| Literature DB >> 12781179 |
Katherine L Seley1, Stephen Quirk, Samer Salim, Liang Zhang, Asmerom Hagos.
Abstract
A series of shape-modified flexible nucleosides ('fleximers', 1, 2, and 3) was modeled, synthesized and subsequently assayed against S-adenosyl-L-homocysteine hydrolase (SAHase). No inhibitory activity was observed for the adenosine fleximer, which served as a substrate, but moderate inhibitory activity was exhibited by the guanosine fleximers. This is the first known report of a guanosine nucleoside analogue possessing activity against SAHase.Entities:
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Year: 2003 PMID: 12781179 DOI: 10.1016/s0960-894x(03)00331-7
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823