5377-40-2Relevant articles and documents
Synthesis and evaluation of new N6-substituted adenosine-5′-N-methylcarboxamides as A3 adenosine receptor agonists
Devine, Shane M.,Gregg, Alison,Figler, Heidi,McIntosh, Kate,Urmaliya, Vijay,Linden, Joel,Pouton, Colin W.,White, Paul J.,Bottle, Steven E.,Scammells, Peter J.
experimental part, p. 3078 - 3087 (2010/07/08)
A number of N6-substituted adenosine-5′-N-methylcarboxamides were synthesised and their pharmacology, in terms of their receptor affinity, selectivity and cardioprotective effects, were explored. The first series of compounds, 4a-4f and 5a-5f,
Synthesis and inhibitory activity of alkyl(hydroxyaryl)amines
Dyubchenko,Nikulina,Terakh,Prosenko,Grigor'ev
, p. 1149 - 1155 (2008/09/17)
The reaction of ω-(4-hydroxyaryl)haloalkanes with various nitrogen-containing agents afforded primary, secondary, and tertiary amino derivatives of 2,6-dialkylphenols. For the compounds synthesized, the reaction rate constants with peroxide radicals were
3,5-disubstituted-4-hydroxyphenyls linked to 3-hydroxy-2-methyl-4(1h)- pyridinone: Potent inhibitors of lipid peroxidation and cell toxicity
Bebbington, David,Monck, Nathaniel J. T.,Gaur, Suneel,Palmer, Alan M.,Benwell, Karen,Harvey, Victoria,Malcolm, Craig S.,Porter, Richard H. P.
, p. 2779 - 2782 (2007/10/03)
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