Temafloxacin
Temafloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair, producing bactericidal effects against a broad spectrum of gram-positive and gram-negative organisms. It was withdrawn from the market in 1992 due to a rare but serious syndrome of hemolytic anemia, hypoglycemia, and coagulopathy (temafloxacin syndrome). Its pharmacological mechanism is similar to other fluoroquinolones but its idiosyncratic toxicity profile led to permanent market withdrawal.
分子量
417.4000 g/mol
LogP
0.60
TPSA
72.90 Ų
リピンスキーの五則
適合
作用機序
Inhibits DNA topoisomerase, preventing the relaxation of supercoiled DNA during replication and transcription. This causes DNA strand breaks and triggers apoptosis in rapidly dividing cells.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits DNA topoisomerase, preventing the relaxation of supercoiled DNA during replication and transcription. This causes DNA strand breaks and triggers apoptosis in rapidly dividing cells.
2D構造
Cite this structure
Embed this structure
SMILES
CC1CN(c2cc3c(cc2F)c(=O)c(C(=O)O)cn3-c2ccc(F)cc2F)CCN1
InChI
InChI=1S/C21H18F3N3O3/c1-11-9-26(5-4-25-11)19-8-18-13(7-16(19)24)20(28)14(21(29)30)10-27(18)17-3-2-12(22)6-15(17)23/h2-3,6-8,10-11,25H,4-5,9H2,1H3,(H,29,30)
Molecular Formula
C21H18F3N3O3
HBD / HBA
2 / 9
回転可能結合数
3
重原子数
30
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
よくある質問
Temafloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair, producing bactericidal effects against a broad spectrum of gram-positive and gram-negative organisms. It was withdrawn from the market in 1992 due to a rare but serious syndrome of hemolytic anemia, hypoglycemia, and coagulopathy (temafloxacin syndrome). Its pharmacological mechanism is similar to other fluoroquinolones but its idiosyncratic toxicity profile led to permanent market withdrawal.
Inhibits DNA topoisomerase, preventing the relaxation of supercoiled DNA during replication and transcription. This causes DNA strand breaks and triggers apoptosis in rapidly dividing cells.
Yes, Temafloxacin is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL277100. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 60021. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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