Centrally-active ghrelin agonist and medical uses thereof
The new compound 3-(1-(2,3-dichloro-4-methoxyphenyl) ethyl)-1-methyl-1-(1,3, 3-trimethylpiperidin-4-yl)urea monohydrochloride salt has a high capability to permeate through the blood-brain barrier and to display, at central nervous system level, a consistent ghrelin agonist activity; the compound is effective in the treatment and/or prevention of a medical condition mediated by the ghrelin receptor in the central nervous system. In particular, in experimental tests, the compound has shown high efficacy in the treatment of neurotoxic damage, with a useful combined pattern of neuroprotective effects both at central and peripheral level. The compound is further useful in the treatment of conditions which require a reduction of the heart rate. The compound is pharmacologically active at low to moderate doses, thus showing a favourable therapeutic index.
1. A method of treating a medical condition mediated by the ghrelin receptor in the central nervous system of a subject in need thereof, the method comprising administering compound 3-(1-(2,3-dichloro-4-methoxyphenyl)ethyl)-1-methyl-1-(1,3,3-trimethylpiperidin-4-yl)urea monohydrochloride salt to the subject.
2. The method of claim 1 , wherein said medical condition is neurodegeneration, neuropathy, neuropathic pain, encephalomyelitis, Parkinson's Disease, Alzheimer's Disease, cognitive disorders, vagal hyperstimulation, or tachycardia.
3. The method of claim 2 , wherein said neuropathy is a chemotherapy-induced neuropathy.
4. The method of claim 3 , wherein said chemotherapy-induced neuropathy is induced by a proteasome inhibitor or an alkylating agent.
5. The method of claim 4 , wherein said proteasome inhibitor is bortezomib, carfilzomib, ixazomib, oprozomib, delanzomib, marizomib, MG-132, ONX-0914, VR-23, celastrol, or epoxomicin.
6. The method of claim 4 , wherein said alkylating agent is cisplatin or carboplatin.
7. The method of claim 2 , wherein said tachycardia is a chemotherapy-induced tachycardia.
8. The method of claim 1 , wherein said compound is administered in a dose amount ranging from about 0.03 and to about 10 mg, expressed as free base.
9. The method of claim 1 , wherein said compound is administered externally to the central nervous system.
10. The method of claim 9 , wherein said compound is administered by an oral, peroral, buccal, sublingual, ocular, percutaneous, transcutaneous, intravenous, intramuscular, inhalatory or rectal route.
11. The method of claim 3 , wherein said compound is administered in a dose amount ranging from about 0.03 to about 10 mg, expressed as free base.
12. The method of claim 4 , wherein said compound is administered in a dose amount ranging from about 0.03 to about 10 mg, expressed as free base.
13. The method of claim 7 , wherein said compound is administered in a dose amount ranging from about 0.03 to about 10 mg, expressed as free base.
14. The method of claim 3 , wherein said compound is administered externally to the central nervous system.
15. The method of claim 4 , wherein said compound is administered externally to the central nervous system.
16. The method of claim 7 , wherein said compound is administered externally to the central nervous system.
17. A method of preventing a medical condition mediated by the ghrelin receptor in the central nervous system of a subject in need thereof, the method comprising administering compound 3-(1-(2,3-dichloro-4-methoxyphenyl)ethyl)-1-methyl-1-(1,3,3-trimethylpiperidin-4-yl)urea monohydrochloride salt to the subject, wherein the medical condition is chemotherapy-induced neuropathy.
18. The method of claim 17 , wherein said chemotherapy-induced neuropathy is induced by a proteasome inhibitor or an alkylating agent.
19. The method of claim 18 , wherein said proteasome inhibitor is bortezomib, carfilzomib, ixazomib, oprozomib, delanzomib, marizomib, MG-132, ONX-0914, VR-23, celastrol, or epoxomicin.
20. The method of claim 18 , wherein said alkylating agent is cisplatin or carboplatin.
21. The method of claim 17 , wherein said compound is administered in a dose amount ranging from about 0.03 to about 10 mg, expressed as free base.
22. The method of claim 17 , wherein said compound is administered externally to the central nervous system.