Literature DB >> 14510356

Stereo-defined synthesis of 5'-(Z)-substituted 4',5'-unsaturated adenosines and evaluation of their inhibitory activity against S-adenosyl homocysteine hydrolase.

Hiroki Kumamoto1, Sayoko Onuma, Hiromichi Tanaka, Yukio Kitade.   

Abstract

A new approach was developed for the synthesis of 5'-(Z)-substituted 4',5'-unsaturated adenosines, potential inhibitors against S-adenosyl-L-homocysteine hydrolase (SAHase). A highly stereoselective radical-mediated sulfur-extrusive stannylation was employed as a key step in the present approach. Inhibitory activity of the compounds against SAHase is also presented.

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Year:  2003        PMID: 14510356     DOI: 10.1093/nass/3.1.13

Source DB:  PubMed          Journal:  Nucleic Acids Res Suppl


  1 in total

1.  Anionic cascade reactions. One-pot assembly of (Z)-chloro-exo-methylenetetrahydrofurans from β-hydroxyketones.

Authors:  István E Markó; Florian T Schevenels
Journal:  Beilstein J Org Chem       Date:  2013-07-03       Impact factor: 2.883

  1 in total

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