
CAS 97867-34-0: Norfloxacin lactate
Formula:C16H18FN3O3·C3H6O3
InChI:InChI=1S/C16H18FN3O3.C3H6O3/c1-2-19-9-11(16(22)23)15(21)10-7-12(17)14(8-13(10)19)20-5-3-18-4-6-20;1-2(4)3(5)6/h7-9,18H,2-6H2,1H3,(H,22,23);2,4H,1H3,(H,5,6)
InChI key:InChIKey=AYEXIHJJZPTXSS-UHFFFAOYSA-N
SMILES:C(C)N1C=2C(C(=O)C(C(O)=O)=C1)=CC(F)=C(C2)N3CCNCC3.C(C(O)=O)(C)O
Synonyms:- 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, mono(2-hydroxypropanoate)
- 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, compd. with 2-hydroxypropanoic acid (1:1)
- Propanoic acid, 2-hydroxy-, compd. with 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid (1:1)
- Norfloxacin lactate
Sort by
Found 1 products.
Norfloxacin lactate
CAS:Norfloxacin lactate is a synthetic antibacterial agent, derived from fluoroquinolone antibiotics, which acts by inhibiting bacterial DNA gyrase, an essential enzyme for DNA replication. This mode of action disrupts the supercoiling process required for bacterial DNA synthesis, leading to a bactericidal effect. Norfloxacin lactate is employed primarily for treating a range of infections caused by susceptible Gram-negative and some Gram-positive bacteria. Its applications are significant in the treatment of urinary tract infections, prostatitis, and certain types of gastrointestinal infections. The precise targeting of bacterial DNA replication processes imparts specificity, making it a valuable tool in clinical settings to combat bacterial resistance. Studies and clinical trials continue to explore its efficacy, dosage optimization, and resistance patterns to enhance its application in therapeutic strategies. Given its intricate mode of action, Norfloxacin lactate remains an important subject of pharmacokinetic and pharmacodynamic research.Formula:C19H24FN3O6Purity:Min. 95%Molecular weight:409.4 g/mol