1. Neuronal Signaling
  2. Glucosylceramide Synthase (GCS)
  3. Miglustat hydrochloride

Miglustat hydrochloride  (Synonyms: N-Butyldeoxynojirimycin hydrochloride; NB-DNJ hydrochloride; OGT 918 hydrochloride)

Art. -Nr.: HY-17020A Reinheit: 99.97%
Handling Instructions Technical Support

Miglustat (N-Butyldeoxynojirimycin) hydrochloride is an orally active and reversible ceramide glucosyltransferase inhibitor, with blood-brain barrier permeability. Miglustat hydrochloride can be used for the research of type I gaucher disease.

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CAS. Nr. : 210110-90-0

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10 mM * 1 mL in DMSO
ready for reconstitution
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Based on 6 publication(s) in Google Scholar

Other Forms of Miglustat hydrochloride:

Top Publications Citing Use of Products

    Miglustat hydrochloride purchased from MedChemExpress. Usage Cited in: J Virol. 2025 Mar 18;99(3):e0001825.  [Abstract]

    Miglustat (5, 10 μM; 24 h) showed no cytotoxicity for Vero cells.

    Miglustat hydrochloride purchased from MedChemExpress. Usage Cited in: J Virol. 2025 Mar 18;99(3):e0001825.  [Abstract]

    Miglustat (5, 10 μM) decreased the PEDV N mRNA levels in a dose-dependent manner in Vero cells.

    Miglustat hydrochloride purchased from MedChemExpress. Usage Cited in: J Virol. 2025 Mar 18;99(3):e0001825.  [Abstract]

    Miglustat (5, 10 μM) decreased the PEDV N prodein levels in a dose-dependent manner in Vero cells.

    Miglustat hydrochloride purchased from MedChemExpress. Usage Cited in: J Virol. 2025 Mar 18;99(3):e0001825.  [Abstract]

    Immunofluorescence assay (IFA) images of Vero cells infected with PEDV and treated with indicated Miglustat (5, 10 μM). Viral N-protein is shown in green, and the nuclei are blue.

    Miglustat hydrochloride purchased from MedChemExpress. Usage Cited in: Nat Commun. 2024 Aug 14;15(1):6970.  [Abstract]

    Miglustat combined with anti-PD-1 promotes tumour inhibition. MC38-OVA cells (1 × 105 328 ) were subcutaneously injected into C57BL/6 mice treated with PBS, Miglustat alone (10 mg/kg), anti-PD-1 antibody alone (200 mg/kg per mouse) or Miglustat plus anti-PD-1 as indicated and tumour formation was observed. Tumour sizes were measured every 3 days. The average and individual tumour curves are shown.

    Miglustat hydrochloride purchased from MedChemExpress. Usage Cited in: Cell Rep. 2022 Jul 5;40(1):111049.  [Abstract]

    Ccin-EGFP-KI male mice were fed by 15 mg/kg Miglustat (NB-DNJ) per day for 5 weeks. NB-DNJ is a drug to disrupt the fusion of the small proacrosomal vesicles into a single acrosome. PNA-FITC-labeled acrosome and EGFP signals were almost lost after NB-DNJ treatment.

    Miglustat hydrochloride purchased from MedChemExpress. Usage Cited in: Cell Rep. 2022 Jul 5;40(1):111049.  [Abstract]

    Ccin-EGFP-KI male mice were fed by 15 mg/kg Miglustat (NB-DNJ) per day for 5 weeks, the shape of sperm from Ccin-eGFP-KI mice was obviously changed and the acrosome was absent.

    Miglustat hydrochloride purchased from MedChemExpress. Usage Cited in: Cell Rep. 2022 Jul 5;40(1):111049.  [Abstract]

    Ccin-EGFP-KI male mice were fed by 15 mg/kg Miglustat (NB-DNJ) per day for 5 weeks, The protein levels of Zpbp1 (an acrosomal marker) and eGFP-tagged calicin were significantly reduced.
    • Biologische Aktivität

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    Beschreibung

    Miglustat (N-Butyldeoxynojirimycin) hydrochloride is an orally active and reversible ceramide glucosyltransferase inhibitor, with blood-brain barrier permeability. Miglustat hydrochloride can be used for the research of type I gaucher disease[1][2][3].

    In Vitro

    Miglustat (200 μM; 2, 4 and 24 h) hydrochloride restores F508del-CFTR (cystic fibrosis transmembrane conductance regulator) function in cystic fibrosis (CF) bronchial epithelial IB3-1 and CuFi-1 cells. Miglustat hydrochloride reduces the inflammatory response to P. aeruginosa in both CF and non-CF bronchial cells[1].

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

    In Vivo

    Miglustat (0.2?mg/kg; oral administration; once) hydrochloride is able to rescue synaptic plasticity deficits, to restore ERKs activation and to counteract hyperexcitability[2].

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

    Animal Model: NPC1−/− mice[1]
    Dosage: 0.2 mg/kg
    Administration: Oral administration; once
    Result: Was able to rescue synaptic plasticity deficits, to restore ERKs activation and to counteract hyperexcitability.
    Molekulargewicht

    255.74

    Formel

    C10H22ClNO4

    CAS. Nr.
    Appearance

    Solid

    Color

    White to light brown

    SMILES

    O[C@H]1[C@H](O)[C@@H](CO)N(CCCC)C[C@@H]1O.[H]Cl

    Versand

    Room temperature in continental US; may vary elsewhere.

    Speicherung

    -20°C, stored under nitrogen

    *In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

    Lösungsmittel & Löslichkeit
    In Vitro: 

    DMSO : 65 mg/mL (254.16 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    H2O : ≥ 34 mg/mL (132.95 mM)

    *"≥" means soluble, but saturation unknown.

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 3.9102 mL 19.5511 mL 39.1022 mL
    5 mM 0.7820 mL 3.9102 mL 7.8204 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 (stored under nitrogen). 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.

    • Molaritätsrechner

    • Verdünnungsrechner

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

    Mass
    =
    Concentration
    ×
    Volume
    ×
    Molecular Weight *

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

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

    C1

    ×
    Volume (start)

    V1

    =
    Concentration (final)

    C2

    ×
    Volume (final)

    V2

    In Vivo:

    Select the appropriate dissolution method based on your experimental animal and administration route.

    For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
    To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
    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:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 3.25 mg/mL (12.71 mM); Clear solution

      This protocol yields a clear solution of ≥ 3.25 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (32.5 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

      Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
    • Protocol 2

      Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

      Solubility: ≥ 3.25 mg/mL (12.71 mM); Clear solution

      This protocol yields a clear solution of ≥ 3.25 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (32.5 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

      Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.

    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: 100 mg/mL (391.02 mM); Clear solution; Need ultrasonic

    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).
    Reinheit & Dokumentation

    Purity: 99.97%

    Verweise

    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 (stored under nitrogen). 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 / DMSO 1 mM 3.9102 mL 19.5511 mL 39.1022 mL 97.7555 mL
    5 mM 0.7820 mL 3.9102 mL 7.8204 mL 19.5511 mL
    10 mM 0.3910 mL 1.9551 mL 3.9102 mL 9.7756 mL
    15 mM 0.2607 mL 1.3034 mL 2.6068 mL 6.5170 mL
    20 mM 0.1955 mL 0.9776 mL 1.9551 mL 4.8878 mL
    25 mM 0.1564 mL 0.7820 mL 1.5641 mL 3.9102 mL
    30 mM 0.1303 mL 0.6517 mL 1.3034 mL 3.2585 mL
    40 mM 0.0978 mL 0.4888 mL 0.9776 mL 2.4439 mL
    50 mM 0.0782 mL 0.3910 mL 0.7820 mL 1.9551 mL
    60 mM 0.0652 mL 0.3259 mL 0.6517 mL 1.6293 mL
    80 mM 0.0489 mL 0.2444 mL 0.4888 mL 1.2219 mL
    100 mM 0.0391 mL 0.1955 mL 0.3910 mL 0.9776 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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    Produktname:
    Miglustat hydrochloride
    Art. -Nr.:
    HY-17020A
    Menge:
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