Lomefloxacin-d5 hydrochloride

For research use only. Not for therapeutic Use.

  • CAT Number: S000216
  • Molecular Formula: C17H15D5ClF2N3O3
  • Molecular Weight: 392.84
  • Purity: ≥95%
Inquiry Now

Lomefloxacin-d5 hydrochloride, a premium pharmaceutical research compound designed for advanced antibacterial and antimicrobial studies. As a deuterated analog of Lomefloxacin, it offers enhanced stability and improved pharmacokinetic properties. Lomefloxacin-d5 hydrochloride is ideal for use in pharmacological and biochemical research, providing precise and reliable data for your studies. This high-purity compound ensures consistent results, aiding in the development of novel antibacterial therapies. Trusted by leading laboratories, Lomefloxacin-d5 hydrochloride is your go-to solution for cutting-edge antibacterial research. Unlock new possibilities in infection treatment with Lomefloxacin-d5 hydrochloride, where innovation meets reliability.


Catalog Number S000216
Molecular Formula C17H15D5ClF2N3O3
Purity ≥95%
IUPAC Name 6,8-difluoro-7-(3-methylpiperazin-1-yl)-4-oxo-1-(1,1,2,2,2-pentadeuterioethyl)quinoline-3-carboxylic acid;hydrochloride
InChI InChI=1S/C17H19F2N3O3.ClH/c1-3-21-8-11(17(24)25)16(23)10-6-12(18)15(13(19)14(10)21)22-5-4-20-9(2)7-22;/h6,8-9,20H,3-5,7H2,1-2H3,(H,24,25);1H/i1D3,3D2;
InChIKey KXEBLAPZMOQCKO-IYSLTCQOSA-N
SMILES [2H]C([2H])([2H])C([2H])([2H])N1C=C(C(=O)C2=CC(=C(C(=C21)F)N3CCNC(C3)C)F)C(=O)O.Cl
Reference

[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]

[3]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-223.
[Content Brief]

Request a Quote