CAS 147059-75-4
:Mesilato di trovafloxacina
- 1,8-Naphthyridine-3-carboxylic acid, 7-(6-amino-3-azabicyclo[3.1.0]hex-3-yl)-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-, (1α,5α,6α)-, monomethanesulfonate
- 1,8-Naphthyridine-3-carboxylic acid, 7-[(1α,5α,6α)-6-amino-3-azabicyclo[3.1.0]hex-3-yl]-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-, methanesulfonate (1:1)
- 3-Azabicyclo[3.1.0]hexane, 1,8-naphthyridine-3-carboxylic acid deriv.
- 7-[(1R,5S,6s)-6-amino-3-azabicyclo[3.1.0]hex-3-yl]-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid methanesulfonate (1:1)
- Cp 99219
- Cp 99219-27
- Trovafloxacin Mesylate
- Trovafloxacin methanesulfonate
- Trovafloxacin monomethanesulfonate
- Trovan
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Trovafloxacin mesylate
CAS:Trovafloxacin mesylateFormula:C21H19F3N4O6SPurezza:≥98%Peso molecolare:512.46rel-7-((1R,5S,6s)-6-Amino-3-azabicyclo[3.1.0]hexan-3-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid compound with methanesulfonic acid (1:1)
CAS:Formula:C21H19F3N4O6SPurezza:99%Colore e forma:SolidPeso molecolare:512.4590Trovafloxacin Mesylate
CAS:Prodotto controllatoApplications Fluorinated quinolone antibacterial. Trovafloxacin mesylate blocks the activity of DNA gyrase and topoisomerase IV, enzymes essential in the repliction, transcription, and repair of bacterial DNA.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Neu, H.C., et al.: Clin. Antimicrob. Agents Chemother., 38, 2615 (1994), Liguori, M.J., et al.: Hepatology, 41, 177 (2005),Formula:C20H15F3N4O3·CH4O3SColore e forma:NeatPeso molecolare:512.46Trovafloxacin mesylate
CAS:rel-7-((1R,5S,6s)-6-Amino-3-azabicyclo[3.1.0]hexan-3-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid compound with methanesulfonic acid (1:1)Formula:C21H19F3N4O6SPurezza:99%Peso molecolare:512.46Trovafloxacin mesylate
CAS:Trovafloxacin mesylate is a synthetic antibiotic belonging to the fluoroquinolone class, which is derived from chemical synthesis processes rather than natural sources. The mode of action of trovafloxacin mesylate involves the inhibition of bacterial enzymes DNA gyrase and topoisomerase IV. These enzymes are essential for DNA replication, repair, and transcription within the bacterial cell. By inhibiting these enzymes, trovafloxacin mesylate disrupts bacterial DNA processes, leading to cell death and exerting its antibacterial effects.
Formula:C21H19F3N4O6SPurezza:Min. 95%Peso molecolare:512.46 g/molTrovafloxacin mesylate
CAS:Trovafloxacin: broad-spectrum fluoroquinolone, blocks DNA gyrase/topoisomerase IV and PANX1 channel (IC50=4μM).Formula:C21H19F3N4O6SPurezza:99.18%Colore e forma:SolidPeso molecolare:512.46






