The Inhibition of Adenosine Kinase by α,ω-Di (Adenosin -N6- YL) Alkanes1
Author:
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/07328318908054174
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1. Inhibition of rabbit skeletal muscle adenylate kinase by the transition state analogue, P1,P4-di(adenosine-5′)tetraphosphate
2. P1,P5-Di(adenosine-5′)pentaphosphate, a Potent Multisubstrate Inhibitor of Adenylate Kinase
3. Synthetic Inhibitors of Adenylate Kinases in the Assays for ATPases and Phosphokinases
4. Inhibition of thymidine kinase by P1-(adenosine-5‘)-P5-(thymidine-5‘)-pentaphosphate.
5. Inhibition of adenosine and thymidylate kinases by bisubstrate analogs.
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1. Alkylation of 9-substituted guanine derivatives with α,ω-dihaloalkanes;Heteroatom Chemistry;2017-09
2. 5-(3-Bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[2,3-d]pyrimidin-4-ylamine: structure–activity relationships of 7-substituted heteroaryl analogs as non-nucleoside adenosine kinase inhibitors;Bioorganic & Medicinal Chemistry;2005-06
3. Adenosine Analogues as Inhibitors of Trypanosoma brucei Phosphoglycerate Kinase: Elucidation of a Novel Binding Mode for a 2-Amino-N6-Substituted Adenosine;Journal of Medicinal Chemistry;2000-10-12
4. Intrinsic tryptophan fluorescence of bovine liver adenosine kinase, characterization of ligand binding sites and conformational changes;European Journal of Biochemistry;1994-04
5. The bis(adenosin-N6-yl) alkanes, a family of potential dinucleoside polyphosphate analogue precursors. Mechanism of growth inhibition and suppression of adenosine toxicity in lymphoid cells;European Journal of Biochemistry;1993-07
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