1. Stem Cell/Wnt
  2. Wnt
  3. BML-284

BML-284 is a potent and cell-permeable Wnt signaling activator. BML-284 induces TCF-dependent transcriptional activity with an EC50 of 700 nM.

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

CAS No. : 853220-52-7

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Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
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Customer Review

Based on 41 publication(s) in Google Scholar

Other Forms of BML-284:

Top Publications Citing Use of Products

41 Publications Citing Use of MCE BML-284

WB
Cell Imaging/Staining
RT-PCR
IF
In Vivo Efficacy Study

    BML-284 purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2023 Aug 25;9(1):312.  [Abstract]

    Protein level of β-catenin, PPARγ, and GAPDH for RCT-FAPs (FAPs isolated from supraspinatus muscle one week after tendon tears) with or without β-catenin agonist BML-284 (1 μM) treatment.

    BML-284 purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2023 Aug 25;9(1):312.  [Abstract]

    The oil red staining and statistical analysis of RCT-FAPs after 7-day adipogenic induction in AIM with DMSO or BML-284 (1 μM).

    BML-284 purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2023 Aug 25;9(1):312.  [Abstract]

    Relative mRNA expression level of adipogenic genes for RCT-FAPs after 7-day adipogenic induction in AIM with DMSO or BML-284 (1 μM).

    BML-284 purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2023 Aug 25;9(1):312.  [Abstract]

    Immunofluorescence staining of perilipin1 for supraspinatus muscles from the DMSO group and BML-284 (1 μM) group.

    BML-284 purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2023 Aug 25;9(1):312.  [Abstract]

    Gross appearance of supraspinatus muscles from the DMSO and BML-284 (1 μM) treatment groups.

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    • Customer Review

    Description

    BML-284 is a potent and cell-permeable Wnt signaling activator. BML-284 induces TCF-dependent transcriptional activity with an EC50 of 700 nM[1].

    IC50 & Target

    EC50: 700 nM (TCF-dependent transcriptional activity)[1]

    Cellular Effect
    Cell Line Type Value Description References
    HCT-116 IC50
    0.52 μM
    Compound: BML284
    Antiproliferative activity against human HCT-116 cells assessed as reduction in cell viability measured after 72 hrs
    Antiproliferative activity against human HCT-116 cells assessed as reduction in cell viability measured after 72 hrs
    [PMID: 38430854]
    HeLa IC50
    0.09 μM
    Compound: BML284
    Antiproliferative activity against human HeLa cells assessed as reduction in cell viability measured after 72 hrs
    Antiproliferative activity against human HeLa cells assessed as reduction in cell viability measured after 72 hrs
    [PMID: 38430854]
    K562 IC50
    0.1 μM
    Compound: BML284
    Antiproliferative activity against human K562 cells assessed as reduction in cell viability measured after 72 hrs
    Antiproliferative activity against human K562 cells assessed as reduction in cell viability measured after 72 hrs
    [PMID: 38430854]
    MCF7 IC50
    0.69 μM
    Compound: BML284
    Antiproliferative activity against human MCF7 cells assessed as reduction in cell viability measured after 72 hrs
    Antiproliferative activity against human MCF7 cells assessed as reduction in cell viability measured after 72 hrs
    [PMID: 38430854]
    MOLM-13 IC50
    0.19 μM
    Compound: BML284
    Antiproliferative activity against human MOLM-13 cells assessed as reduction in cell viability measured after 72 hrs
    Antiproliferative activity against human MOLM-13 cells assessed as reduction in cell viability measured after 72 hrs
    [PMID: 38430854]
    In Vitro

    BML-284 (10 μM; 24 hours) significantly increases the migration and invasion of both MNK45 and AGS cells and partially restores the migratory and invasive abilities of cells inhibited by pizotifen (HY-B0115)[1].
    BML-284 (10 μM; 24 hours) induces the expression of β-catenin significantly when compared with the NC group. It also partially reverses the effects induced by pizotifen on E-cadherin and N-cadherin expression in MNK45 and AGS cells compared with the pizotifen-treated group[1].

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

    Western Blot Analysis[2]

    Cell Line: Human gastric cancer cell lines MNK45 and AGS[1]
    Concentration: 10 µM
    Incubation Time: 24 hours
    Result: Induced β-catenin expression and reserved E-cadherin and N-cadherin expression in MNK45 and AGS cells.
    In Vivo

    BML-284 (10 ng) combines with Pyrimethanil (4 mg/L) could partially rescue the malformed phenotype and cardiac defects induced by Pyrimethanil in Tg (myl7:EGFP) transgenic embryos at 5.5 hpf are transferred into plates with 20 embryos[1].

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

    Molecular Weight

    350.37

    Formula

    C19H18N4O3

    CAS No.
    Appearance

    Solid

    Color

    White to yellow

    SMILES

    NC1=NC(C2=CC=CC(OC)=C2)=CC(NCC3=CC=C(OCO4)C4=C3)=N1

    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 : ≥ 100 mg/mL (285.41 mM; 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 2.8541 mL 14.2706 mL 28.5413 mL
    5 mM 0.5708 mL 2.8541 mL 5.7083 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:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.08 mg/mL (5.94 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.
    • Protocol 2

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

      Solubility: ≥ 2.08 mg/mL (5.94 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 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.
    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

    Dosage

    mg/kg

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    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: 99.99%

    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, 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 2.8541 mL 14.2706 mL 28.5413 mL 71.3531 mL
    5 mM 0.5708 mL 2.8541 mL 5.7083 mL 14.2706 mL
    10 mM 0.2854 mL 1.4271 mL 2.8541 mL 7.1353 mL
    15 mM 0.1903 mL 0.9514 mL 1.9028 mL 4.7569 mL
    20 mM 0.1427 mL 0.7135 mL 1.4271 mL 3.5677 mL
    25 mM 0.1142 mL 0.5708 mL 1.1417 mL 2.8541 mL
    30 mM 0.0951 mL 0.4757 mL 0.9514 mL 2.3784 mL
    40 mM 0.0714 mL 0.3568 mL 0.7135 mL 1.7838 mL
    50 mM 0.0571 mL 0.2854 mL 0.5708 mL 1.4271 mL
    60 mM 0.0476 mL 0.2378 mL 0.4757 mL 1.1892 mL
    80 mM 0.0357 mL 0.1784 mL 0.3568 mL 0.8919 mL
    100 mM 0.0285 mL 0.1427 mL 0.2854 mL 0.7135 mL
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    Help & FAQs
    • 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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    Product Name:
    BML-284
    Cat. No.:
    HY-19987
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