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RG7834  (Synonyms: RO 7020322; (S)-RO0321)

Cat. No.: HY-117650A Purity: 99.29%
Handling Instructions Technical Support

RG7834 (RO 7020322) is a highly selective and orally bioavailable HBV inhibitor, potently inhibits HBV antigens (both HBsAg and HBeAg) and HBV DNA, with IC50s of 2.8, 2.6, and 3.2 nM, respectively, in dHepaRG Cells.

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

CAS No. : 2072057-17-9

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10 mM * 1 mL in DMSO
ready for reconstitution
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Customer Review

Based on 9 publication(s) in Google Scholar

Other Forms of RG7834:

Top Publications Citing Use of Products

    RG7834 purchased from MedChemExpress. Usage Cited in: J Virol. 2025 Oct 10:e0092225.  [Abstract]

    Activation of HBV-RADARS corresponds to its target HBV RNA levels in HepG2.2.15. The results showed that treating cells with the HBV RNA destabilizing compound RG7834 (1 μM) (except for HBx mRNA) significantly reduced total HBV RNA and antigen expression, corresponding with a decrease in HBV RNA-mediated Gluc activation from the HBV-RADARS reporter.

    RG7834 purchased from MedChemExpress. Usage Cited in: Proc Natl Acad Sci U S A. 2024 Jun 4;121(23):e2316734121.  [Abstract]

    TENT4 inhibitor, RG7834 (1 μM; 1 h), impairs liquid-to-solid phase transition of Amyloid bodies. Numbers denote percentage of cells with intranucleolar foci.

    RG7834 purchased from MedChemExpress. Usage Cited in: Research Square Preprint. 2022 May.

    Telomere lengths determined by Southern blot TRF analysis of gDNA prepared from WT_iPSC_F and R449G_iPSC_1 treated with RG7834 (1 μM), Cordycepin, or DMSO. The results showed that RG7834 partially restored telomere length in R449G_iPSC_1 (lanes 7).

    RG7834 purchased from MedChemExpress. Usage Cited in: Research Square Preprint. 2022 May.

    Total RNA prepared from WT_iPSC_F and R449G_iPSC_1 cells treated with RG7834 (1 μM), Cordycepin, or DMSO was subjected to qRT–PCR for oligoadenylated hTR. Bar graph of the mean fold change relative to DMSO-treated samples and normalized to GAPDH, ATP5b, and HPRT. The results showed that RG7834 (1 μM) led to a decrease in the proportion of oligoadenylated hTR.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    RG7834 (RO 7020322) is a highly selective and orally bioavailable HBV inhibitor, potently inhibits HBV antigens (both HBsAg and HBeAg) and HBV DNA, with IC50s of 2.8, 2.6, and 3.2 nM, respectively, in dHepaRG Cells[1].

    IC50 & Target

    IC50: 2.8 nM (HBsAg), 2.6 nM (HBeAg), 3.2 nM (HBV DNA)[1]

    Cellular Effect
    Cell Line Type Value Description References
    HepG2 2.2.15 CC50
    > 10 μM
    Compound: 1; RG-7834
    Cytotoxicity against human HepG2.2.15 cells assessed as reduction in cell viability measured after 4 days by CellTiter-Glo reagent based assay
    Cytotoxicity against human HepG2.2.15 cells assessed as reduction in cell viability measured after 4 days by CellTiter-Glo reagent based assay
    [PMID: 34267883]
    HepG2 2.2.15 CC50
    > 50 μM
    Compound: (S)-64; RG7834
    Cytotoxicity against human HepG2.2.15 cells by CCK-8 assay
    Cytotoxicity against human HepG2.2.15 cells by CCK-8 assay
    [PMID: 30286292]
    HepG2 2.2.15 EC50
    1.2 nM
    Compound: RG7834
    Antiviral activity against HBV infected in human HepG2.2.15 cells assessed as inhibition of HBsAg level incubated for 6 days by microplate-based chemiluminescence immunoassay
    Antiviral activity against HBV infected in human HepG2.2.15 cells assessed as inhibition of HBsAg level incubated for 6 days by microplate-based chemiluminescence immunoassay
    [PMID: 38190324]
    HepG2 2.2.15 IC50
    0.001 μM
    Compound: 1; RG7834
    Inhibition HBsAg secretion in human HepG2.2.15 cells treated for 3 days followed by medium replacement without compound measured after 2 days by CLIA
    Inhibition HBsAg secretion in human HepG2.2.15 cells treated for 3 days followed by medium replacement without compound measured after 2 days by CLIA
    [PMID: 38428537]
    In Vitro

    RG7834 ((S)-(+)-64) is a highly selective and orally bioavailable HBV inhibitor, potently inhibits HBV antigens (both HBsAg and HBeAg) and HBV DNA, with IC50s of 2.8, 2.6, and 3.2 nM, respectively, in dHepaRG Cells[1].
    RG7834 has no activity against CYP3A4, CYP2D6, CYP2C9 (IC50s >50 μM) or hERG channel[1].

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

    In Vivo

    RG7834 (4 mg/kg, twice daily for 21 days) shows anti-HBV efficacy in HBV-infected human liver chimeric uPA-SCID mice[1].
    RG7834 (2, 14.5 mg/kg, p.o.) exhibits good oral bioavail ability, with a half-life of 4.9 h in mice[1].

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

    Animal Model: HBV-infected human liver chimeric uPA-SCID mice[1]
    Dosage: 4 mg/kg
    Administration: Twice daily for 21 days
    Result: Reduced both HBsAg and HBeAg, also decreased serum HBV DNA by 0.6 log10 in mice.
    Clinical Trial
    Molecular Weight

    401.45

    Formula

    C22H27NO6

    CAS No.
    Appearance

    Solid

    Color

    Light yellow to yellow

    SMILES

    O=C(O)C1=CN2[C@@H](CC3=CC(OCCCOC)=C(C=C3C2=CC1=O)OC)C(C)C

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 2 years
    -20°C 1 year
    Solvent & Solubility
    In Vitro: 

    DMSO : 125 mg/mL (311.37 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 2.4910 mL 12.4549 mL 24.9097 mL
    5 mM 0.4982 mL 2.4910 mL 4.9819 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

    • 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

    Concentration (start)

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    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:  5% DMSO    95% (20% SBE-β-CD in Saline)

      Solubility: ≥ 2.87 mg/mL (7.15 mM); Clear solution

    • Protocol 2

      Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.08 mg/mL (5.18 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 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.
    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.
    Please enter your animal formula composition:
    %
    DMSO +
    +
    %
    Tween-80 +
    %
    Saline
    Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
    The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
    Calculation results:
    Working solution concentration: mg/mL
    Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).
    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).
    Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
     If the continuous dosing period exceeds half a month, please choose this protocol carefully.
    Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
    Purity & Documentation

    Purity: 99.29%

    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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 2.4910 mL 12.4549 mL 24.9097 mL 62.2743 mL
    5 mM 0.4982 mL 2.4910 mL 4.9819 mL 12.4549 mL
    10 mM 0.2491 mL 1.2455 mL 2.4910 mL 6.2274 mL
    15 mM 0.1661 mL 0.8303 mL 1.6606 mL 4.1516 mL
    20 mM 0.1245 mL 0.6227 mL 1.2455 mL 3.1137 mL
    25 mM 0.0996 mL 0.4982 mL 0.9964 mL 2.4910 mL
    30 mM 0.0830 mL 0.4152 mL 0.8303 mL 2.0758 mL
    40 mM 0.0623 mL 0.3114 mL 0.6227 mL 1.5569 mL
    50 mM 0.0498 mL 0.2491 mL 0.4982 mL 1.2455 mL
    60 mM 0.0415 mL 0.2076 mL 0.4152 mL 1.0379 mL
    80 mM 0.0311 mL 0.1557 mL 0.3114 mL 0.7784 mL
    100 mM 0.0249 mL 0.1245 mL 0.2491 mL 0.6227 mL
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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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