Abstract
Herein we report a next generation muscarinic receptor 4 (M(4)) positive allosteric modulator (PAM), ML253 which exhibits nanomolar activity at both the human (EC(50)=56 nM) and rat (EC(50)=176 nM) receptors and excellent efficacy by the left-ward shift of the ACh concentration response curve (fold shift, human=106; rat=50). In addition, ML253 is selective against the four other muscarinic subtypes, displays excellent CNS exposure and is active in an amphetamine-induced hyperlocomotion assay.
Copyright © 2012 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Allosteric Regulation
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Amides / chemistry*
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Amides / pharmacokinetics
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Amides / therapeutic use
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Animals
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Brain / drug effects
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Brain / metabolism*
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Cholinergic Agents / chemistry
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Cholinergic Agents / pharmacokinetics
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Cholinergic Agents / therapeutic use
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Disease Models, Animal
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Drug Evaluation, Preclinical
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Half-Life
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Humans
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Protein Binding
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Pyridines / chemistry*
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Pyridines / pharmacokinetics
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Pyridines / therapeutic use
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Rats
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Receptor, Muscarinic M4 / chemistry
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Receptor, Muscarinic M4 / metabolism*
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Schizophrenia / drug therapy
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Structure-Activity Relationship
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Thiophenes / chemistry*
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Thiophenes / pharmacokinetics
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Thiophenes / therapeutic use
Substances
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Amides
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Cholinergic Agents
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ML253
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Pyridines
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Receptor, Muscarinic M4
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Thiophenes
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pyridine