Abstract
A series of imidazo[1,2-a]pyridin-6-yl-benzamide analogs was designed as inhibitors of B-RAFV600E. Medicinal chemistry techniques were employed to explore the SAR for this series and improve selectivity versus P38 and VEGFR2.
Keywords:
Kinase; MAPK; RAF.
Copyright © 2017 Elsevier Ltd. All rights reserved.
MeSH terms
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Benzamides / chemical synthesis
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Benzamides / chemistry
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Benzamides / pharmacology*
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Dose-Response Relationship, Drug
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Heterocyclic Compounds, 2-Ring / chemical synthesis
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Heterocyclic Compounds, 2-Ring / chemistry
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Heterocyclic Compounds, 2-Ring / pharmacology*
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Humans
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Models, Molecular
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Molecular Structure
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Protein Kinase Inhibitors / chemical synthesis
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Protein Kinase Inhibitors / chemistry
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Protein Kinase Inhibitors / pharmacology*
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Proto-Oncogene Proteins B-raf / antagonists & inhibitors*
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Proto-Oncogene Proteins B-raf / metabolism
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Structure-Activity Relationship
Substances
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Benzamides
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Heterocyclic Compounds, 2-Ring
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Protein Kinase Inhibitors
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Proto-Oncogene Proteins B-raf