For research use only. Not for therapeutic Use.
Ciprofloxacin Hydrochloride（Cat No.:R023314）is a broad-spectrum antibiotic belonging to the fluoroquinolone class, widely used to treat various bacterial infections. It works by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication, transcription, and repair, leading to bacterial cell death. Ciprofloxacin Hydrochloride is effective against both Gram-negative and Gram-positive bacteria and is commonly used for respiratory, urinary tract, and skin infections. Its high bioavailability and potent antibacterial action make it a valuable agent in clinical settings for combating bacterial resistance and treating severe infections.
| Catalog Number | R023314 |
| CAS Number | 86393-32-0 |
| Synonyms | 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic Acid Hydrochloride; Bay Q3939 Hydrochloride; |
| Molecular Formula | C17H21ClFN3O4 |
| Purity | ≥95% |
| Storage | Store at -20°C |
| IUPAC Name | 1-cyclopropyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid;hydrate;hydrochloride |
| InChI | InChI=1S/C17H18FN3O3.ClH.H2O/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24;;/h7-10,19H,1-6H2,(H,23,24);1H;1H2 |
| InChIKey | ARPUHYJMCVWYCZ-UHFFFAOYSA-N |
| SMILES | C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=O)O.O.Cl |
| Reference | <p>Wolfson, John S., and David C. Hooper. /The Fluoroquinolones: Structures, Mechanisms of Action and Resistance, and Spectra of Activity in Vitro./ <em>American Society for Microbiology</em> 4th ser. 28 (1985): 581-86.</p><p>Fellner M. Influence of the antibiotic ciprofloxacin on culture of Allium longicuspis callus-derived protoplasts. Annals of Botany 76: 219-223, 1995.</p></span></p> |
