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Entacapone, MedChemExpress
Description
Entacapone inhibits COMT from rat brain, erythrocytes and liver with IC50 values of 10 nM, 20 nM, and 160 nM, respectively. Entacapone is selective for COMT over other catecholamine metabolizing enzymes, including MAO-A, MAO-B, phenolsulphotransferase M (PST-M) and PST-P (IC50s>50 μM). Entacapone can be used for the research of Parkinson's disease. Entacapone serves as a inhibitor of FTO demethylation with an IC50 of 3.5 μM, can be used for the research of metabolic disorders.
Specifications
Specifications
| Chemical Name or Material | Entacapone |
| CAS | 130929-57-6 |
| Color | Yellow |
| Purity Grade Notes | Research |
| Molecular Formula | C14H15N3O5 |
| Quantity | 10 mg |
| Solubility Information | DMSO : 33.33 mg/mL (109.17 mM; Need ultrasonic) ∣H2O : 2 mg/mL (6.55 mM; ultrasonic and adjust pH to 10 with NaOH) |
| SMILES | O=C(N(CC)CC)/C(C#N)=C/C1=CC([N+]([O-])=O)=C(O)C(O)=C1 |
| Molecular Weight (g/mol) | 305.29 |
| Formula Weight | 305.29 |
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Research purposes only
Product Title
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