ENOXACIN GLUCONATE
Enoxacin gluconate is a fluoroquinolone antibiotic that inhibits DNA gyrase. Side effects include tendonitis, GI upset, and CNS stimulation. Only GMP materials will be supplied, logistics all according to GDP.
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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 quinolonemechanism research, DNAgyrase assays, antimicrobialresistance modelling, and bacterial DNAtopology studies.
Side Effects and Risks
Risks include tendon toxicity, CNS effects, QT prolongation, photosensitivity and dysglycemia. Handle with fluoroquinolone precautions.
Only GMP materials will be supplied, logistics all according to GDP.
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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