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Product Description
Mechanism of Action
Enoxacin gluconate is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, blocking supercoiling, replication and transcription of bacterial DNA. The gluconate form improves solubility.
Benefits and Advantages
Used in quinolone‑mechanism research, DNA‑gyrase assays, antimicrobial‑resistance modelling, and bacterial DNA‑topology studies.
Side Effects and Risks
Risks include tendon toxicity, CNS effects, QT prolongation, photosensitivity and dysglycemia. Handle with fluoroquinolone precautions.
Datasheet
| Molecular Formula | C15H17FN2O3·C6H12O7 |
|---|---|
| Molecular Weight | 516.5 g/mol |
| CAS Number | 85200-30-2 |
| Storage Condition | Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light. |
| Solubility | Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance. |
| Purity | Purity information is available upon request (COA). |
| Synonym | ENOXACIN GLUCONATE; Enoxacin glyconate; FK8O5WLR9H; Enoxacin gluconate [WHO-DD]; UNII-FK8O5WLR9H |
| IUPAC/Chemical Name | 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,8-naphthyridine-3-carboxylic acid;(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoic acid |
| InChl Key | UQCAODSJNCBXEG-IFWQJVLJSA-N |
| InChl Code | InChI=1S/C15H17FN4O3.C6H12O7/c1-2-19-8-10(15(22)23)12(21)9-7-11(16)14(18-13(9)19)20-5-3-17-4-6-20;7-1-2(8)3(9)4(10)5(11)6(12)13/h7-8,17H,2-6H2,1H3,(H,22,23);2-5,7-11H,1H2,(H,12,13)/t;2-,3-,4+,5-/m.1/s1 |
| References |
3D Conformer.
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