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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC76848 | Methylspinazarin |
Methylspinazarin is a potent inhibitor of catechol O-methyltransferase (COMT, IC50 = 0.8 μg/ml) that can be isolated from Streptomyces. Methylspinazarin is selective for COMT over tyrosine hydroxylase.
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| DC11485 | Tolcapone Featured |
Tolcapone is an orally active catechol-O-methyltransferase (COMT) inhibitor.
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| DC40579 | 5-Hydroxyferulic acid |
5-Hydroxyferulic acid is a hydroxycinnamic acid and is a metabolite of the phenylpropanoid pathway. 5-Hydroxyferulic acid is a precursor in the biosynthesis of sinapic acid and is also a COMT non-esterifed substrate.
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| DC28087 | 3-O-Methyltolcapone |
3-O-Methyltolcapone (Ro 40-7591) 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.
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| DC11094 | Neluxicapone |
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