Abstract
Novel conformationally-restricted mTOR kinase inhibitors with cyclic sulfone scaffold were designed. Synthesis and structure-activity relationship (SAR) studies are described with emphasis on optimization of the mTOR potency and selectivity against class I PI3Kα kinase. PF-05139962 was identified with excellent mTOR biochemical inhibition, cellular potency, kinase selectivity and in vitro ADME properties.
Copyright © 2012 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Binding Sites
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Computer Simulation
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Half-Life
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Humans
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Microsomes, Liver / metabolism
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Morpholines / chemical synthesis
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Morpholines / chemistry*
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Morpholines / pharmacokinetics
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Phosphatidylinositol 3-Kinases / metabolism
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Phosphoinositide-3 Kinase Inhibitors
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Protein Kinase Inhibitors / chemical synthesis
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Protein Kinase Inhibitors / chemistry*
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Protein Kinase Inhibitors / pharmacokinetics
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Protein Structure, Tertiary
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Rats
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Structure-Activity Relationship
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Sulfones / chemical synthesis
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Sulfones / chemistry*
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Sulfones / pharmacokinetics
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TOR Serine-Threonine Kinases / antagonists & inhibitors*
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TOR Serine-Threonine Kinases / metabolism
Substances
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Morpholines
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PF-05139962
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Phosphoinositide-3 Kinase Inhibitors
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Protein Kinase Inhibitors
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Sulfones
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TOR Serine-Threonine Kinases