Abstract
7-Substituted-5-aryl-pyrrolo[2,3-d]pyrimidines have been prepared starting from alpha-bromoacetophenones. These compounds represent a novel class of potent inhibitors of the tyrosine kinase pp60(c-Src) with good specificity towards other tyrosine kinases (EGF-R, v-Abl).
MeSH terms
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Alkanes / chemical synthesis*
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Alkanes / chemistry
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Alkanes / pharmacology
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Enzyme Inhibitors / chemical synthesis*
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Enzyme Inhibitors / chemistry
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Enzyme Inhibitors / pharmacology
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ErbB Receptors / antagonists & inhibitors
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Oncogene Proteins v-abl / antagonists & inhibitors
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Pyrimidines / chemical synthesis*
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Pyrimidines / chemistry
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Pyrimidines / pharmacology
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Pyrroles / chemical synthesis*
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Pyrroles / chemistry
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Pyrroles / pharmacology
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Structure-Activity Relationship
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src-Family Kinases / antagonists & inhibitors*
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src-Family Kinases / metabolism
Substances
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Alkanes
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Enzyme Inhibitors
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Oncogene Proteins v-abl
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Pyrimidines
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Pyrroles
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ErbB Receptors
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src-Family Kinases