211690-33-4
Chemical Structure
Lomefloxacin (aspartate)
Synonym(s): SC47111A (aspartate);NY-198 (aspartate)
- CAS No.: 211690-33-4
- Formula:C21H26F2N4O7
- Molecular Weight:484.45
IUPAC Name: L-aspartic acid compound with 1-ethyl-6,8-difluoro-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (1:1)
InChIKey: YCOJCBAVYZZKRS-WNQIDUERSA-N
SMILES: N[C@@H](CC(O)=O)C(O)=O.O=C(C1=CN(CC)C2=C(C=C(F)C(N3CC(C)NCC3)=C2F)C1=O)O
Biological Activity: Lomefloxacin (SC47111A) aspartate is a broad-spectrum quinolone antibiotic, with antimicrobial activity. Lomefloxacin aspartate can be used for researching respiratory tract infections, genitourinary infections, gastrointestinal infections, ENT infections, etc.[1][2].
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Lomefloxacin (aspartate) | Lomefloxacin (SC47111A) aspartate is a broad-spectrum quinolone antibiotic, with antimicrobial activity. Lomefloxacin aspartate can be used for researching respiratory tract infections, genitourinary infections, gastrointestinal infections, ENT infections, etc.. | |||||||||||||||||||||
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References
- [1]. Hoogkamp-Korstanje JA. In-vitro activities of ciprofloxacin, levofloxacin, lomefloxacin, ofloxacin, pefloxacin, sparfloxacin and trovafloxacin against gram-positive and gram-negative pathogens from respiratory tract infections. J Antimicrob Chemother. 1997 Sep;40(3):427-31. [Content Brief]
- [2]. Reem I Al-Wabli. Lomefloxacin. Profiles Drug Subst Excip Relat Methodol. 2017;42:193-240. [Content Brief]
