Abstract
We describe here the discovery and biological profile of a series of isoindolinone derivatives as developed mGluR1 antagonists. Our combined strategy of rapid parallel synthesis and conventional medicinal optimization successfully led to N-cyclopropyl 22 and N-isopropyl isoindolinone analogs 21 and 23 with improved in vivo DMPK profiles. Moreover the most advanced analog 23 showed an oral antipsychotic-like effect at a dose of 1mg/kg in an animal model.
MeSH terms
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Animals
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Antipsychotic Agents / chemistry
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Antipsychotic Agents / pharmacology*
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Antipsychotic Agents / therapeutic use
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Hepatocytes / drug effects
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Humans
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Indoles / chemistry
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Indoles / pharmacology*
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Indoles / therapeutic use
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Mice
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Psychotic Disorders / drug therapy*
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Rats
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Receptors, Metabotropic Glutamate / antagonists & inhibitors*
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Receptors, Metabotropic Glutamate / metabolism*
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Structure-Activity Relationship
Substances
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Antipsychotic Agents
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Indoles
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Receptors, Metabotropic Glutamate
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metabotropic glutamate receptor type 1