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Synthesis and Biological Activities of 8'-Methylene- and 8'-Methylidyneabscisic Acids
Y Todoroki1, S Nakano1, S Arai1
1a Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University , Kitashirakawa-oiwake-cho, Sakyo-ku, Kyoto 606-01 , Japan.
Abstract:
8'-Methylene- and 8'-methylidyneabscisic acids which might act as suicide inhibitors of the 8'-hydroxylase of abscisic acid, were designed, synthesized, and optically resolved. The (+)-isomers showed stronger inhibitory activity in rice elongation and in lettuce seed germination than (+)-abscisic acid. The activity of (+)-8'-methylidyneabscisic acid was the strongest of the analogues synthesized to date, 40-fold stronger than abscisic acid.
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