Inhibition of S-Adenosylmethionine Decarboxylase from Rat Liver by Synthetic Decarboxylated S-Adenosylmethionine and Its Analogs
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Synthetic decarboxylated S-adenosylmethionine and six analogs were tested in a decarboxylating system based on rat liver S-adenosylmethionine decarboxylase. All the compounds inhibited the putrescine-activated decarboxylase activity and were competitive with respect to S-adenosylmethionine. Among the compounds tested, S-5'-deoxyadenos-yl-(5')-2-methylthioethylamine was the most potent inhibitor. The K_i value of the inhibitor was seven times lower than that of decarboxylated S-adenosylmethionine.
- 公益社団法人日本薬学会の論文
- 1980-07-25
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