Inhibitors of histone methylation |
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Authors: | M Cory D W Henry D L Taylor K J Koskela |
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Affiliation: | Bio-OrganIc Chemistry Department, Stanford Research Institute, Menlo Park, Calif. 94025 U.S.A. |
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Abstract: | Two classes of inhibitors of histone methyltransferase I from calf thymus are reported. High concentrations () of various alkyl or aralkyl amines and polyamines were inhibitory to the enzyme. Spermine and spermidine were among the most potent compounds in this group. The best monoamine inhibitor was 2-phenylethylamine, which gave 47% inhibition at 10 mM.The substituted phenanthridinium compound ethidium bromide was also an inhibitor of the enzyme. A number of analogs of ethidium bromide were tested, and the most potent compound (17) gave 50% inhibition at 0.125 mM. (SAM) showed competitive inhibition of the enzyme as determined from a Lineweaver-Burke plot, while ethidium bromide was noncompetitive. |
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Keywords: | SAM TCA trichloroacetic acid |
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