2. Stem Cell/Wnt
  3. Wnt
  4. iCRT 14

iCRT 14 is a novel potent inhibitor of β-catenin-responsive transcription (CRT), with IC50 of 40.3 nM against Wnt responsive STF16 luciferase.

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CAS No. : 677331-12-3

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

Based on 19 publication(s) in Google Scholar

iCRT 14 Related Antibodies

Top Publications Citing Use of Products

    iCRT 14 purchased from MedChemExpress. Usage Cited in: Mater Today Bio. 2024 Jun 1:26:101111.

    The COOME was treated with or without Wnt inhibitor ICRT 14 (1, 3 or 5 μM) for 24 h. Then the treated COOME was co-culture with iMSCs for 3 days. Osteogenic differentiation was evaluated using AP staining.

    iCRT 14 purchased from MedChemExpress. Usage Cited in: Int J Mol Sci. 2023 Dec 22;25(1):217.

    H1650 were pre-treated for 1 h with either 100 nM iCRT14 or 1 nM LGK-974 and were infected with Vpp overnight in the presence of the inhibitors.

    iCRT 14 purchased from MedChemExpress. Usage Cited in: Int J Mol Sci. 2023 Dec 22;25(1):217.

    HEK293T cells were pre-treated for 1 h with either 10 nM iCRT14 or 0.01 nM LGK-974 and were infected with Vpp overnight in the presence of the inhibitors.

    iCRT 14 purchased from MedChemExpress. Usage Cited in: Int J Mol Sci. 2023 Dec 22;25(1):217.

    Effect of disruption of β-catenin pathway on ACE2 RNA levels. H1650 cells were treated with the indicated concentrations of iCRT14 for 24 h and were subsequently harvested for qRT-PCR. The levels of ACE2 RNA were normalized by GAPDH RNA.

    iCRT 14 purchased from MedChemExpress. Usage Cited in: Neurotherapeutics. 2021 Jan;18(1):601-614.  [Abstract]

    On day 16, 18 rats were divided into three groups that received an injection of vehicle, 10 or 30 mg/kg of iCRT14 (ip, single dose). The 30 mg/kg of iCRT14 significantly increased the mechanical threshold for 3 h compared with that in the vehicle group (n = 6, p < 0.05).

    iCRT 14 purchased from MedChemExpress. Usage Cited in: Vet Microbiol. 2020 Sep;248:108804.  [Abstract]

    MDBK cells in 60 mm dishes are pretreated with iCRT14 (10 μM) for 2 hours, after which they are mock infected or infected with BoHV-1 at an MOI of 0.1 in the presence of iCRT14 (10 μM) or DMSO control. After infection for 24 h, the cell lysates are prepared for Western blotting to detect the expression of JNK.

    iCRT 14 purchased from MedChemExpress. Usage Cited in: Cell Death Dis. 2018 Apr 1;9(4):433.  [Abstract]

    rECA109 and rKyse150 cells show preferential activation of DNA damage checkpoint responses upon exposure to ionizing radiation (IR) relative to parental cells. And WNT1 promoted preferential activation of DNA damage response while iCRT14 hinders it.

    View All Wnt Isoform Specific Products:

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    Wnt1 Wnt3 Wnt5 Wnt7 Wnt11

    • Biological Activity

    • Protocol

    • 순도&문서

    • References

    • 고객리뷰

    제품 설명

    iCRT 14 is a novel potent inhibitor of β-catenin-responsive transcription (CRT), with IC50 of 40.3 nM against Wnt responsive STF16 luciferase.

    IC50 & Target

    IC50: 40.3 nM (Wnt responsive STF16 luciferase)[1]
    In Vitro

    iCRT 14 can interfere with TCF binding to DNA in addition to its ability to influence TCF-β-cat interaction[1]. iCRT 14 (10, 25, 50 μM) effectively inhibits cell proliferation in BT-549 cells in a dose- and time-dependent manner, but still less potent than iCRT 3[2].

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

    iCRT 14 Related Antibodies
    In Vivo

    iCRT 14 (50 mg/kg, i.p.) markedly decreases CycD1, proliferation of the tumors in HCT116 xenografts[1].

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

    375.44

    화학식

    C21H17N3O2S
    CAS No.
    Appearance

    Solid

    Color

    Light yellow to yellow

    SMILES

    O=C(S/1)N(C2=CC=CC=C2)C(C1=C\C3=C(C)N(C(C)=C3)C4=CN=CC=C4)=O
    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: 

    DMSO : ≥ 29 mg/mL (77.24 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 2.6635 mL 13.3177 mL 26.6354 mL
    5 mM 0.5327 mL 2.6635 mL 5.3271 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.

    • 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 (6.66 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.
    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.
    순도&문서

    Purity: 99.72%

    SDS (643 KB)

    COA (253 KB) HNMR (175 KB) LCMS (94 KB)

    Handling Instructions (2659 KB)
    References
    Cell Assay 
    [2]

    Cells are seeded at 20,000 cells/well into 96-well plates. After overnight incubation, cells are treated with DMSO or each Wnt inhibitor (iCRT-3, 75 μM; iCRT-5, 200 μM; iCRT-14, 50 μM; IWP-4, 5 μM and XAV-939, 10 μM) for 48 hours. Cell viability is determined using the Cell Titer-Glo luminescent cell viability assay kit. Luminescence is measured using FLUOstar microplate reader. All treatments are performed in triplicate, and each experiment is repeated three times.

    MCE 는 독립적으로 이러한 방법들의 정확성을 확인하지 않았습니다. 참고용으로만 봐주십시오.
    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 2.6635 mL 13.3177 mL 26.6354 mL 66.5885 mL
    5 mM 0.5327 mL 2.6635 mL 5.3271 mL 13.3177 mL
    10 mM 0.2664 mL 1.3318 mL 2.6635 mL 6.6589 mL
    15 mM 0.1776 mL 0.8878 mL 1.7757 mL 4.4392 mL
    20 mM 0.1332 mL 0.6659 mL 1.3318 mL 3.3294 mL
    25 mM 0.1065 mL 0.5327 mL 1.0654 mL 2.6635 mL
    30 mM 0.0888 mL 0.4439 mL 0.8878 mL 2.2196 mL
    40 mM 0.0666 mL 0.3329 mL 0.6659 mL 1.6647 mL
    50 mM 0.0533 mL 0.2664 mL 0.5327 mL 1.3318 mL
    60 mM 0.0444 mL 0.2220 mL 0.4439 mL 1.1098 mL
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    iCRT 14 Related Classifications

    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.

    Keywords:

    iCRT 14677331-12-3iCRT14iCRT-14WntInhibitorinhibitorinhibit

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    상품명:
    iCRT 14
    Cat. No.:
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    SAFETY DATA SHEET (SDS)

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