CAS 117707-40-1
:Desmethyl Levofloxacin
Description:
Desmethyl Levofloxacin, with the CAS number 117707-40-1, is a derivative of the fluoroquinolone antibiotic levofloxacin. It is characterized by its structural modification, specifically the absence of a methyl group at the nitrogen atom in the piperazine ring, which distinguishes it from its parent compound. This alteration can influence its pharmacological properties, including its antibacterial activity and spectrum of action. Desmethyl Levofloxacin exhibits broad-spectrum antimicrobial activity, primarily against Gram-negative and some Gram-positive bacteria, making it useful in treating various infections. The compound is typically administered in a form that allows for effective absorption and distribution in the body. Its mechanism of action involves the inhibition of bacterial DNA gyrase and topoisomerase IV, enzymes critical for bacterial DNA replication and transcription. Additionally, like other fluoroquinolones, it may have side effects and contraindications, necessitating careful consideration in clinical use. Overall, Desmethyl Levofloxacin represents an important compound in the study of antibiotic efficacy and resistance.
Formula:C17H18FN3O4
InChI:InChI=1/C17H18FN3O4/c1-9-8-25-16-13-10(15(22)11(17(23)24)7-21(9)13)6-12(18)14(16)20-4-2-19-3-5-20/h6-7,9,19H,2-5,8H2,1H3,(H,23,24)/t9-/m0/s1
SMILES:C[C@H]1COc2c3c(cc(c2N2CCNCC2)F)c(=O)c(cn13)C(=O)O
Synonyms:- (3S)-9-Fluoro-2,3-dihydro-3-methyl-7-oxo-10-(1-piperazinyl)-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic Acid
- Dn 5455
- (3S)-9-fluoro-3-methyl-7-oxo-10-piperazin-1-yl-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid
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Found 11 products.
Levofloxacin Related Compound A ((S)-9-fluoro-3-methyl-10-(piperazin-1-yl)-7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acid)
CAS:Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoiFormula:C17H18FN3O4Color and Shape:White PowderMolecular weight:347.12813Desmethyl Levofloxacin
CAS:Formula:C17H18FN3O4Purity:99%Color and Shape:SolidMolecular weight:347.3409Levofloxacin EP Impurity B (Levofloxacin USP Related Compound A, N-Desmethyl Levofloxacin)
CAS:Formula:C17H18FN3O4Color and Shape:Off-White To Pale Yellow SolidMolecular weight:347.35Desmethyl Levofloxacin
CAS:Desmethyl Levofloxacin, a levofloxacin metabolite, is a synthetic fluoroquinolone antibiotic that inhibits bacterial DNA gyrase.Formula:C17H18FN3O4Color and Shape:SolidMolecular weight:347.34Desmethyl Levofloxacin Hydrochloride
CAS:Controlled Product<p>Applications A metabolite of Levofloxacin.<br>References Sudo, K., et al.: Xenobiotica, 16, 72 (1986), Wong, F., et al.: Drug Metab. Dispos., 18, 1103 (1990), Aminimanizani, A., et al.: J. Clin. Pharmacokinet., 40, 169 (2001), Athamna, A., et al.: J. Antimicrob. Chemother., 53, 247 (2004), Tanaka, M., et al.: J. Pharmacol., 56, 463 (2004),<br></p>Formula:C17H18FN3O4•HClColor and Shape:NeatMolecular weight:347.3436469-Fluoro-3-methyl-7-oxo-10-(1-piperazinyl)-2,3-dihydro-7H-[1,4]oxazino[2,3,4-Ij]quinoline-6-carboxylic acid
CAS:<p>9-Fluoro-3-methyl-7-oxo-10-(1-piperazinyl)-2,3-dihydro-7H-[1,4]oxazino[2,3,4-Ij]quinoline (FQ) is a fluoroquinolone antibiotic. It inhibits the DNA gyrase and topoisomerase IV enzymes that maintain the integrity of bacterial DNA. FQ has been used to treat urinary tract infections in humans and other animals. This drug is also effective against methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. FQ binds to bacterial 16S ribosomal RNA and inhibits protein synthesis leading to cell death by inhibiting the production of proteins vital for cell division. The 9 position on the quinoline ring can be detected using UV detection at 260 nm.<br>FQ can be analyzed using mass spectrometry with fluor</p>Formula:C17H18FN3O4Purity:Min. 95 Area-%Color and Shape:White PowderMolecular weight:347.34 g/mol










