
CAS 97867-33-9: Ciprofloxacin lactate
Formula:C17H18FN3O3·C3H6O3
InChI:InChI=1S/C17H18FN3O3.C3H6O3/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24;1-2(4)3(5)6/h7-10,19H,1-6H2,(H,23,24);2,4H,1H3,(H,5,6)
InChI key:InChIKey=NRBJWZSFNGZBFQ-UHFFFAOYSA-N
SMILES:O=C1C=2C(N(C=C1C(O)=O)C3CC3)=CC(=C(F)C2)N4CCNCC4.C(C(O)=O)(C)O
Synonyms:- 1-Cyclopropyl-6-Fluoro-4-Oxo-7-(Piperazin-1-Yl)-1,4-Dihydroquinoline-3-Carboxylic Acid - 2-Hydroxypropanoic Acid (1:1)
- 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid lactate
- 3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, 2-hydroxypropanoate (1:1)
- 3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-, mono(2-hydroxypropanoate)
- Propanoic acid, 2-hydroxy-, compd. with 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid (1:1)
- Ciprofloxacin lactate
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Found 9 products.
Ciprofloxacin Lactate
CAS:Controlled ProductApplications Ciprofloxacin Lactate is an antibiotic that has been used to medicate polymer wound dressing. Ciprofloxacin Lactate has been shown to produce high and sustained serum bactericidal titers against highly susceptible bacteria. References Yu, H., et. al.: J. Appl. Polymer Sci., 101, 2453 (2006); Dudley, M.N., et. al.: DICP, Annals, Pharmacotherapy, 23, 456 (1989)Formula:C17H18FN3O3·C3H6O3Color and Shape:NeatMolecular weight:421.421-Cyclopropyl-6-Fluoro-4-Oxo-7-(Piperazin-1-Yl)-1,4-Dihydroquinoline-3-Carboxylic Acid 2-Hydroxypropanoic Acid Salt
CAS:1-Cyclopropyl-6-Fluoro-4-Oxo-7-(Piperazin-1-Yl)-1,4-Dihydroquinoline-3-Carboxylic Acid 2-Hydroxypropanoic Acid SaltPurity:97%Molecular weight:421.42g/molCiprofloxacin lactate
CAS:Ciprofloxacin lactate is a useful organic compound for research related to life sciences. The catalog number is T66299 and the CAS number is 97867-33-9.Formula:C20H24FN3O6Color and Shape:SolidMolecular weight:421.425Ciprofloxacin lactate
CAS:Ciprofloxacin is a broad-spectrum antibiotic that inhibits bacterial DNA synthesis. Ciprofloxacin is highly stable and has a long half-life. It is used to treat infections such as urinary tract infections, prostatitis, and pneumonia. Ciprofloxacin binds to the bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. The reaction mechanism of ciprofloxacin lactate is similar to that of other fluoroquinolones in inhibiting bacterial DNA gyrase and topoisomerase IV, which are enzymes that maintain the integrity of bacterial DNA. This drug also has antimicrobial activity against both Gram-positive and Gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA).Formula:C17H18FN3O3•C3H6O3Purity:Min. 95%Color and Shape:PowderMolecular weight:421.42 g/mol1-Cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid compound with 2-hydroxypropanoic acid (1:1)
CAS:Formula:C20H24FN3O6Purity:99%Color and Shape:SolidMolecular weight:421.4195Ciprofloxacin Lactate
CAS:Formula:C17H18FN3O3·C3H6O3Color and Shape:Off-White SolidMolecular weight:331.35 90.08