Department of Botany, The University of Kansas, Lawrence, Kansas 66044.
Plant Physiol. 1971 Feb;47(2):275-81. doi: 10.1104/pp.47.2.275.
In order to test the metabolic stability of 9-substituted cytokinins, 6-benzylamino-9-methyl purine has been synthesized and labeled with (14)C in the 9-methyl carbon or doubly labeled with (14)C in the 9-methyl carbon and (3)H in the methylene moiety of the side chain. Although the 6-benzylamino-9-methylpurine is chemically stable, cytokinin-requiring tissues begin removing the 9-substituent in as little as 10 minutes. Among the various metabolic products is free benzylaminopurine. Thus, the biological activity of 9-substituted cytokinins could be accounted for by their conversion to the free base.
为了测试 9-取代细胞分裂素的代谢稳定性,已经合成了 6-苄氨基-9-甲基嘌呤,并在 9-甲基碳上用 (14)C 标记或在侧链的亚甲基部分用 (14)C 和 (3)H 双重标记。尽管 6-苄氨基-9-甲基嘌呤在化学上是稳定的,但需要细胞分裂素的组织在短短 10 分钟内就开始去除 9-取代基。在各种代谢产物中,有游离的苄氨基嘌呤。因此,9-取代细胞分裂素的生物活性可以归因于它们转化为游离碱。