Abstract
A series of novel N-cyanoguanidine tricyclic farnesyl protein transferase (FPT) inhibitors was prepared. Replacement of a piperidine amide-group with a N-cyanoguanidine functionality increased FPT activity. X-ray crystal structure determination of 42 complexed with FPT revealed differences in the interactions of the amide and N-cyanoguanidine groups with the protein.
MeSH terms
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Alkyl and Aryl Transferases / antagonists & inhibitors*
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Crystallography, X-Ray
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Enzyme Inhibitors / chemical synthesis*
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Enzyme Inhibitors / pharmacology
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Guanidines / chemical synthesis*
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Guanidines / chemistry
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Guanidines / pharmacology*
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Heterocyclic Compounds, 4 or More Rings / chemical synthesis
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Heterocyclic Compounds, 4 or More Rings / chemistry
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Heterocyclic Compounds, 4 or More Rings / pharmacology
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Humans
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Inhibitory Concentration 50
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Molecular Structure
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Piperidines / chemical synthesis
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Piperidines / chemistry
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Piperidines / pharmacology
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Structure-Activity Relationship
Substances
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Enzyme Inhibitors
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Guanidines
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Heterocyclic Compounds, 4 or More Rings
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Piperidines
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Alkyl and Aryl Transferases
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p21(ras) farnesyl-protein transferase
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dicyandiamido