Tolcapone
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Tolcapone
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Systematic (IUPAC) name | |
2-dihydroxyamino-4- (4-methylbenzoyl)- cyclohexa-2,4-diene-1,6-dione | |
Identifiers | |
CAS number | |
ATC code | N04 |
PubChem | |
DrugBank | |
Chemical data | |
Formula | C14H11NO5 |
Mol. mass | 273.241 g/mol |
Pharmacokinetic data | |
Bioavailability | 65% |
Protein binding | >99.9% |
Metabolism | ? |
Half life | 2-3.5 hours |
Excretion | ? |
Therapeutic considerations | |
Pregnancy cat. |
C(US) |
Legal status | |
Routes | Oral |
Tolcapone is a drug that inhibits the enzyme catechol-O-methyl transferase (COMT). It is used in the treatment of Parkinson's disease as an adjunct to levodopa/carbidopa medication. It is a yellow, odorless, non-hygroscopic, crystalline compound with a relative molecular mass of 273.25. The chemical name of tolcapone is 3,4-dihydroxy-4’-methyl-5-nitrobenzophenone. Its empirical formula is C14H11NO5.
Tolcapone has the ability to cross the blood-brain barrier and thus exerts its COMT inhibitory effects in the CNS as well as in the periphery.
Tolcapone has demonstrated significant hepatotoxicity that limits the drugs therapeutic utility to a drug of last resort. Entacapone, another COMT inhibitor, is a more popular selection for L-Dopa adjunct therapy in the treatment of Parkinson's Disease because it has a better side effect and toxicity profile.