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IK-930 is an orally active TEAD inhibitor (EC50 < 0.1 µM) with potent potency.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | $51 | In Stock | In Stock | |
| 10 mg | $84 | In Stock | In Stock | |
| 25 mg | $172 | In Stock | In Stock | |
| 50 mg | $278 | In Stock | In Stock | |
| 100 mg | $452 | - | In Stock |
| Description | IK-930 is an orally active TEAD inhibitor (EC50 < 0.1 µM) with potent potency. |
| Targets&IC50 | TEAD:<0.1 µM(EC50) |
| In vitro | IK-930 (0-1 μM) is a potent and selective TEAD inhibitor.[2] |
| In vivo | IK-930 (compound I-32) (10 mg/kg; p.o.) demonstrates favorable pharmacokinetic parameters in BALB/c mice, with a Cmax of 1088 ng/mL and an AUC 0-last of 4581 ng·h/mL.[1] |
| Synonyms | compound I-32 |
| Molecular Weight | 424.44 |
| Formula | C19H19F3N4O2S |
| Cas No. | 2563892-44-2 |
| Smiles | N(CC1=CC=C(C(F)(F)F)C=C1)C2=C(C=C(S(NC)(=O)=O)C=C2)C=3N=CN(C)C3 |
| Relative Density. | 1.36 g/cm3 (Predicted) |
| 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: 90.0 mg/mL (212.0 mM), Sonication and heating to 60℃ are recommended. | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (7.77 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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