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Synthesis of DHPA analogs and their inhibitory activities of human recombinant S-adenosyl-L-homocysteine hydrolase
Authors:Y Kitade  M Nakanishi  A Hosoya  A Hiraoka  M Hayashi  K Mori  T Gotoh  C Yatome
Affiliation:Department of Biomolecular Science, Faculty of Engineering, Gifu University, Japan.
Abstract:We report syntheses of DHPA analogs, e.g., 9-(3-formyl-2,3-dihydroxypropyl)adenine (FDHPA) and 9-(3-formyl-2,3-dihydroxypropyl)hypoxanthine (FDHPI). Among these DHPA analogs, FDHPA behaved as an irreversible inactivator of human recombinant SAH hydrolase.
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