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A lead compound for the development of ABA 8'-hydroxylase inhibitors
Authors:Ueno Kotomi  Yoneyama Hidetaka  Saito Shigeki  Mizutani Masaharu  Sakata Kanzo  Hirai Nobuhiro  Todoroki Yasushi
Institution:The United Graduate School of Agricultural Science, Gifu University, Gifu 501-1193, Japan.
Abstract:(1'S*,2'S*)-(+/-)-6-Nor-2',3'-dihydro-4'-deoxo-ABA (2) was designed and synthesized as a candidate lead compound for developing a potent and specific inhibitor of ABA 8'-hydroxylase. This compound acted as an effective competitive inhibitor of the enzyme, with a K(I) value of 0.40microM, without exhibiting ABA activity. However, compound 2 also functioned as an enzyme substrate, making it a short-lived inhibitor. The 8'-difluorinated derivative of 2 (4) was synthesized as a long-lasting alternative. Compound 4 resisted 8'-hydroxylation, but inhibited ABA 8'-hydroxylation as effectively as 2. These results suggest that compound 2 is a useful lead compound for the future design and development of an ideal ABA 8'-hydroxylase inhibitor.
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