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ChemicalBook--->CAS DataBase List--->878592-87-1

878592-87-1

878592-87-1 Structure

878592-87-1 Structure
IdentificationBack Directory
[Name]

3-Quinolinecarboxylic acid, 7-[(3E)-3-(2-aMino-1-fluoroethylidene)-1-piperidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-8-Methoxy-4-oxo-
[CAS]

878592-87-1
[Synonyms]

JNJ-Q2
Avarofloxacin
(E)-7-(3-(2-Amino-1-fluoroethylidene)piperidin-1-yl)-1-cyclopropyl-6-fluoro-8-methoxy-4-oxo-1
(E)-7-(3-(2-Amino-1-fluoroethylidene)piperidin-1-yl)-1-cyclopropyl-6-fluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
3-Quinolinecarboxylic acid, 7-[(3E)-3-(2-aMino-1-fluoroethylidene)-1-piperidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-8-Methoxy-4-oxo-
[Molecular Formula]

C21H23F2N3O4
[MDL Number]

MFCD18633282
[MOL File]

878592-87-1.mol
[Molecular Weight]

419.42
Chemical PropertiesBack Directory
[Boiling point ]

652.3±55.0 °C(Predicted)
[density ]

1.450±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:100.0(Max Conc. mg/mL);238.42(Max Conc. mM)
[form ]

Solid
[pka]

6.41±0.50(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

Avarofloxacin (JNJ-Q2) is a broad-spectrum fluoroquinolone antibacterial agent being developed for the treatment of acute bacterial skin and skin-structure infections and community-acquired pneumonia with oral activity. Avarofloxacin (JNJ-Q2) is an aminoethylidenylpiperidine fluoroquinolone that demonstrates antibacterial effect against numerous Gram-positive bacteria with a mean 0.12 mg/L MIC90 value. Avarofloxacin (JNJ-Q2) has potential for treatment of methicillin-resistant Staphylococcus aureus (MRSA) infections[1][2][3].
[IC 50]

Quinolone
[References]

[1] Jones TM, et al. Focus on JNJ-Q2, a novel fluoroquinolone, for the management of community-acquired bacterial pneumonia and acute bacterial skin and skin structure infections. DOI:10.2147/IDR.S105620
[2] Kocsis B, et al. Chemical structure and pharmacokinetics of novel quinolone agents represented by avarofloxacin, delafloxacin, finafloxacin, zabofloxacin and nemonoxacin. Ann Clin Microbiol Antimicrob. 2016 May 23;15(1):34. DOI:10.1186/s12941-016-0150-4
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