| MDL | - |
|---|---|
| Molecular Weight | 284.27 |
| Molecular Formula | C15H12N2O4 |
| SMILES | O=C(N1O)N(C2=CC=C(OC)C=C2)C3=C(C=CC=C3)C1=O |
FEN1 inhibition selectively impairs proliferation of colon cancer cells deficient in Cdc4 and Mre11a , both frequently mutated in colorectal cancers. FEN1 has also emerged as a potential chemosensitizing target due to its role in LP-BER since it is critical for repair of Methyl methanesulfonate-induced alkylation damage, and its knockdown or inhibition increases sensitivity to Temozolomide in glioblastoma and colorectal cancer cell lines [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
| Powder | -20°C | 3 years |
|---|---|---|
| 4°C | 2 years | |
| In solvent | -80°C | 6 months |
| -20°C | 1 month |
DMSO : 250 mg/mL ( 879.45 mM ; Need ultrasonic)
| Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
|---|
| 1 mM | 3.5178 mL | 17.5889 mL | 35.1778 mL |
| 5 mM | 0.7036 mL | 3.5178 mL | 7.0356 mL |
| 10 mM | 0.3518 mL | 1.7589 mL | 3.5178 mL |