Abstract
When located in the DNA minor groove, dimeric bisbenzimidazoles DB(n) effectively inhibited in vitro the Dnmt3a catalytic domain (IC₅₀ 5-77 μM). The lowest IC₅₀ value was observed for compound DB(11) with an 11-unit methylene linker joining the bisbenzimidazole fragments. Increased time of incubation of DNA with DB(n) as well as the presence of AT-clusters in DNA enhances the inhibitory effect.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Bisbenzimidazole / chemical synthesis
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Bisbenzimidazole / chemistry
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Bisbenzimidazole / pharmacology*
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Catalytic Domain
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DNA Methylation / drug effects*
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DNA Modification Methylases / chemistry*
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DNA Modification Methylases / metabolism*
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Magnetic Resonance Spectroscopy
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Mice
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Molecular Structure
Substances
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DNA Modification Methylases
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Bisbenzimidazole