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MYF-03-69 (TEAD-IN-3) is a covalent and irreversible pan-TEAD inhibitor with IC₅₀ values of 385/143/558/173 nM for TEAD1/TEAD2/TEAD3/TEAD4, respectively. MYF-03-69 inhibits TEAD transcriptional activity (IC₅₀ = 56 nM), upregulates the pro-apoptotic gene BMF, and suppresses mesothelioma cancer cells with defective Hippo signaling, making it suitable for malignant pleural mesothelioma (MPM).

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $893 | 6-8 weeks | 6-8 weeks | |
| 50 mg | $1,160 | 6-8 weeks | 6-8 weeks | |
| 100 mg | $1,860 | 6-8 weeks | 6-8 weeks |
| Description | MYF-03-69 (TEAD-IN-3) is a covalent and irreversible pan-TEAD inhibitor with IC₅₀ values of 385/143/558/173 nM for TEAD1/TEAD2/TEAD3/TEAD4, respectively. MYF-03-69 inhibits TEAD transcriptional activity (IC₅₀ = 56 nM), upregulates the pro-apoptotic gene BMF, and suppresses mesothelioma cancer cells with defective Hippo signaling, making it suitable for malignant pleural mesothelioma (MPM). |
| Targets&IC50 | TEAD4:173 nM, TEAD1:385 nM, TEAD2:143 nM, TEAD3:558 nM |
| In vitro | MYF-03-69 (0–10 μM; 5 days) selectively inhibits proliferation of mesothelioma cells with defective Hippo signaling (e.g., NCI-H226, MSTO-211H) with impaired Hippo signaling, while exhibiting minimal cytotoxicity toward normal mesothelial cells or cancer cells with intact Hippo signaling [1]. MYF-03-69 (0.1–10 μM; 48 h) induced G1 phase cell cycle arrest in NCI-H226 and MSTO-211H cells [1]. MYF-03-69 (2 μM) inhibits TEAD protein palmitoylation, downregulates YAP-TEAD target genes (e.g., CTGF, CYR61, ANKRD1) in NCI-H226 cells, and upregulates the pro-apoptotic gene BMF [1]. |
| Synonyms | TEAD-IN-3, MYF03-69, MYF 03-69 |
| Molecular Weight | 443.42 |
| Formula | C22H20F3N5O2 |
| Cas No. | 2416418-11-4 |
| Smiles | O(CC1=CC=C(C(F)(F)F)C=C1)[C@H]2[C@@H](CN(C(C=C)=O)C2)N3C=C(N=N3)C=4C=CC=NC4 |
| Storage | keep away from moisture,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (180.42 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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