1. Apoptosis Autophagy
  2. MDM-2/p53 Autophagy Apoptosis Ferroptosis
  3. Eprenetapopt

Eprenetapopt  (Synonyms: APR-246; PRIMA-1Met)

Cat. No.: HY-19980 Purity: 99.52%
Handling Instructions Technical Support

Eprenetapopt (APR-246) is a first-in-class, small molecule that restores wild-type p53 functions in TP53-mutant cells. Eprenetapopt triggers apoptosis in tumor cells. Eprenetapopt also targets the selenoprotein thioredoxin reductase 1 (TrxR1), a key regulator of cellular redox balance.

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CAS No. : 5291-32-7

사이즈 가격 재고 수량
무료 샘플 (0.1 - 0.2 mg)   지금 신청하기  
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
해외재고보유
Solution
10 mM * 1 mL in DMSO 해외재고보유
Solid
5 mg 해외재고보유
10 mg 해외재고보유
25 mg 해외재고보유
50 mg 해외재고보유
100 mg 해외재고보유
200 mg   견적 받기  
500 mg   견적 받기  

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

고객리뷰

Based on 12 publication(s) in Google Scholar

Other Forms of Eprenetapopt:

Top Publications Citing Use of Products

    Eprenetapopt purchased from MedChemExpress. Usage Cited in: Clin Cancer Res. 2025 Jul 8.  [Abstract]

    A PCR assay was used to assess the influence of Eprenetapopt (APR-246; 20 µmol/L, 24 hours) on UBE2T mRNA levels in SG2 and GBM22 cells.

    Eprenetapopt purchased from MedChemExpress. Usage Cited in: Clin Cancer Res. 2025 Jul 8.  [Abstract]

    Western blot analysis was conducted to examine the impact of Eprenetapopt (APR-246; 20 µmol/L, 24 hours) on UBE2T protein levels.

    Eprenetapopt purchased from MedChemExpress. Usage Cited in: Clin Cancer Res. 2025 Jul 8.  [Abstract]

    In vivo bioluminescence experiments were conducted using orthotopic xenograft models of human glioma cells (SG2) in nude mice. On the first, third, fifth, and seventh days following the initial imaging session, Eprenetapopt (APR-246) was administered via i.p. injection at a dose of 400 mg/kg. The results indicated that APR-246 treatment inhibited the proliferation of SG2 cells (Left). Survival analysis revealed that the APR-246 treatment prolonged the survival of nude mice (Right).

    Eprenetapopt purchased from MedChemExpress. Usage Cited in: Clin Cancer Res. 2025 Jul 8.  [Abstract]

    IHC staining of intracranial tumors in nude mice demonstrated that Eprenetapopt (APR-246; ip; 400 mg/kg; On the first, third, fifth, and seventh days following the initial imaging session) treatment decreased the protein levels of both UBE2T and Ki-67.

    Eprenetapopt purchased from MedChemExpress. Usage Cited in: Clin Cancer Res. 2025 Jul 8.  [Abstract]

    IF was used to evaluate the effect of Eprenetapopt (APR-246 ) treatment (20 µmol/L, 24 hours) on the distribution and expression of fibrillarin in SG2 and GBM22 cells.

    Eprenetapopt purchased from MedChemExpress. Usage Cited in: Sci Adv. 2022 Sep 16;8(37):eabm9427.  [Abstract]

    Percentage (%) of dead cells [as determined by % PI+ cells] and percentage of cell confluency following treatment for 24 hours with 50 μM Eprenetapopt with or without 50 μM zVAD-FMK (pan-caspase inhibitor), 12.5 μM Fer-1 (lipophilic antioxidant), 6.25 μM CPX (iron chelator), or 2.5 mM NAC (cysteine supplement) in H1299 (left) and FLO-1 cells (right).

    Eprenetapopt purchased from MedChemExpress. Usage Cited in: Sci Adv. 2022 Sep 16;8(37):eabm9427.  [Abstract]

    Eprenetapopt (50 μM 24 h) induced ferroptosis in H1299 and FLO-1 cells.
    • Biological Activity

    • 순도&문서

    • References

    • 고객리뷰

    제품 설명

    Eprenetapopt (APR-246) is a first-in-class, small molecule that restores wild-type p53 functions in TP53-mutant cells. Eprenetapopt triggers apoptosis in tumor cells. Eprenetapopt also targets the selenoprotein thioredoxin reductase 1 (TrxR1), a key regulator of cellular redox balance[1][2][3].

    IC50 & Target

    p53 activator[1]
    TrxR1 inhibitor[1]

    In Vitro

    Eprenetapopt inhibits both recombinant TrxR1 in vitro and TrxR1 in cells. Cellular TrxR1 activity is inhibited by Eprenetapopt irrespective of p53 status. Eprenetapopt can directly affect cellular redox status via targeting of TrxR1. Several small molecules have been shown to restore wild-type activity to mutant p53, including CP-31398, PRIMA-1 and Eprenetapopt, MIRA, STIMA, PhiKan-083 and NSC319726. PRIMA-1 and its methylated analog Eprenetapopt promote correct folding of mutant p53, induce cell death by apoptosis, and inhibit tumor growth in mice. Eprenetapopt has also been shown to reactivate mutant forms of the p63 and p73 proteins that share high structural homology with p53[1].
    Eprenetapopt is a powerful apoptosis-inducing agent. Eprenetapopt can enhance apoptosis in mutant p53 carrying cells, compared to the p53 null parental cells. Most p53 mutants are in complex with Hsp70 proteins. Eprenetapopt treatment increases Hsp70 expression and nucleolar translocation, in parallel with the induction of nucleolar accumulation of mutant p53. Several lines of evidence suggest that Eprenetapopt can also act independently of the p53 status of the cell. It can radiosensitize prostate carcinoma cell lines with mutant or wild type p53 and p53-/- cells as well. Introduction of mutant p53 (p53ser249 or p53gln248) into p53-/- hepatocarcinoma cells increases sensitivity to Eprenetapopt without the induction of p53 target genes.Eprenetapopt regularly induces apoptosis in mutant p53 expressing cells[2].

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

    분자량

    199.25

    화학식

    C10H17NO3

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    O=C1C(COC)(CO)N2CCC1CC2

    선적

    Room temperature in continental US; may vary elsewhere.

    보관
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 2 years
    -20°C 1 year
    용액&용해도
    In Vitro: 

    H2O : 50 mg/mL (250.94 mM; Need ultrasonic)

    DMSO : 50 mg/mL (250.94 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 5.0188 mL 25.0941 mL 50.1882 mL
    5 mM 1.0038 mL 5.0188 mL 10.0376 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.

    * 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.

    • 몰농도 계산기

    • 농도 희석 계산기

    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: ≥ 2.5 mg/mL (12.55 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 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: ≥ 2.5 mg/mL (12.55 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 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 (501.88 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).
    순도&문서

    Purity: 99.52%

    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
    H2O / DMSO 1 mM 5.0188 mL 25.0941 mL 50.1882 mL 125.4705 mL
    5 mM 1.0038 mL 5.0188 mL 10.0376 mL 25.0941 mL
    10 mM 0.5019 mL 2.5094 mL 5.0188 mL 12.5471 mL
    15 mM 0.3346 mL 1.6729 mL 3.3459 mL 8.3647 mL
    20 mM 0.2509 mL 1.2547 mL 2.5094 mL 6.2735 mL
    25 mM 0.2008 mL 1.0038 mL 2.0075 mL 5.0188 mL
    30 mM 0.1673 mL 0.8365 mL 1.6729 mL 4.1824 mL
    40 mM 0.1255 mL 0.6274 mL 1.2547 mL 3.1368 mL
    50 mM 0.1004 mL 0.5019 mL 1.0038 mL 2.5094 mL
    60 mM 0.0836 mL 0.4182 mL 0.8365 mL 2.0912 mL
    80 mM 0.0627 mL 0.3137 mL 0.6274 mL 1.5684 mL
    100 mM 0.0502 mL 0.2509 mL 0.5019 mL 1.2547 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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      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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    상품명:
    Eprenetapopt
    Cat. No.:
    HY-19980
    수량:
    MCE Japan Authorized Agent: