Abstract
The design and synthesis of a novel series of 2,6-disubstituted pyrazine derivatives as CK2 kinase inhibitors is described. Structure-guided optimization of a 5-substituted-3-thiophene carboxylic acid screening hit (3a) led to the development of a lead compound (12b), which shows inhibition in both enzymatic and cellular assays. Subsequent design and hybridization efforts also led to the unexpected identification of analogs with potent PIM kinase activity (14f).
Keywords:
2,6-Disubstituted pyrazine; Cancer; Dual CK2 and PIM kinase inhibitors.
Copyright © 2018 Elsevier Ltd. All rights reserved.
MeSH terms
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Casein Kinase II / antagonists & inhibitors*
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Cell Line, Tumor
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Drug Design
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Humans
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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 / pharmacokinetics
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Protein Kinase Inhibitors / pharmacology*
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Proto-Oncogene Proteins c-pim-1 / antagonists & inhibitors*
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Pyrazines / chemical synthesis
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Pyrazines / chemistry
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Pyrazines / pharmacokinetics
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Pyrazines / pharmacology*
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Structure-Activity Relationship
Substances
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Protein Kinase Inhibitors
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Pyrazines
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Casein Kinase II
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PIM1 protein, human
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Proto-Oncogene Proteins c-pim-1