S82780 |
Entacapone |
源叶(MedMol) | 99% |
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- 产品描述: Entacapone (OR-611) 抑制儿茶酚-O-甲基转移酶(COMT)活性,IC50为151 nM。Entacapone 是一种 FTO demethylation 的抑制剂,IC50为3.5 μM,可用于代谢紊乱的研究
- 靶点: COMT:151 nM;Transferase
- 体外研究:
Entacapone在不同组织中抑制catechol-O-methyltransferase(COMT)的IC50值大体相似,包括肝脏,十二指肠, 肾脏和肺, 但是entacapone在这些组织中抑制效果比tolcapone更好。 Entacapone (< 100 μM)可以有效抑制α-syn和β-amyloid (Aβ) 齐聚反应和原纤维生成同时可以保护PC12细胞免受这两种蛋白聚集诱导的细胞外毒性
- 体内研究:
Entacapone administration reduced body weight and lowered fasting blood glucose concentrations in diet-induced obese mice.
- 细胞实验: Cell lines: PC12 cells Concentrations: 5 μM Incubation Time: 72 h Method: Cells were treated with various concentrations of drug for 72 h.
- 动物实验: Animal Models: Male C57BL/6 mice Dosages: 600 mg/kg Administration: p.o.
- 参考文献:
1. De Santi C, et al. Catechol-O-methyltransferase: variation in enzyme activity and inhibition by entacapone and tolcapone. Eur J Clin Pharmacol, 1998, 54(3), 215-219. 2. Di Giovanni S, et al. Entacapone and tolcapone, two catechol O-methyltransferase inhibitors, block fibril formation of alpha-synuclein and beta-amyloid and protect against amyloid-induced toxicity. J Biol Chem, 2010, 285(20), 14941-14954. 3. Jenner P, et al. Avoidance of dyskinesia: preclinical evidence for continuous dopaminergic stimulation. Neurology, 2004, 62(1 Suppl 1), S47-55. 4. Hamaue N, et al. Entacapone, a catechol-O-methyltransferase inhibitor, improves the motor activity and dopamine content of basal ganglia in a rat model of Parkinson's disease induced by Japanese encephalitis virus. Brain Res, 2010, 1309, 110-115. 5. Peng S, et al. Identification of entacapone as a chemical inhibitor of FTO mediating metabolic regulation through FOXO1. Sci Transl Med. 2019 Apr 17;11(488):eaa
- 溶解性: Soluble in DMSO、Ethanol
- 保存条件: 2-8℃
- 配置溶液浓度参考:
1mg 5mg 10mg 1 mM 3.276 ml 16.378 ml 32.756 ml 5 mM 0.655 ml 3.276 ml 6.551 ml 10 mM 0.328 ml 1.638 ml 3.276 ml 50 mM 0.066 ml 0.328 ml 0.655 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)