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VT104 is a potent and orally active YAP/TAZ inhibitor for cancer research. VT104 blocks palmitoylation of endogenous TEAD1 and TEAD3 proteins.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $72 | In Stock | In Stock | |
| 5 mg | $158 | In Stock | In Stock | |
| 10 mg | $248 | In Stock | In Stock | |
| 25 mg | $397 | In Stock | In Stock | |
| 50 mg | $569 | In Stock | In Stock | |
| 100 mg | $786 | - | In Stock | |
| 200 mg | $1,090 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $176 | In Stock | In Stock |
| Description | VT104 is a potent and orally active YAP/TAZ inhibitor for cancer research. VT104 blocks palmitoylation of endogenous TEAD1 and TEAD3 proteins. |
| In vitro | METHODS: Huh7 cells were treated with the pan-TEAD inhibitor VT104 (0.1, 0.5, 1, 2.5, 5 μM) for 72 h and then subjected to WST assay to assess cell number or 24 h for qPCR of ANKRD1, ANLN, and KIF23. RESULTS VT104 reduced Huh7 cell proliferation and inhibited the TAZ-TEAD pathway, with reduced expression of TAZ-TEAD targets ANLN, KIF23, ANKRD1, CTGF, and CD274 in Huh7 cells. [3] |
| In vivo | METHODS: Mice after MET+CTNNB1-S45Y HTVI were treated with VT104 (10 mg/kg/day) for 6 weeks. RESULTS VT104 strongly inhibited HCC development in vivo driven by MET+CTNNB1-S45Y; VT104 significantly reduced Ki67+ proliferation and γH2AX-positive hepatocytes. [3] |
| Molecular Weight | 420.43 |
| Formula | C25H19F3N2O |
| Cas No. | 2417718-25-1 |
| Smiles | C[C@H](NC(=O)c1ccc2c(cccc2c1)-c1ccc(cc1)C(F)(F)F)c1ccccn1 |
| Color | White |
| Appearance | Solid |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 30 mg/mL (71.36 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
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DMSO
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