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J Med Chem ; 53(12): 4603-14, 2010 Jun 24.
Article in English | MEDLINE | ID: mdl-20491477

ABSTRACT

The GlyT1 transporter has emerged as a key novel target for the treatment of schizophrenia. Herein, we report on the optimization of the 2-alkoxy-5-methylsulfonebenzoylpiperazine class of GlyT1 inhibitors to improve hERG channel selectivity and brain penetration. This effort culminated in the discovery of compound 10a (RG1678), the first potent and selective GlyT1 inhibitor to have a beneficial effect in schizophrenic patients in a phase II clinical trial.


Subject(s)
Glycine Plasma Membrane Transport Proteins/antagonists & inhibitors , Piperazines/chemical synthesis , Psychotropic Drugs/chemical synthesis , Schizophrenia/drug therapy , Sulfones/chemical synthesis , Animals , Brain/metabolism , CHO Cells , Cricetinae , Cricetulus , ERG1 Potassium Channel , Ether-A-Go-Go Potassium Channels/antagonists & inhibitors , Humans , Macaca fascicularis , Male , Mice , Microdialysis , Motor Activity/drug effects , Patch-Clamp Techniques , Piperazines/pharmacokinetics , Piperazines/pharmacology , Psychotropic Drugs/pharmacokinetics , Psychotropic Drugs/pharmacology , Rats , Rats, Sprague-Dawley , Stereoisomerism , Structure-Activity Relationship , Sulfones/pharmacokinetics , Sulfones/pharmacology
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