Name: | temafloxacin |
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PubChem Compound ID: | 11640304 |
Molecular formula: | C21H18F3N3O3 |
Molecular weight: | 417.381 g/mol |
Name: | temafloxacin |
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Name (isomeric): | DB01405 |
Drug Type: | small molecule |
Synonyms: |
Temafloxacin hydrochloride; Temafloxacinum [latin]; Temafloxacina [spanish]; Temafloxacine [french]
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Brand: | Omniflox |
Category: | Anti-Bacterial Agents |
CAS number: | 108319-06-8 |
Indication: | For the treatment of lower respiratory tract infections, genital and urinary infections like prostatitis, and skin infections. |
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Pharmacology: |
Temafloxacin (marketed by Abbott Laboratories as Omniflox), is a fluoroquinolone antibiotic drug which was withdrawn from sale in the U.S. shortly after its approval in 1992 because of serious adverse reactions resulting in three deaths. Flouroquinolones such as lomefloxacin possess excellent activity against gram-negative aerobic bacteria such as ...
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Mechanism of Action: |
The bactericidal action of temafloxacin results from interference with the activity of the bacterial enzymes DNA gyrase and topoisomerase IV, which are needed for the transcription and replication of bacterial DNA. DNA gyrase appears to be the primary quinolone target for gram-negative bacteria. Topoisomerase IV appears to be the preferential targe...
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Absorption: | Studies in healthy volunteers indicate that the average bioavailability of temafloxacin exceeds 90%, with little intersubject variability. |
Biotransformation: | Hepatic. |
Half Life: | Approximately 8 hours in patients with normal renal function. |
Toxicity: | Severe adverse reactions, including allergic reactions and hemolytic anemia, developed in about fifty patients during the first four months of its use, leading to three patient deaths |
Affected organisms: | Enteric bacteria and other eubacteria |
Drug interaction: |
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