Abstract
We report the optimization of a series of non-MPEP site metabotropic glutamate receptor 5 (mGlu(5)) positive allosteric modulators (PAMs) based on a simple acyclic ether series. Modifications led to a gain of MPEP site interaction through incorporation of a chiral amide in conjunction with a nicotinamide core. A highly potent PAM, 8v (VU0404251), was shown to be efficacious in a rodent model of psychosis. These studies suggest that potent PAMs within topologically similar chemotypes can be developed to preferentially interact or not interact with the MPEP allosteric binding site.
Copyright © 2012 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Allosteric Regulation / drug effects*
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Allosteric Site / drug effects
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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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Ethers / chemistry
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Ethers / pharmacology
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Ethers / therapeutic use
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Humans
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Niacinamide / chemistry*
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Niacinamide / pharmacology*
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Niacinamide / therapeutic use
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Psychotic Disorders / drug therapy
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Rats
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Receptor, Metabotropic Glutamate 5
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Receptors, Metabotropic Glutamate / chemistry
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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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Ethers
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Receptor, Metabotropic Glutamate 5
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Receptors, Metabotropic Glutamate
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Niacinamide