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Inhibitors of histone methylation
Authors:M Cory  D W Henry  D L Taylor  K J Koskela
Institution:Bio-OrganIc Chemistry Department, Stanford Research Institute, Menlo Park, Calif. 94025 U.S.A.
Abstract:Two classes of inhibitors of histone methyltransferase I from calf thymus are reported. High concentrations (≧ 10 mM) 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. S-Adenosyl-l-ethionine (SAM) showed competitive inhibition of the enzyme as determined from a Lineweaver-Burke plot, while ethidium bromide was noncompetitive.
Keywords:SAM  TCA  trichloroacetic acid
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