Abstract
A multidimensional, iterative parallel synthesis effort identified a series of highly selective mGlu3 NAMs with submicromolar potency and good CNS penetration. Of these, ML337 resulted (mGlu3 IC50 = 593 nM, mGlu2 IC50 >30 μM) with B:P ratios of 0.92 (mouse) to 0.3 (rat). DMPK profiling and shallow SAR led to the incorporation of deuterium atoms to address a metabolic soft spot, which subsequently lowered both in vitro and in vivo clearance by >50%.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Allosteric Regulation / drug effects
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Animals
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Brain / drug effects
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Brain / metabolism*
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Drug Discovery*
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Humans
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Inhibitory Concentration 50
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Mice
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Piperidines / chemistry
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Piperidines / metabolism*
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Piperidines / pharmacokinetics
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Piperidines / pharmacology*
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Rats
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Receptors, Metabotropic Glutamate / chemistry*
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Receptors, Metabotropic Glutamate / metabolism*
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Substrate Specificity
Substances
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(R)-(2-fluoro-4-((-4-methoxyphenyl)ethynyl)phenyl)(3-hydroxypiperidin-1-yl)methanone
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Piperidines
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Receptors, Metabotropic Glutamate
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metabotropic glutamate receptor 3