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TIPARP-IN-1 (Compound 15) is a selective inhibitor of PARP7 (TIPARP, also known as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) inducible PARP) with an IC50 value of 2.15 nM. By inhibiting TIPARP, TIPARP-IN-1 can restore the IFN signaling pathway in tumors. In the tumor microenvironment, it selectively activates anti-tumor immune responses while avoiding the systemic production of cytokines. TIPARP-IN-1 is applicable for research in head and neck squamous cell carcinoma.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | TIPARP-IN-1 (Compound 15) is a selective inhibitor of PARP7 (TIPARP, also known as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) inducible PARP) with an IC50 value of 2.15 nM. By inhibiting TIPARP, TIPARP-IN-1 can restore the IFN signaling pathway in tumors. In the tumor microenvironment, it selectively activates anti-tumor immune responses while avoiding the systemic production of cytokines. TIPARP-IN-1 is applicable for research in head and neck squamous cell carcinoma. |
| Targets&IC50 | PARP7:2.15 nM |
| Molecular Weight | 503.45 |
| Formula | C22H23F6N5O2 |
| Cas No. | 3106183-96-1 |
| Smiles | C(=O)([C@H]1C[C@@H](CC=2C=C(C(F)(F)F)C(=O)NC2)C1)N3C[C@@H](C)N(CC3)C=4N=CC(C(F)(F)F)=CN4 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
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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