COMT
COMT (catechol-O-methyltransferase) is one of several enzymes that degrade catecholamines such as dopamine, epinephrine, and norepinephrine.
Products for COMT
- Cat.No. Product Name Information
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GC66369
3-O-Methyltolcapone D7
Ro 40-7591 D7
3-O-Methyltolcapone D7 (Ro 40-7591 D7) is a deuterium labeled 3-O-Methyltolcapone. 3-O-Methyltolcapone is a metabolite of Tolcapone. Tolcapone is an orally active, reversible, selective and potent COMT inhibitor. Tolcapone crosses the blood-brain barrier, and can be used for treatment of Parkinson's disease. -
GC62809
5-Hydroxyferulic acid
5-Hydroxyferulic acid is a hydroxycinnamic acid and is a metabolite of the phenylpropanoid pathway.
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GC17334
Entacapone
OR-611
Entacapone is a potent, reversible, peripherally acting and orally active inhibitor of catechol-O-methyltransferase (COMT), which effectively inhibits rat liver total COMT with IC50 and Ki values of 20.1nM and 10.7nM, respectively. -
GC18091
Entacapone sodium salt
COMT inhibitor
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GC12535
Flopropione
5-HT receptor antagonist
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GC71152
hMAO-B/MB-COMT-IN-1
hMAO-B/MB-COMT-IN-1 is a dual MAO-B/MB-COMT inhibitor (IC50s: 2.5 μΜ for hMAO-B, 3.84 μΜ for MB-COMT).
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GC65175
Nebicapone
BIA 3-202
Nebicapone (BIA 3-202), a reversible catechol-O-methyltransferase (COMT) inhibitor, is mainly metabolized by glucuronidation. -
GC14223
Nitecapone
OR-462
S-COMT inhibitor -
GC36811
Opicapone
BIA 9-1067
A COMT inhibitor -
GC14843
Serotonin HCl
5-HT, 5-Hydroxytryptamine
Serotonin HCl a neurotransmitter, is a key messenger that mediates several central and peripheral functions in the human body.
-
GC17921
Tolcapone
Ro 40-7592
A reversible COMT inhibitor