Levofloxacin-d8 (hydrochloride)

Levofloxacin-d8 (hydrochloride) Suppliers list
Company Name: CHINA ISOTOPE CO., LIMITED  
Tel: 02151600108 13062666369
Email: info@isotopechem.com
Company Name: Shanghai Yifei Biotechnology Co. , Ltd.  
Tel: 021-65675885 18964387627
Email: customer_service@efebio.com
Company Name: Nanjing Shizhou Biology Technology Co.,Ltd  
Tel: 17301488900
Email: judy.xia@synzest.com
Company Name: TLC Pharmaceutical Standards Ltd.  
Tel: 18012923235
Email: chinasales04@tlcstandards.com.cn
Company Name: Zhejiang Huida Biotech Co., Ltd.  
Tel: 0571-89903022 18679456698
Email: zilong@hizyme.com
Levofloxacin-d8 (hydrochloride) Basic information
Product Name:Levofloxacin-d8 (hydrochloride)
Synonyms:(2S)-7-fluoro-2-methyl-6-(2,2,3,3,5,5,6,6-octadeuterio-4-methylpiperazin-1-yl)-10-oxo-4-oxa-1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8,11-tetraene-11-carboxylic acid
CAS:2699607-50-4
MF:C18H12D8FN3O4.ClH
MW:405.88
EINECS:
Product Categories:
Mol File:2699607-50-4.mol
Levofloxacin-d8 (hydrochloride) Structure
Levofloxacin-d8 (hydrochloride) Chemical Properties
solubility DMSO: soluble
form A solid
color White to off-white
Safety Information
MSDS Information
Levofloxacin-d8 (hydrochloride) Usage And Synthesis
DescriptionLevofloxacin-d8 is intended for use as an internal standard for the quantification of levofloxacin by GC- or LC-MS. Levofloxacin is a fluoroquinolone antibiotic and the active stereoisomer of ofloxacin .1 It is active against S. aureus, S. epidermidis, B. subtilis, E. coli, P. aeruginosa, and K. pneumoniae (MICs = 0.25, 0.25, 0.5, 0.03, 4, and 0.25 μg/ml, respectively).2 Levofloxacin inhibits S. aureus DNA gyrase and topoisomerase IV (IC50s = 8.06 and 9.81 μg/ml, respectively).3 It eliminates infection in rat models of endocarditis caused by methicillin-sensitive or -resistant S. aureus.4 Formulations containing levofloxacin have been used in the treatment of various bacterial infections.
UsesLevofloxacin-d8 (hydrochloride) is deuterium labeled Levofloxacin (hydrochloride).
References1. Norrby, S.R. Levofloxacin Expert Opin. Pharmacother. 1(1),109-119(1999).
2. Mohammadhosseini, N., Alipanahi, Z., Alipour, E., et al. Synthesis and antibacterial activity of novel levofloxacin derivatives containing a substituted thienylethyl moiety. Daru. 20(1),(2012).
3. Takei, M., Fukuda, H., Kishii, R., et al. Target preference of 15 quinolones against Staphylococcus aureus, based on antibacterial activities and target inhibition Antimicrob. Agents Chemother. 45(12),3544-3547(2001).
4. Entenza, J.M., Vouillamoz, J., Glauser, M.P., et al. Levofloxacin versus ciprofloxacin, flucloxacillin, or vancomycin for treatment of experimental endocarditis due to methicillin-susceptible or -resistant Staphylococcus aureus Antimicrob. Agents Chemother. 41(8),1662-1667(1997).
Levofloxacin-d8 (hydrochloride) Preparation Products And Raw materials
Tag:Levofloxacin-d8 (hydrochloride)(2699607-50-4) Related Product Information
Levofloxacin heMihydrate Sarafloxacin-d8 Hydrochloride Marbofloxacin-d8 (hydrochloride) Ciprofloxacin-D8 hydrochloride hydrate (see Data Sheet) Chlorhexidine-d8 HCl