JNJ-Q2
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File:JNJ-Q2.svg | |
Systematic (IUPAC) name | |
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7-[(3E)-3-(2-Amino-1-fluoroethylidene)-1-piperidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid[1]
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Clinical data | |
Routes of administration |
Oral, IV |
Identifiers | |
ChemSpider | 9721013 |
Chemical data | |
Formula | C21H23F2N3O4 |
Molecular mass | 419.42 g/mol |
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JNJ-Q2 is a broad-spectrum fluoroquinolone antibacterial drug being developed for the treatment of acute bacterial skin and skin-structure infections and community-acquired pneumonia. Specifically, JNJ-Q2 is being actively studied for treatment of methicillin-resistant Staphylococcus aureus (MRSA) infections.[2][3]
Furiex Pharmaceuticals has licensed JNJ-Q2 from Janssen Pharmaceutica, a unit of Johnson & Johnson, which discovered JNJ-Q2. Furiex is responsible for its development and commercialization. Both oral and intravenous formulations are being developed.[4]
References
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- Cyclopropanes
- Piperidines
- Fluoroquinolone antibiotics
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