1. Anti-infection Cell Cycle/DNA Damage Apoptosis
  2. Antibiotic Bacterial DNA/RNA Synthesis Topoisomerase Orthopoxvirus Apoptosis
  3. Levofloxacin hydrochloride

Levofloxacin hydrochloride  (Synonyms: (-)-Ofloxacin hydrochloride)

Cat. No.: HY-B0330B Purity: 99.99%
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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.

For research use only. We do not sell to patients.

CAS No. : 177325-13-2

Size Price Stock Quantity
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in Water
ready for reconstitution
In-stock
Solution
10 mM * 1 mL in Water In-stock
Solid
1 g In-stock
5 g In-stock
10 g In-stock
50 g   Get quote  

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This product is a controlled substance and not for sale in your territory.

Customer Review

Based on 35 publication(s) in Google Scholar

Other Forms of Levofloxacin hydrochloride:

Top Publications Citing Use of Products

35 Publications Citing Use of MCE Levofloxacin hydrochloride

Microbiological Assay
Cell Proliferation/Viability Assay

    Levofloxacin hydrochloride purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 May 10;16(1):4366.  [Abstract]

    M. bovis BCG Russia WT in LFX (0-25 h) 1 mg/L.

    Levofloxacin hydrochloride purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 May 10;16(1):4366.  [Abstract]

    M. bovisBCG Russia FQR in LFX (0-25 h) 1 mg/L.

    Levofloxacin hydrochloride purchased from MedChemExpress. Usage Cited in: Acta Pharm Sin B. 2025 Dec;15(12):6382-6398.

    Levofloxacin exhibited toxicity at 25 × Cmax, which resulted in a 65% reduction in organoid cell viability.

    Levofloxacin hydrochloride purchased from MedChemExpress. Usage Cited in: EBioMedicine. 2025 May 30:117:105776.  [Abstract]

    Killing curves of different Ms rpoB mutants after exposure to LFX (0-48 h) at 1 μg/mL (5 × MIC) in 7H9 medium.

    Levofloxacin hydrochloride purchased from MedChemExpress. Usage Cited in: Antibiotics (Basel). 2022 Feb 1;11(2):192.

    Determined minimum inhibitory concentrations (MICs) of Gepotidacin, Levofloxacin, Moxifloxacin, and Co-trimoxazole against S. maltophilia.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    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].

    IC50 & Target

    TOPO IV

     

    In Vitro

    Levofloxacin hydrochloride inhibits the growth of 18 drug-susceptible Mycobacterium tuberculosis strains with MICs ranging from 0.25 to 1.0 μg/mL and a MIC50 of 0.5 μg/mL[4].
    Levofloxacin (24 h) hydrochloride exhibits strong bactericidal activity against biofilm-forming sessile cells of Pseudomonas aeruginosa[8].
    Levofloxacin (50-200 μg/mL; 24-72 h) hydrochloride inhibits proliferation and induces apoptosis of lung cancer cells (A549, H3255, NCL-69, H460) through inducing mitochondrial dysfunction and oxidative damage[9].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    In Vivo

    Levofloxacin (10.7 mg/kg; i.p., once daily for 10 days or 3 weeks) hydrochloride time-dependently induces toxic effects on liver and heart in albino mice[3].
    Levofloxacin (50-300 mg/kg; p.o. via esophageal cannula; six times weekly; 4 weeks) hydrochloride exerts dose-dependent anti-Mycobacterium tuberculosis activity in female outbred Swiss mice[4].
    Levofloxacin (10-40 mg/kg, i.p.) hydrochloride exerts anxiogenic-like effect in rats and shortens Pentobarbital-induced sleeping time, exhibits analgesic activity in mice[10].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Animal Model: Matured male Albino mice[3]
    Dosage: 10.7 mg/kg
    Administration: Intraperitoneal injection; 10.7 mg/kg, once daily for 10 days or 3 weeks.
    Result: Induced severe congestion of blood vessels in the portal area, central veins with inflammatory cells infiltration, necrosis with pyknosis of cardiac muscle nuclei and apoptosis, degeneration and necrosis of hepatocytes.
    Molecular Weight

    397.83

    Formula

    C18H21ClFN3O4

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    [H]Cl.O=C(C(C1=O)=CN2[C@@H](C)COC3=C(N4CCN(C)CC4)C(F)=CC1=C23)O

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    4°C, sealed storage, away from moisture

    *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

    Solvent & Solubility
    In Vitro: 

    H2O : ≥ 100 mg/mL (251.36 mM)

    DMSO : 5.83 mg/mL (14.65 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    *"≥" means soluble, but saturation unknown.

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 2.5136 mL 12.5682 mL 25.1364 mL
    5 mM 0.5027 mL 2.5136 mL 5.0273 mL
    View the Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

    • Molarity Calculator

    • Dilution Calculator

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

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    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

    Dosage

    mg/kg

    Animal weight
    (per animal)

    g

    Dosing volume
    (per animal)

    μL

    Number of animals

    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Calculation results:
    Working solution concentration: mg/mL
    This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
    The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).
    Purity & Documentation

    Purity: 99.99%

    References

    Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO / H2O 1 mM 2.5136 mL 12.5682 mL 25.1364 mL 62.8409 mL
    5 mM 0.5027 mL 2.5136 mL 5.0273 mL 12.5682 mL
    10 mM 0.2514 mL 1.2568 mL 2.5136 mL 6.2841 mL
    H2O 15 mM 0.1676 mL 0.8379 mL 1.6758 mL 4.1894 mL
    20 mM 0.1257 mL 0.6284 mL 1.2568 mL 3.1420 mL
    25 mM 0.1005 mL 0.5027 mL 1.0055 mL 2.5136 mL
    30 mM 0.0838 mL 0.4189 mL 0.8379 mL 2.0947 mL
    40 mM 0.0628 mL 0.3142 mL 0.6284 mL 1.5710 mL
    50 mM 0.0503 mL 0.2514 mL 0.5027 mL 1.2568 mL
    60 mM 0.0419 mL 0.2095 mL 0.4189 mL 1.0473 mL
    80 mM 0.0314 mL 0.1571 mL 0.3142 mL 0.7855 mL
    100 mM 0.0251 mL 0.1257 mL 0.2514 mL 0.6284 mL

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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