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COMT

COMT (catechol-O-methyltransferase) is one of several enzymes that degrade catecholamines such as dopamine, epinephrine, and norepinephrine.

Products for  COMT

  1. Cat.No. Product Name Information
  2. GC66369 3-O-Methyltolcapone 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. 3-O-Methyltolcapone D7  Chemical Structure
  3. GC62809 5-Hydroxyferulic acid 5-Hydroxyferulic acid is a hydroxycinnamic acid and is a metabolite of the phenylpropanoid pathway. 5-Hydroxyferulic acid  Chemical Structure
  4. GC17334 Entacapone A reversible COMT inhibitor Entacapone  Chemical Structure
  5. GC18091 Entacapone sodium salt COMT inhibitor Entacapone sodium salt  Chemical Structure
  6. GC12535 Flopropione 5-HT receptor antagonist Flopropione  Chemical Structure
  7. GC65175 Nebicapone Nebicapone (BIA 3-202), a reversible catechol-O-methyltransferase (COMT) inhibitor, is mainly metabolized by glucuronidation. Nebicapone  Chemical Structure
  8. GC14223 Nitecapone S-COMT inhibitor Nitecapone  Chemical Structure
  9. GC36811 Opicapone A COMT inhibitor Opicapone  Chemical Structure
  10. GC14843 Serotonin HCl Endogenous 5-HT receptor agonist Serotonin HCl  Chemical Structure
  11. GC17921 Tolcapone A reversible COMT inhibitor Tolcapone  Chemical Structure

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