PARP1/2-IN-3 is a potent inhibitor of PARP1 and PARP2, exhibiting IC50 values of 0.2235 nM and <0.001 nM, respectively. This compound effectively inhibits the proliferation of Capan-1 wildtype and AZD2281 or BMN673-resistant cells, with IC50 values ranging from 1.82 to 9.98 nM. Additionally, PARP1/2-IN-3 demonstrates significant antitumor efficacy in murine models, making it a valuable tool for cancer research and therapeutic development targeting PARP pathways.
Fig. 1 · Structure
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PARP1/2-IN-3
PARP1/2 Inhibitor
PARP1/2-IN-3 is a potent inhibitor of PARP1 and PARP2, exhibiting IC50 values of 0.2235 nM and <0.001 nM, respectively. This compound effectively inhibits the proliferation of Capan-1 wildtype and AZD2281 or BMN673-resistant cells, with IC50 values ranging from 1.82 to 9.98 nM. Additionally, PARP1/2-IN-3 demonstrates significant antitumor efficacy in murine models, making it a valuable tool for cancer research and therapeutic development targeting PARP pathways.
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Biological Activity
Specifications
| Manufacturer | Adooq Bioscience |
|---|---|
| Actions | Inhibitor |
| CAS Number | 3032451-58-1 |
| Applications | PARP1/2 Inhibitor |
| Formula | C26H21FN6O3 |
| Molecular Weight | 484.48 |
| SMILES | CC1=CC=C(O1)C2=NN=C3CN(CCN32)C(C4=CC(CC5=NNC(C6=C5C=CC=C6)=O)=CC=C4F)=O |
Storage & Solubility
In Vitro Solubility
Reported Solubility
No reported solubility data are available for this product.
Preparing Stock Solutions
| Concentration | |
|---|---|
Values use four significant digits. Prepare to the final solution volume; this is not the volume of solvent to add.
Stock preparation is unavailable for this product molecular weight.
Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.
Storage
Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.