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Levofloxacin (hydrochloride)

CAT: 0804-HY-B0330B-01Size: 1 gDry Ice: NoHazardous: No
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CAT#:0804-HY-B0330B-01Size:1 g
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Description
Levofloxacin hydrochloride is an orally active antibiotic. Levofloxacin inhibits DNA gyrase and topoisomerase IV activity, inducing Apoptosis. Levofloxacin hydrochloride has antibacterial activity against both Gram-positive and Gram-negative bacteria. Levofloxacin hydrochloride exhibits anticancer activity against lung cancer. Levofloxacin hydrochloride has anti-acnegenic, anxiogenic, and analgesic effects. Levofloxacin hydrochloride shortens sleep duration in mice. Levofloxacin hydrochloride can be used in the research of infectious diseases (such as tuberculosis, chronic periodontitis, bacterial infections associated with stable COPD, and BK viremia) and lung cancer[1][2][3][4][5][6][7][8][9][10].
CAS Number
177325-13-2
Product Name Alternative
(-) -Ofloxacin (hydrochloride)
UNSPSC
12352005
Hazard Statement
H302, H317, H334, H361, H362
Target
Antibiotic; Apoptosis; Bacterial; DNA/RNA Synthesis; Orthopoxvirus; Topoisomerase
Type
Reference compound
Related Pathways
Anti-infection; Apoptosis; Cell Cycle/DNA Damage
Applications
COVID-19-anti-virus
Field of Research
Cancer; Infection; Neurological Disease
Assay Protocol
https://www.medchemexpress.com/levofloxacin-hydrochloride.html
Purity
98.0
Solubility
H2O : 20 mg/mL (ultrasonic; warming; heat to 60°C)
Smiles
[H]Cl.O=C(C(C1=O)=CN2[C@@H](C)COC3=C(N4CCN(C)CC4)C(F)=CC1=C23)O
Molecular Formula
C18H21ClFN3O4
Molecular Weight
397.83
Precautions
H302, H317, H334, H361, H362
References & Citations
[1]Drlica K, et al. DNA gyrase, topoisomerase IV, and the 4-quinolones. Microbiol Mol Biol Rev. 1997 Sep;61 (3) :377-92.|[2]Smee DF, et al. A review of compounds exhibiting anti-orthopoxvirus activity in animal models. Antiviral Res. 2003 Jan;57 (1-2) :41-52.|[3]Rand A, et al. Effect of levofloxacin on some body tissues in mice. Effect of levofloxacin on some body tissues in mice. Iraqi Journal of Veterinary Sciences, 2021. |[4]JI B, et al. In vitro and in vivo activities of levofloxacin against Mycobacterium tuberculosis. Antimicrob Agents Chemother. 1995 Jun;39 (6) :1341-4. |[5]Siva R, et al. Effect of levofloxacin on neutrophilic airway inflammation in stable COPD: a randomized, double-blind, placebo-controlled trial. Int J Chron Obstruct Pulmon Dis. 2014 Feb 7;9:179-86.|[6]Pradeep AR, et al. Clinical and microbiological effects of levofloxacin in the treatment of chronic periodontitis: a randomized, placebo-controlled clinical trial. J Investig Clin Dent. 2015 Aug;6 (3) :170-8. |[7]Lee BT, et al. Efficacy of levofloxacin in the treatment of BK viremia: a multicenter, double-blinded, randomized, placebo-controlled trial. Clin J Am Soc Nephrol. 2014 Mar;9 (3) :583-9. |[8]Ishida H, et al. In vitro and in vivo activities of levofloxacin against biofilm-producing Pseudomonas aeruginosa. Antimicrob Agents Chemother. 1998 Jul;42 (7) :1641-5. |[9]Song M, et al. Antibiotic drug levofloxacin inhibits proliferation and induces apoptosis of lung cancer cells through inducing mitochondrial dysfunction and oxidative damage. Biomed Pharmacother. 2016 Dec;84:1137-1143. |[10]Erden BF, et al. Antidepressant, anxiogenic, and antinociceptive properties of levofloxacin in rats and mice. Pharmacol Biochem Behav. 2001 Mar;68 (3) :435-41.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
Topoisomerase
Citation 01
Emerg Microbes Infect. 2024 Dec;13 (1) :2321981.|J Med Virol. 2025 Oct;97 (10) :e70655.|ACS Infect Dis. 2024 Apr 12;10 (4) :1327-1338.|Acta Pharm Sin B. 2025 Sep 19.|AMB Express. 2024 Dec 24;14 (1) :141.|Antibiotics (Basel) . 2022 Feb 1;11 (2) :192.|Antimicrob Agents Chemother. 2021 Feb 17;65 (3) :e01921-20.|bioRxiv. 2024 May 10.|bioRxiv. 2025 January 19.|Cell Rep Methods. 2023 Oct 23;3 (10) :100599.|Chin J Traumatol. 2024 Jul 3:S1008-1275 (24) 00075-0.|Clin Chem. 2019 Dec;65 (12) :1522-1531. |Commun Biol. 2025 Oct 6;8 (1) :1425.|Diagn Microbiol Infect Dis. 2025 Nov 4;114 (2) :117181.|EBioMedicine. 2025 May 30:117:105776.|Eur J Clin Microbiol Infect Dis. 2025 Sep 29.|Future Microbiol. 2025 Oct 13:1-10.|Infect Genet Evol. 2025 Sep:133:105780.|Int J Antimicrob Agents. 2025 Jun 9:107551.|Microbiol Spectr. 2025 May 19:e0307424.|Microbiol Spectr. 2025 Oct 15:e0122125.|Nat Commun. 2025 May 10;16 (1) :4366.|PLoS One. 2024 Apr 18;19 (4) :e0298577.|Res Sq. 2025 Aug 05.|Results Chem. 2024 Oct.|SSRN. 2025 Oct 14.|Toxics. 2025 Feb 5;13 (2) :122.|Water. 2025 Jun 6.|Nat Commun. 2022 Mar 2;13 (1) :1116.

Chemical Information

Levofloxacin hydrochloride
CAS Number177325-13-2
PubChem CID9908810
IUPAC Name(2S)-7-fluoro-2-methyl-6-(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;hydrochloride
Molecular FormulaC18H21ClFN3O4
Molecular Weight397.8
Topological Polar Surface Area73.3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count8
Rotatable Bond Count2
Heavy Atom Count27
Formal Charge0
Complexity634
SMILES
C[C@H]1COC2=C3N1C=C(C(=O)C3=CC(=C2N4CCN(CC4)C)F)C(=O)O.Cl
InChI
InChI=1S/C18H20FN3O4.ClH/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21;/h7-8,10H,3-6,9H2,1-2H3,(H,24,25);1H/t10-;/m0./s1
InChIKey
CAOOISJXWZMLBN-PPHPATTJSA-N
Chemical Structure
2D Structure
2D structure of Levofloxacin hydrochloride
CAS: 177325-13-2
CID: 9908810
Formula: C18H21ClFN3O4
MW: 397.8
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight397.8
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count8
Rotatable Bond Count2
Exact Mass397.1204620
Monoisotopic Mass397.1204620
Topological Polar Surface Area73.3 Ų
Heavy Atom Count27
Formal Charge0
Complexity634
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count2
Compound Is CanonicalizedYes