Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6708 |
Tolcapone
Tasmar,Ro 40-7592,托卡朋 |
Apoptosis; Beta Amyloid; Transferase | Apoptosis; Metabolism; Neuroscience |
Tolcapone (Ro 40-7592) 是一种选择性,具有口服活性的外周和中枢COMT 抑制剂,在肝脏中对 COMT 的IC50为 773 nM。它还是一种 α-syn 和 Aβ42 寡聚和原纤维形成的有效抑制剂,可诱导氧化应激导致神经母细胞瘤细胞凋亡和抑制肿瘤生长。 | |||
T13181 |
Tolcapone D7
Ro 40-7592 D7 |
Transferase | Metabolism |
Tolcapone D7 is a deuterium-labeled Tolcapone. Tolcapone is a selective and orally active inhibitor of COMT. | |||
T10119 |
3-O-Methyltolcapone
Ro 40-7591 |
Transferase | Metabolism |
3-O-Methyltolcapone (Ro 40-7591) is a metabolite of Tolcapone which is a potent COMT inhibitor. Tolcapone crosses the blood-brain barrier and can be used for treatment of Parkinson's disease. | |||
T10118 |
3-O-Methyltolcapone D7
Ro 40-7591 D7 |
Transferase | Metabolism |
3-O-Methyltolcapone D7 (Ro 40-7591 D7) is a deuterium labeled 3-O-Methyltolcapone. 3-O-Methyltolcapone (Ro 40-7591) is a metabolite of Tolcapone which is a potent COMT inhibitor. Tolcapone crosses the blood-brain barrier and can be used for treatment of P | |||
T28593 |
Ro 61-1448
Ro-61-1448,Ro 611448 |
||
Ro 61-1448 is a metabolite of tolcapone, a catechol-O-methyltransferase inhibitor. | |||
T11207 | Entacapone sodium salt | Others | Others |
Entacapone sodium salt inhibits catechol-O-methyltransferase(COMT) with similar IC50 in different tissues including live, duodenum, kidney and lung, but entacapone is more active than tolcapone in those tissues. Entacapone (< 100 μM) is a potent inhibitor of α-syn and β-amyloid (Aβ) oligomerization and fibrillogenesis, and also protects against extracellular toxicity induced by the aggregation of both proteins in PC12 cells.Entacapone sodium salt is a specific, potent, peripherally acting catech... |