同义名 : | Entacapone Sodium | |
CAS号 : | 1047659-02-8 | |
货号 : | A891824 | |
分子式 : | C14H14N3NaO5 | |
纯度 : | 98% | |
分子量 : | 327.268 | |
MDL号 : | MFCD28346924 | |
存储条件: |
粉末 Inert atmosphere,2-8°C 液体 -20°C:3-6个月-80°C:12个月 |
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溶解度 : | - | |
动物实验配方: |
生物活性 | |||
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描述 | Entacapone sodium salt is an effective, reversible, peripherally active, and orally administered catechol-O-methyltransferase (COMT) inhibitor. It inhibits COMT in rat brain, erythrocytes, and liver with IC50 values of 10 nM, 20 nM, and 160 nM, respectively. Entacapone sodium salt selectively inhibits COMT over other catecholamine metabolizing enzymes such as MAO-A, MAO-B, phenolsulphotransferase M (PST-M), and PST-P, all with IC50 values greater than 50 µM, and is used in Parkinson's disease research[1]. Entacapone sodium salt acts as an inhibitor of FTO demethylation with an IC50 of 3.5 μM and is utilized in metabolic disorder studies[2]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.06mL 0.61mL 0.31mL |
15.28mL 3.06mL 1.53mL |
30.56mL 6.11mL 3.06mL |
参考文献 |
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