Garenoxacin Mesylate
This mesylate salt form of garenoxacin is an oral fluoroquinolone antibiotic used primarily for community-acquired pneumonia and other respiratory infections. It has a broad spectrum of antibacterial activity including coverage of resistant respiratory pathogens.
Masse moléculaire
540,5000 g/mol
TPSA
143,00 Ų
Mécanisme d'action
Inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair. This leads to breakage of bacterial chromosomal DNA and rapid cell death.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair. This leads to breakage of bacterial chromosomal DNA and rapid cell death.
Structure 2D
Cite this structure
Embed this structure
SMILES
CS(=O)(=O)O.C[C@H]1NCc2cc(-c3ccc4c(=O)c(C(=O)O)cn(C5CC5)c4c3OC(F)F)ccc21.O
InChI
InChI=1S/C23H20F2N2O4.CH4O3S.H2O/c1-11-15-5-2-12(8-13(15)9-26-11)16-6-7-17-19(21(16)31-23(24)25)27(14-3-4-14)10-18(20(17)28)22(29)30;1-5(2,3)4;/h2,5-8,10-11,14,23,26H,3-4,9H2,1H3,(H,29,30);1H3,(H,2,3,4);1H2/t11-;;/m1../s1
Molecular Formula
C24H26F2N2O8S
HBD / HBA
4 / 12
Liaisons Rotatives
5
Atomes Lourds
37
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.
Foire aux questions
This mesylate salt form of garenoxacin is an oral fluoroquinolone antibiotic used primarily for community-acquired pneumonia and other respiratory infections. It has a broad spectrum of antibacterial activity including coverage of resistant respiratory pathogens.
Inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair. This leads to breakage of bacterial chromosomal DNA and rapid cell death.
Yes, Garenoxacin Mesylate 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). CHEMBL3183451. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 157690. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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