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  3. Neomycin sulfate

Neomycin sulfate, an aminoglycoside antibiotic, exerts antibacterial activity through irreversible binding of the nuclear 30S ribosomal subunit, thereby blocking bacterial protein synthesis. Neomycin sulfate is a known phospholipase C (PLC) inhibitor. Neomycin sulfate potently inhibits both the nuclear translocation of angiogenin and angiogenin-induced cell proliferation and angiogenesis. Neomycin sulfate inhibits IP3-mediated Ca2+ release, MgATP-dependent Ca2+ uptake, and electrical excitation-evoked skeletal muscle Ca2+ transients. Neomycin sulfate depletes gut microbiota in specific mouse models, causes hearing impairment, and kidney damage with prolonged exposure. Neomycin sulfate can be used for the research of cancer.

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

CAS No. : 1405-10-3

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Customer Review

Based on 68 publication(s) in Google Scholar

Other Forms of Neomycin sulfate:

Top Publications Citing Use of Products

68 Publications Citing Use of MCE Neomycin sulfate

In Vivo Efficacy Study
PK/PD Analysis
Others
Bio/Physico-chemical Assay

    Neomycin sulfate purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2025 Apr;12(16):e2415041.  [Abstract]

    ABR thresholds in each group. The statistical differences were analyzed between Neomycin (100 mg/kg once daily for 14 days, ip) + PO group and Neomycin group.

    Neomycin sulfate purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2025 Apr;12(16):e2415041.  [Abstract]

    Effects of different levels of UA on HCs in the apical, middle, and basal turns after Neomycin (0.5 mM) treatment for 24 h.

    Neomycin sulfate purchased from MedChemExpress. Usage Cited in: Gut Microbes. 2023 Dec;15(2):2282790.  [Abstract]

    Depletion of CD8+ T cells in ABX-treated B16-F0 tumor-bearing mice dampened the antitumor effect of butyrate combined with anti-PD-1 (Figure 4b–e). Decreased serum IFN-γ and TNF-α production during the depletion of CD8+ T cells was also observed. ABX:an antibiotic cocktail of 0.5 g/L Vancomycin, 1 g/L Metronidazole, 1 g/L Neomycin and 1 g/L Ampicillin.

    Neomycin sulfate purchased from MedChemExpress. Usage Cited in: Gut Microbes. 2023 Dec;15(2):2249143.  [Abstract]

    Targeted metabolomics analysis of gut microbial metabolites (AA, PA, and BA) in colon contents (feces) and serum from mice with or without ABX treatment (n = 6 per group). ABX: an antibiotic cocktail of 0.5 g/L Vancomycin, 1 g/L Metronidazole,1 g/L Neomycin and 1 g/L Ampicillin
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Neomycin sulfate, an aminoglycoside antibiotic, exerts antibacterial activity through irreversible binding of the nuclear 30S ribosomal subunit, thereby blocking bacterial protein synthesis. Neomycin sulfate is a known phospholipase C (PLC) inhibitor. Neomycin sulfate potently inhibits both the nuclear translocation of angiogenin and angiogenin-induced cell proliferation and angiogenesis. Neomycin sulfate inhibits IP3-mediated Ca2+ release, MgATP-dependent Ca2+ uptake, and electrical excitation-evoked skeletal muscle Ca2+ transients. Neomycin sulfate depletes gut microbiota in specific mouse models, causes hearing impairment, and kidney damage with prolonged exposure. Neomycin sulfate can be used for the research of cancer[1][2].

    IC50 & Target

    Aminoglycoside

     

    In Vitro

    Neomycin sulfate (10-500 μM; 30 min) inhibits nuclear translocation of angiogenin in HUVE cells with 60% inhibition at 100 μM and residual 14% translocation at 500 μM[1].
    Neomycin sulfate (5-50 μM; 48 h) completely abolishes angiogenin-induced proliferation of HUVE cells at 50 μM, with 49% inhibition at 5 μM and 69% inhibition at 25 μM[1].
    Neomycin sulfate (5-50 μM; 2 h) does not inhibit the ribonucleolytic activity of angiogenin against yeast tRNA at concentrations up to 50 μM[1].
    Neomycin sulfate (0.25-1.25 mM; 6 minutes after cell permeabilization) inhibits IP3-mediated Ca2+ release in saponin-permeabilized RINmSF insulinoma cells in a dose-dependent manner and also inhibits the initial rate of net Ca2+ uptake into non-mitochondrial pools[2].
    Neomycin sulfate (1.25 mM) inhibits IP₃-mediated 45Ca2+ release from saponin-permeabilized rat hepatocytes, with greater inhibition at low IP₃ concentrations[2].
    Neomycin sulfate covalently linked to glass beads avidly binds IP3 (93% retention) and ATP (97-98% retention) and also binds PIP2 (70% retention), but binds IP1 and myo-inositol poorly[2].

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

    Cell Proliferation Assay[1]

    Cell Line: human umbilical vein endothelial (HUVE) cells
    Concentration: 5, 10, 25, 50 μM
    Incubation Time: 48 h
    Result: Inhibited angiogenin-induced proliferation in a dose-dependent, non-linear manner; reduced proliferation by 49% at 5 μM, by 69% at 25 μM, and completely abolished angiogenin-induced proliferation at 50 μM; did not affect basal proliferation or cell viability when used alone.
    In Vivo

    Neomycin sulfate (4-200 ng; applied to CAM; single dose) at 20 ng per egg completely inhibits angiogenin-induced angiogenesis in the chicken CAM model[1].
    Neomycin sulfate (1 g/L; p.o.; daily; 14 days) as part of a broad-spectrum antibiotic cocktail depletes over 90% of gut microbiota in 7.5-month-old APP/PS1 transgenic mice[3].

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

    Animal Model: SPAFAS (fertilized eggs)[1]
    Dosage: 4 ng; 20 ng; 200 ng
    Administration: applied to CAM; single dose
    Result: Decreased the percentage of angiogenin-induced positive angiogenesis from 55% to 40% with 4 ng; decreased it to 20% (equivalent to water control background) with 20 ng; decreased it to 25% with 200 ng.
    Animal Model: SPAFAS (fertilized eggs)[1]C57BL/6J APP/PS1 (7.5 months old; 6 female, 6 male; Alzheimer's disease transgenic model)[3]
    Dosage: 1 g/L (as part of broad-spectrum antibiotic cocktail)
    Administration: p.o.; daily; 14 days (in drinking water)
    Result: Achieved >90% depletion of gut microbiota.
    Molecular Weight

    908.88

    Formula

    C23H52N6O25S3

    CAS No.
    Appearance

    Solid

    Color

    White to light yellow

    SMILES

    O[C@H]1[C@H](O)[C@@H](N)[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]3O[C@H](CO)[C@@H](O[C@H]4O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]4N)[C@H]3O)O[C@@H]1CN.[3H2SO4]

    Structure Classification
    Initial Source

    Micromonospora species

    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 : 250 mg/mL (275.06 mM; Need ultrasonic)

    DMSO : < 1 mg/mL (insoluble or slightly soluble)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 1.1003 mL 5.5013 mL 11.0026 mL
    5 mM 0.2201 mL 1.1003 mL 2.2005 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.

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    In Vivo:

    For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  PBS

      Solubility: 50 mg/mL (55.01 mM); Clear solution; Need ultrasonic

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

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    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: 99.86%

    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
    H2O 1 mM 1.1003 mL 5.5013 mL 11.0026 mL 27.5064 mL
    5 mM 0.2201 mL 1.1003 mL 2.2005 mL 5.5013 mL
    10 mM 0.1100 mL 0.5501 mL 1.1003 mL 2.7506 mL
    15 mM 0.0734 mL 0.3668 mL 0.7335 mL 1.8338 mL
    20 mM 0.0550 mL 0.2751 mL 0.5501 mL 1.3753 mL
    25 mM 0.0440 mL 0.2201 mL 0.4401 mL 1.1003 mL
    30 mM 0.0367 mL 0.1834 mL 0.3668 mL 0.9169 mL
    40 mM 0.0275 mL 0.1375 mL 0.2751 mL 0.6877 mL
    50 mM 0.0220 mL 0.1100 mL 0.2201 mL 0.5501 mL
    60 mM 0.0183 mL 0.0917 mL 0.1834 mL 0.4584 mL
    80 mM 0.0138 mL 0.0688 mL 0.1375 mL 0.3438 mL
    100 mM 0.0110 mL 0.0550 mL 0.1100 mL 0.2751 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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