CAS 112984-60-8
:6-Fluoro-1-Methyl-4-Oxo-7-(1-Piperazinyl)-4H-(1,3)-Thiazeto(3,2-Alpha)Quinoline-3-Carboxylic Acid
Description:
6-Fluoro-1-Methyl-4-Oxo-7-(1-Piperazinyl)-4H-(1,3)-Thiazeto(3,2-Alpha)Quinoline-3-Carboxylic Acid, with CAS number 112984-60-8, is a synthetic compound characterized by its complex heterocyclic structure, which includes a quinoline core fused with a thiazole ring. The presence of a fluorine atom at the 6-position and a piperazine moiety at the 7-position contributes to its unique pharmacological properties. This compound typically exhibits a range of biological activities, making it of interest in medicinal chemistry, particularly in the development of antimicrobial or antitumor agents. Its carboxylic acid functional group may enhance solubility and bioavailability, while the oxo group can participate in various chemical reactions. The compound's structural features suggest potential interactions with biological targets, which can be explored further in drug discovery research. Overall, this substance represents a class of compounds that may offer therapeutic benefits, although specific applications and efficacy would require detailed experimental investigation.
Formula:C16H16FN3O3S
InChI:InChI=1/C16H16FN3O3S/c1-8-20-11-7-12(19-4-2-18-3-5-19)10(17)6-9(11)14(21)13(16(22)23)15(20)24-8/h6-8,18H,2-5H2,1H3,(H,22,23)
InChI key:InChIKey=SUXQDLLXIBLQHW-UHFFFAOYSA-N
SMILES:CC1N2C=3C(C(=O)C(C(O)=O)=C2S1)=CC(F)=C(C3)N4CCNCC4
Synonyms:- 1H,4H-[1,3]Thiazeto[3,2-a]quinoline-3-carboxylic acid, 6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-
- 1H,4H-[1,3]Thiazeto[3,2-a]quinoline-3-carboxylicacid,6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)
- 6-Fluoro-1-Methyl-4-OXO-7-(1-PIPRAZINYL)-4H-(1,3)-THIAZETO(3,2-A)quinoline-3-CAR
- 6-Fluoro-1-Methyl-4-Oxo-7-(1-Piperazinyl)-4H-(1,3)Thiazeto(3,2-A)Quinoline-3-Carboxylicacid
- 6-Fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3) -thiazeto (3,2-a)quinoline-3-carboxylic acid
- 6-Fluoro-1-methyl-4-oxo-7-piperazin-1-yl-4H-2-thia-8b-aza-cyclobuta[a] naphthalene-3-carboxylic acid
- 6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-1H,4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid
- 6-fluoro-1-methyl-4-oxo-7-(piperazin-1-yl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid
- Af 3013
- Nad 394
- Nm 394
- Pl-11
- Ulifloxacin
- Prulifloxacin Intermediate PL-11
- 6-Fluoro-1-methyl-7-(1-piperazinyl)-4-oxo-4H-(1,3)thiazeto(3,2-a)quinoline-3-carboxylic acid
- 6-FLUORO-7-PIPERAZINE-1-METHYL-4-OXY-[1,3]THIOAZACYCLIC[3,2-A]-QUINOLINE-3-CARBOXYLIC ACID
- PRULIFLOXACIN INTERMEDIATE 3
- 6-Fluoro-1-Methyl-4-Oxo-7-(1-Piperazinyl)-4H-(1,3)-Thiazeto(3,2-Alpha)Quinoline-3-Carboxylic Acid
- 6-Fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3)-thiazeto
- 6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3)-thiazeto(3,2-a)quinoline-3-carboxylic acid cas:(intermediate of prulifloxacin)
- 6-FLUORO-1-METHYL-4-OXO-7-(1-PIPRAZINYL)-1H,4H-(1,3)THIAZETO(3,2-A)QUINOLINE-3-CARBOXYLIC ACID
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Found 7 products.
6-Fluoro-1-methyl-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid
CAS:Formula:C16H16FN3O3SPurity:95%Color and Shape:SolidMolecular weight:349.37996-Fluoro-1-methyl-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid
CAS:<p>6-Fluoro-1-methyl-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid</p>Purity:95%Molecular weight:349.39g/molUlifloxacin
CAS:<p>Applications A metabolite of Prulifloxacin (P838885). Ulifloxacin is a new quinolone antibiotic and it is effective against pneumonia.<br>References Kim, D., et al.: J. Pharm. Sci., 77, 200 (1988), Suzuki, T., et al.: Drug Metab. Dispos., 30, 1393 (2002), Sun, J., et al.: Eur. J. Pharm. Biopharm., 64, 238 (2006),<br></p>Formula:C16H16FN3O3SColor and Shape:NeatMolecular weight:349.38Ulifloxacin
CAS:<p>Extensive research has been conducted on the antimicrobial activity of 6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3)thiazeto(3,2a)quinoline-3-carboxylic acid (FPMT). FPMT is a levorotatory compound that is rapidly metabolized by esterases to 6FMT, which is also active against bacteria. FPMT inhibits bacterial growth, but does not inhibit mammalian cell growth. The main mechanism of action for FPMT is probably through its ability to inhibit the synthesis of bacterial DNA and RNA. This drug has been shown to be effective against sinusitis caused by bacterial rhinosinusitis and urinary tract infections caused by Escherichia coli and Pseudomonas aeruginosa. FPMT can be used as an alternative to prulifloxacin for the treatment of these types of infections</p>Formula:C16H16FN3O3SPurity:Min. 98 Area-%Molecular weight:349.38 g/molUlifloxacin
CAS:<p>Ulifloxacin is a useful organic compound for research related to life sciences. The catalog number is T65577 and the CAS number is 112984-60-8.</p>Formula:C16H16FN3O3SColor and Shape:SolidMolecular weight:349.38







