Compound inhibiting activation of the enzyme Erk 1/2 to be used in the treatment of neurodegenerative illnesses
The present invention relates to a compound of formula (I) for use as a medicine, in particular for use in the treatment of diseases mediated by the actvation of the protein kinase Erk1/2, such as neurogenerative illnesses like Alzheimer's and related dementia, epilepsy, Parkinson's disease, Huntington's disease, or stroke, and likewise relates to the pharmaceutical compositions containing said compound. The compound of formula (I) effectively inhibits the activation of the enzyme Erk1/2 induced by the tissue plasminogen activator (TPA) and also effectively inhibits the apoptosis generated by the β-amyloid peptide.
1. A compound having the formula
or a pharmaceutically acceptable salt thereof.
2. A method for the treatment of a disease mediated by the activation of the protein kinase Erk 1/2 in a patient comprising administering the compound of claim 1 .
3. The method of claim 2 wherein the disease mediated by the activation of the protein kinase Erk 1/2 is a neurodegenerative illness.
4. The method of claim 3 , wherein the disease is selected from the group formed by Alzheimer's disease and related dementias, epilepsy, Parkinson's disease, Huntington's disease or stroke.
5. The method of claim 4 , wherein the disease is selected from the group formed by Alzheimer's disease and related dementias, and epilepsy.
6. The method of to claim 5 , wherein the disease is Alzheimer's disease and related dementias.
7. The method of claim 5 , wherein the disease is epilepsy.
8. The method of claim 2 wherein said compound comprises an additional therapeutic agent.
9. A pharmaceutical composition characterised in that it comprises a therapeutically effective quantity of the compound of claim 1 or a pharmaceutically acceptable salt thereof, and at least one pharmaceutical excipient.
10. The pharmaceutical composition according to claim 9 , further comprising an additional therapeutic agent.
11. The method of claim 2 wherein the compound is administered by oral route, by parenteral route, by means of a spray for inhalation, by rectal route, by nasal route, or by means of an implanted reservoir.