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Design and Biological Evaluation of New Mechanismbased Inhibitors of S-Adenosyl-L-homocysteine Hydrolase
Authors:Stanislaw F. Wnuk  Chong-Sheng Yuan  Ronald T. Borchardt  J. Robins Morris
Affiliation:1. Department of Chemistry , Florida International University , Miami, FL, 33199;2. Department of Chemistry and Biochemistry , Brigham Young University , Provo, UT, 84602;3. Department of Biochemistry , University of Kansas , Lawrence, KS, 66047
Abstract:Abstract

Geminal dihalohomovinyl 2 and haloacetylenic 4 analogs derived from adenosine were prepared. These compounds exhibited type II (covalent) mechanism-based inactivation of S-adenosyl-L-homocysteine hydrolase.
Keywords:
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