Abstract
A rapid structure-activity study was performed by parallel liquid synthesis on N,N'-disubstitution of 3-amino azepin-2-one to afford potent and specific farnesyl transferase inhibitors with low nM enzymatic and cellular activities. The activities of the selected compounds were validated in vivo, and compounds 41a and 44a presented significant antitumour activity.
MeSH terms
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Alkyl and Aryl Transferases / antagonists & inhibitors*
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Amines / chemical synthesis
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Animals
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Antineoplastic Agents / chemical synthesis*
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Antineoplastic Agents / pharmacology
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Azepines / chemical synthesis*
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Azepines / pharmacology
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Cell Line, Tumor
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Drug Screening Assays, Antitumor
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Enzyme Inhibitors / chemical synthesis*
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Enzyme Inhibitors / pharmacology
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Farnesyltranstransferase
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Imidazoles / chemical synthesis
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Lactams / chemical synthesis
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Mice
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Molecular Structure
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Rats
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Structure-Activity Relationship
Substances
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Amines
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Antineoplastic Agents
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Azepines
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Enzyme Inhibitors
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Imidazoles
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Lactams
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imidazole
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Alkyl and Aryl Transferases
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Farnesyltranstransferase