CAS 147059-72-1

Trovafloxacina

Descripción:

Trovafloxacina es un antibiótico fluoroquinolona sintético que exhibe una actividad antibacteriana de amplio espectro. Se utiliza principalmente para tratar diversas infecciones bacterianas, particularmente aquellas causadas por organismos Gram-positivos y Gram-negativos. El compuesto actúa inhibiendo la girasa del ADN bacteriano y la topoisomerasa IV, enzimas críticas para la replicación y transcripción del ADN, evitando así la división y el crecimiento celular bacteriano. Trovafloxacina se caracteriza por su potencia relativamente alta contra ciertos patógenos, incluidos aquellos resistentes a otros antibióticos. Se administra típicamente por vía oral o intravenosa y tiene un perfil farmacocinético favorable, lo que permite una dosificación una vez al día en muchos casos. Sin embargo, su uso se ha limitado debido a preocupaciones sobre la hepatotoxicidad y el potencial de efectos secundarios graves, lo que ha llevado a su retirada del mercado en algunas regiones. Además, al igual que otras fluoroquinolonas, puede estar asociado con riesgos de ruptura de tendones y efectos en el sistema nervioso central. En general, aunque Trovafloxacina demuestra propiedades antibacterianas efectivas, su perfil de seguridad requiere una consideración cuidadosa en el uso clínico.

Fórmula: C₂₀H₁₅F₃N₄O₃

InChI: InChI=1/C20H15F3N4O3/c21-8-1-2-15(13(22)3-8)27-7-12(20(29)30)17(28)9-4-14(23)19(25-18(9)27)26-5-10-11(6-26)16(10)24/h1-4,7,10-11,16H,5-6,24H2,(H,29,30)/t10-,11+,16+

Clave InChI: InChIKey=WVPSKSLAZQPAKQ-CDMJZVDBNA-N

SMILES: O=C1C=2C(N(C=C1C(O)=O)C3=C(F)C=C(F)C=C3)=NC(=C(F)C2)N4C[C@]5([C@@](C4)([C@@H]5N)[H])[H]

Sinónimos:

• (1α,5α,6α)-7-(6-Amino-3-azabi-cyclo[3.1.0]hex-3-y1)-1-(2,4-difluomphenyl)-6-fluom-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid
• 1,8-Naphthyridine-3-carboxylic acid, 7-(1.alpha.,5.alpha.,6.alpha.)-6-amino-3-azabicyclo3.1.0hex-3-yl-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-
• 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-
• 3-Azabicyclo[3.1.0]hexane, 1,8-naphthyridine-3-carboxylic acid deriv.
• 7-[(1R,5S)-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
• 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-1,8-naphthyridine-3-carboxylic acid
• Cp-99219
• Trovan：CP-99219-27
• Turvel
• Trovafloxacin
• 7-[(1R,5S)-6-azanyl-3-azabicyclo[3.1.0]hexan-3-yl]-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid
• 7-[(1R,5S)-6-amino-3-azabicyclo[3.1.0]hexan-3-yl]-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid

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-

CAS: 147059-72-1

Fórmula: C₂₀H₁₅F₃N₄O₃

Pureza: 98%

Forma y color: Solid

Peso molecular: 416.3533

Ref: IN-DA001EKY

Trovafloxacin

CAS: 147059-72-1

Fórmula: C₂₀H₁₅F₃N₄O₃

Peso molecular: 416.35

Ref: 7W-GP2666

Trovafloxacin

CAS: 147059-72-1

Trovafloxacin, a broad-spectrum quinolone antibiotic, exhibits potent activity against Gram-positive bacteria.

Fórmula: C₂₀H₁₅F₃N₄O₃

Pureza: 99.21% - 99.27%

Forma y color: Solid

Peso molecular: 416.35

Ref: TM-T13231

Trovafloxacin

Producto controlado

CAS: 147059-72-1

Applications Trovafloxacin is a fluroquinolone antibiotic, recently identified as an inhibitor of pannexin-1 (Panx1) channels. Trovafloxacin attenuates neuroinflammation and improves outcome after traumatic brain injury in mice.
References Garg, C., et al.: J. Neuroinflammation, 15, 42 (2018); Angus, J. A., et al.: Eur. J. Pharmacol., 791, 179 (2016)

Fórmula: C₂₀H₁₅F₃N₄O₃

Forma y color: Neat

Peso molecular: 402.37

Ref: TR-T892760

(1R,5R,6R)-7-(6-Amino-3-Azabicyclo[3.1.0]Hex-3- Yl)-1-(2,4-difluorophenyl)-6-Fluoro-1,4-dihydro-4-Oxo-1,8-naphthyridine-3-carbox

CAS: 147059-72-1

The mechanism of action of ciprofloxacin is to bind to the bacterial ribosome, thereby inhibiting protein synthesis. Ciprofloxacin is a broad-spectrum antibiotic that has been shown to be effective against both gram-positive and gram-negative bacteria, including methicillin resistant Staphylococcus aureus (MRSA). Ciprofloxacin is also active against Mycobacterium tuberculosis and Mycobacterium avium complex. It binds to the 30S ribosomal subunit, preventing attachment of aminoacyl tRNA. The addition of tetracycline can increase the activity of ciprofloxacin by inhibiting the efflux pump in the bacterial cell membrane. Ciprofloxacin has been found to have synergistic effects when used in combination with trovafloxacin or other antibiotics that act on different targets.

Fórmula: C₂₀H₁₅F₃N₄O₃

Pureza: Min. 95%

Forma y color: Powder

Peso molecular: 416.35 g/mol

Ref: 3D-FA103840