetics of pefloxacin and ofloxacin in healthy volunteers |
Warfarin (81-81-2) | Bleeding | Antagonistic | Uncertain. It is not clear what factors might have been responsible in those cases where the effects of the anticoagulants were increased | Ofloxacin and warfarin |
This panel provides drug-protein interaction and their ADRs along with references
Toxicity | Interacting Protein | Mechanism | Reference |
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This panel provides drug-food interactions and their ADRs along with references
Food | Toxicity | Reference |
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This panel provides information on metabolites and their ADRs along with references
Metabolite | Toxicity | Place of Metabolism | Mechanism | Reference |
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This panel provides information on drug category