17
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T75389 | Catechol O-methyltransferase | ||
Catechol O-methyltransferase (COMT) is a magnesium-dependent enzyme that mediates the transfer of methyl groups from S-adenosyl methionine to the hydroxyl group on dopamine, thus converting it to 3-methoxytyramine. COMT ... | |||
T24030 | Entacapone acid | AG1290,AG 1290,AG-1290 | Transferase |
Entacapone acid (AG 1290) is a selective and reversible inhibitor of catechol-O-methyltransferase(COMT). | |||
T16398 | Opicapone | BIA 9-1067 | Transferase |
Opicapone (BIA 9-1067) reduces the ATP content of the cells (IC50: 98 μM). Opicapone is an effective third-generation catechol-O-methyltransferase inhibitor for the research of Parkinson's disease and motor fluctuations. | |||
T2216 | Entacapone | OR-611 | Transferase |
Entacapone (OR-611) is a selective and reversible inhibitor of catechol-O-methyltransferase (COMT). | |||
T6708 | Tolcapone | Tasmar,Ro 40-7592 | Apoptosis , Beta Amyloid , Transferase |
Tolcapone (Ro 40-7592) is a catechol-O-methyltransferase inhibitor used in the therapy of Parkinson disease as adjunctive therapy in combination with levodopa and carbidopa. | |||
T27162 | DHMPA | ||
DHMPA is an inhibitor of catechol-O-methyltransferase (COMT), it also reduces tissue norepinephrine and blood pressure. | |||
T29029 | U-0521 | ||
U-0521, an inhibitor of catechol-O-methyltransferase (COMT), enhances the availability and utilization of levodopa in the brain. | |||
T26797 | BIA 3-335 | BIA-3-335,BIA3335 | |
BIA 3-335, an inhibition of catechol-O-methyltransferase, could have applications for Parkinson's Disease. | |||
T28593 | Ro 61-1448 | Ro-61-1448,Ro 611448 | |
Ro 61-1448 is a metabolite of tolcapone, a catechol-O-methyltransferase inhibitor. | |||
T36122 | 3-O-methyl-L-DOPA (hydrate) | ||
3-O-methyl-L-DOPA is a metabolite of L-DOPA , produced by the activity of catechol O-methyltransferase. 3-O-methyl-L-DOPA may have effects of its own or it may compete with the actions of L-DOPA. | |||
T16279 | Nebicapone | BIA 3-202 | Others |
Nebicapone is a reversible catechol-O-methyltransferase (COMT) inhibitor and is mainly metabolized by glucuronidation. Nebicapone is mainly peripherally acting inhibitor that decreases the biotransformation of L-DOPA to ... | |||
T11207 | Entacapone sodium salt | 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. Entacapo... | |||
T70608 | Cis-Entacapone | ||
cis-Entacapone is a metabolite of the catechol-O-methyltransferase (COMT) inhibitor entacapone. It is also a potential impurity found in commercial preparations of entacapone and a degradant of entacapone formed by UV li... | |||
T26997 | CGP-28014 | ||
CGP-28014 is an inhibitor of catechol-O-methyltransferase. CGP-28014 increases the renal excretion of both dopamine and dihydroxyphenylacetic acid (DOPAC) but does not affect renal sodium handling indicating a different ... | |||
T2209 | Serotonin hydrochloride | 5-HT hydrochloride,5-HT HCl,Serotonin HCl,5-Hydroxytryptamine hydrochloride | 5-HT Receptor , Endogenous Metabolite , Transferase |
Serotonin hydrochloride (Serotonin HCl) is an endogenous 5-HT receptor agonist, a monoamine neurotransmitter in the CNS, and a catechol O-methyltransferase (COMT) inhibitor(Ki=44 μM). | |||
T36207 | Methylspinazarin | ||
Methylspinazarin is a naphthoquinone bacterial metabolite that has been found in Streptomyces and is an inhibitor of catechol O-methyltransferase (COMT; IC50 = 0.8 μg/ml).1 It is selective for COMT over tyrosine hydroxyl... | |||
TMIH-0576 | Tolcapone-d7 | ||
Tolcapone-d7 is a deuterated compound of Tolcapone. Tolcapone has a CAS number of 134308-13-7. Tolcapone is a catechol-O-methyltransferase inhibitor used in the therapy of Parkinson disease as adjunctive therapy in combi... |