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PU139 is a novel inhibitor of histone acetyltransferase (HAT).

| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $48 | In Stock | |
| 5 mg | $105 | In Stock | |
| 10 mg | $182 | In Stock | |
| 25 mg | $397 | In Stock | |
| 50 mg | $573 | In Stock | |
| 100 mg | $798 | In Stock | |
| 200 mg | $1,060 | In Stock |
| Description | PU139 is a novel inhibitor of histone acetyltransferase (HAT). |
| Targets&IC50 | CBP:2.49 μM (IC50), p300:5.35 μM (IC50), GCN5:8.39 μM (IC50), PCAF:9.74 μM (IC50) |
| In vitro | PU139 inhibits cell growth with GI50s of <60 μM (A431, A549, A2780, HCT116, HepG2, SW480, U-87 MG and SK-N-SH and MCF7 cells). PU139 (0-100 μM; 24-72 hours) triggers caspase-independent cell death in the neuroblastoma cell line SK-N-SH[1]. |
| In vivo | PU139 (25 mg/kg; i.p.) enhances the growth-inhibitory effects of the chemotherapeutic agent Doxorubicin. |
| Synonyms | PU-139, PU 139 |
| Molecular Weight | 246.26 |
| Formula | C12H7FN2OS |
| Cas No. | 158093-65-3 |
| Smiles | Fc1ccc(cc1)-n1sc2ncccc2c1=O |
| Relative Density. | 1.473 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: 1 mg/mL (4.06 mM), Sonication is recommended. | ||||||||||
Solution Preparation Table | |||||||||||
DMSO
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