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QuickView for Temafloxacin (compound)


PubChem
Name: temafloxacin
PubChem Compound ID: 11640304
Molecular formula: C21H18F3N3O3
Molecular weight: 417.381 g/mol
DrugBank
Identification
Name: temafloxacin
Name (isomeric): DB01405
Drug Type: small molecule
Synonyms:
Temafloxacin hydrochloride; Temafloxacinum [latin]; Temafloxacina [spanish]; Temafloxacine [french]
Brand: Omniflox
Category: Anti-Bacterial Agents
CAS number: 108319-06-8
Pharmacology
Indication: For the treatment of lower respiratory tract infections, genital and urinary infections like prostatitis, and skin infections.
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Temafloxacin (marketed by Abbott Laboratories as Omniflox), is a fluoroquinolone antibiotic drug which was withdrawn from sale in the U.S. shortly after its approval in 1992 because of serious adverse reactions resulting in three deaths.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
Interactions
Drug interaction:
MagnesiumFormation of non-absorbable complexes
Iron DextranFormation of non-absorbable complexes
CalciumFormation of non-absorbable complexes

Targets


Enzymes