
6-Fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3)thiazeto(3,2-a)quinoline-3-carboxylic acid
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Category:Active Pharmaceutical Ingredients Own Brand:MT /MOQ:100KG /From China/ B2B only.
Introduction
Catalog ID80017579
CAS NO.112984-60-8
Purity 95%
MDL NumberMFCD00882994
EINEC Molecular Formula C16H16FN3O3S
Molecular Weight 349.3799
| Aspect | Details |
|---|---|
| Chemical Structure | 6-Fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3)thiazeto(3,2-a)quinoline-3-carboxylic acid |
| Related Compounds | – Ciprofloxacin: 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid<br>- 1-Benzyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-quinoline-3-carboxylic acid |
| Structural Features | – Contains a quinoline core with a piperazine moiety.<br>- Substituted with a methyl group and a fluorine atom.<br>- Contains a thiazetidine ring (4H-(1,3)thiazeto) which is unique compared to other quinolones. |
| Potential Applications | – Likely to have antibacterial or antimicrobial properties due to the quinoline core and piperazine group.<br>- May be a derivative or analog of known quinolone antibiotics like ciprofloxacin. |
| Synthesis | – Likely synthesized through multi-step organic synthesis involving quinoline, piperazine, and thiazetidine ring formation.<br>- Specific synthesis routes would require detailed chemical procedures. |
| Pharmacological Properties | – Antibacterial Activity: Potentially effective against Gram-positive and Gram-negative bacteria.<br>- Mechanism of Action: Likely inhibits bacterial DNA gyrase or topoisomerase IV, similar to other quinolones. |
| Research Status | – Limited information available; likely a research compound or a derivative of known quinolone antibiotics.<br>- Further studies required to determine its efficacy, safety, and potential clinical applications. |
| Storage Conditions | – Likely stored in a cool, dry place, protected from light and moisture, similar to other quinolone compounds. |
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