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Targeting “Hydrolytic” Activity of the S-Adenosyl-L- Homocysteine Hydrolase

[ Vol. 1 , Issue. 3 ]


S. F. Wnuk   Pages 307 - 316 ( 10 )


Substrates that are specific for the hydrolytic activities of AdoHcy hydrolase have been recently identified. Upon interaction with the AdoHcy hydrolase such substrates generate the active electrophiles which then react with the enzyme nucleophiles to produce covalent inhibition. Dihalohomovinyl and haloacetylene analogues derived from adenosine as well 5-S-allenyl-5 -thioadenosine derivative have been characterized as the first type II mechanism-based inhibitors of AdoHcy hydrolase that rely only on the hydrolytic activity. Design and synthesis of the novel adenine nucleosides as well their interaction with AdoHcy hydrolase are discussed in this review


Hydrolytic Activity, S-Adenosyl-L-Homocysteine Hydrolase, Dihalovinyl Homoadenosine Analogues, Acetylene, Haloacetylene Analogues, Thioadenosine Derivatives


Department of Chemistry, Florida International University, Miami, Florida 33199, USA

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