Derivatives of glycinergic R(+)-2-amino-3-hydroxypropanoic acid
View Patent ↗The use of R(+)-2-amino-3-hydroxypropanoic acid derivatives, nitrogen substituted by a (C 1 -C 6 )alkyl, (C 3 -C 6 )alkenyl, 3-oxo(C 5 -C 6 )alkyl, 3-oxo(C 4 -C 6 )alken-2-yl, phenyl(C 1 -C 6 )alkyl, phenyl(C 2 -C 6 )alkenyl, gem-diphenyl(C 1 -C 6 )alkyl, gem-diphenyl(C 2 -C 6 )alkenyl, (C 1 -C 6 )alcanoyl, optionally N-substituted alanyl, optionally N,N′-disubstituted lysinoyl, phenyl(C 1 -C 6 )alkylydene or gem-diphenyl(C 1 -C 6 )alkylidene group, and of the pharmaceutically acceptable salts thereof, for preparation of medicaments intended for the treatment of CNS diseases due to reduced glycinergic transmission, particularly for the treatment of autism, schizophrenia and Alzheimer's disease, is described.
1. A R(+)-2-amino-3-hydroxypropanoic acid derivative of formula III, or one of its pharmaceutically acceptable salts;
wherein R is hydrogen;
R′ is hydrogen, or a phenyl(C 2 -C 6 )alkenyl group, or a gem-diphenyl(C 1 -C 6 )alkyl group other than benzhydryl, or a gem-diphenyl(C 2 -C 6 )alkenyl group; or
R and R′, together, form a phenyl(C 1 -C 6 )alkylidene or gem-diphenyl(C 1 -C 6 )alkylidene group;
R″ is hydrogen or a (C 1 -C 6 )alkyl, (C 3 -C 6 )cycloalkyl(C 1 -C 6 )alkyl, phenyl(C 1 -C 2 )alkyl or phenacetyl group;
the phenyl group or groups being non-substituted or substituted by a halogen atom or by a hydroxy, (C 1 -C 3 )alkoxy, cyano, nitro or acetyl group;
with the proviso that, when R and R′ are both hydrogen, then R″ is other than hydrogen, (C 1 -C 6 )alkyl or non-substituted benzyl.
2. The R(+)-2-amino-3-hydroxypropanoic acid derivative according to claim 1 , where R′ is a ω-diphenyl(C 2 -C 6 )alkyl group.
3. R(+)-N-(4,4-diphenyl)butyl-2-amino-3-hydroxypropanoic acid or a pharmaceutically acceptable salt thereof.
4. R(+)-N-[(4,4-diphenyl)-3-butenyl]-2-amino-3-hydroxypropanoic acid or a pharmaceutically acceptable salt thereof.
5. R(+)-N-[α-phenyl-(2-hydroxy)benzylidene]-2-amino-3-hydroxypropanoic acid or a pharmaceutically acceptable salt thereof.
6. A method for treating schizophrenia, comprising administering to a patient the R(+)-2-amino-3-hydroxypropanoic acid derivative according to claim 1 .
7. The method according to claim 6 , wherein said treatment increases glycinergic transmission in said patient.
8. The R(+)-2-amino-3-hydroxypropanoic acid derivative according to claim 1 , wherein R′ is a phenyl(C 2 -C 6 )alkenyl.
9. The R(+)-2-amino-3-hydroxypropanoic acid derivative according to claim 1 , which is R(+)-N-(4,4-diphenyl)butyl-2-amino-3-hydroxypropanoic acid hydrochloride.
10. The R(+)-2-amino-3-hydroxypropanoic acid derivative according to claim 1 , which is methyl R(+)-N-[(4,4-diphenyl)-3-butenyl]-2-amino-3-hydroxypropanoate.
11. A pharmaceutical composition comprising a pharmaceutically effective dose of the R(+)-2-amino-3-hydroxypropanoic acid derivative according to claim 1 , or one of its pharmaceutically acceptable salts, in admixture with a pharmaceutically acceptable carrier.