The pyrrolidine derivatives are GlyT1 inhibitors.
The present invention is furthermore related to novel pyrrolidine esters.
Also disclosed are novel intermediates useful for the preparation of the aforementioned pyrrolidine derivatives, as well as to methods for preparing both the intermediates and the final pyrrolidine derivatives.
The present invention is related to pyrrolidine oxadiazole and thiadiazole derivatives for use as pharmaceutically active compounds, as well as pharmaceutical formulations containing such pyrrolidine oxadiazole derivatives.
The invention relates to (among other things) oligomer-containing pyrrolidine compounds.
Substantially entiomerically pure 3,3-disubstituted-5-monosubstituted pyrrolidin-2-ones of formula (I) in which R2 is hydrogen and R and R1 are as defined in the description, are useful chiral auxiliaries for the synthesis of chiral molecules.
One was obtained by hydroxylation of the pyrrolidone ring (1.6% of the dose) and the other one by opening of the pyrrolidone ring (0.9% of the dose).
One was obtained by hydroxylation of the pyrrolidone ring (1.6 % of the dose) and the other one by opening of the pyrrolidone ring (0.9 % of the dose).
One was obtained by hydroxylation of the pyrrolidone ring (1.6 % of the dose) and the other one by opening of the pyrrolidone ring (0.9 % of the dose).
One was obtained by hydroxylation of the pyrrolidone ring (1.6 % of the dose) and the other one by opening of the pyrrolidone ring (0.9 % of the dose).
A novel pyrrolidine derivative represented by the formula (I) or a salt thereof.
One was obtained by hydroxylation of the pyrrolidone ring (1.6% of the dose) and the other one by opening of the pyrrolidone ring (0.9% of the dose).
A novel class of substituted homopiperidin, piperidine and pyrrolidine derivatives, methods for their preparation, pharmaceutical compositions comprising them and use thereof in the treatment of disorders related to the histamine H3 receptor.
One was obtained by hydroxylation of the pyrrolidone ring (1.6% of the dose) and the other one by opening of the pyrrolidone ring (0.9% of the dose).
This invention relates to a novel solid phase process for the preparation of pyrrolidine combinatorial libraries.
The diazatricycloalkanes typically consist of a 1-azabicyclooctane fused to pyrrolidine ring.
Bicyclic and tricyclic pyrrolidine derivatives are disclosed that are useful as antagonists of the GnRH receptor.
The present invention also relates to pharmaceutical compositions comprising pyrτoIidine-2,5-dione compounds.
The present invention relates to the use of 2-oxo-1-pyrrolidine derivatives (and in particular (S)-(-)-α-ethyl-2-oxo-1-pyrrolidineacetamide) for the preparation of drugs for the curative and/or prophylactic treatment of dyskinesia
No free pyrrolidine will be detected in the urine.
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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