1986 年 50 巻 9 号 p. 2243-2249
ω-Phenylalkyl derivatives of N6-substituted adenine, N6-substituted adenosine and 6-alkoxypurine with odd numbers of methylenes had relatively high activity, while the corresponding 2-methyl-4-substituted-aminopyrido[3, 4-d]pyrimidines with even numbers of methylenes had high activity in an Amaranthus betacyanin test and lettuce seed germination test. These results suggest that the ω-phenyl groups of the cytokinins play a specific role for cytokinin-receptor binding and that the pyrido[3, 4-d]pyrimidines interact with a receptor in a different binding mode.
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