2-triazole-substituted adenosines: a new class of selective A3 adenosine receptor agonists, partial agonists, and antagonists.
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Translocation of arrestin induced by human A(3) adenosine receptor ligands in an engineered cell line: comparison with G protein-dependent pathways2-Dialkynyl derivatives of (N)-methanocarba nucleosides: 'Clickable' A(3) adenosine receptor-selective agonists.Copper(I)-catalyzed cycloaddition of silver acetylides and azides: incorporation of volatile acetylenes into the triazole core.Functionalized congeners of A3 adenosine receptor-selective nucleosides containing a bicyclo[3.1.0]hexane ring system.Structure-Based Design, Synthesis by Click Chemistry and in Vivo Activity of Highly Selective A3 Adenosine Receptor Agonists.Structure-guided design of A(3) adenosine receptor-selective nucleosides: combination of 2-arylethynyl and bicyclo[3.1.0]hexane substitutions.Medicinal chemistry of the A3 adenosine receptor: agonists, antagonists, and receptor engineering.Synthesis and biological properties of C-2 triazolylinosine derivatives.Design of (N)-methanocarba adenosine 5'-uronamides as species-independent A3 receptor-selective agonists.Cu(I)-catalyzed Huisgen azide-alkyne 1,3-dipolar cycloaddition reaction in nucleoside, nucleotide, and oligonucleotide chemistry.Inhibition of siderophore biosynthesis by 2-triazole substituted analogues of 5'-O-[N-(salicyl)sulfamoyl]adenosine: antibacterial nucleosides effective against Mycobacterium tuberculosisThe A3 adenosine receptor as multifaceted therapeutic target: pharmacology, medicinal chemistry, and in silico approaches.A3 Adenosine Receptors as Modulators of Inflammation: From Medicinal Chemistry to Therapy.Synthesis of purine modified 2'-C-methyl nucleosides as potential anti-HCV agents.Strain Promoted Click Chemistry of 2- or 8-Azidopurine and 5-Azidopyrimidine Nucleosides and 8-Azidoadenosine Triphosphate with Cyclooctynes. Application to Living Cell Fluorescent Imaging.Steering the azido-tetrazole equilibrium of 4-azidopyrimidines via substituent variation - implications for drug design and azide-alkyne cycloadditions.Azide-tetrazole equilibrium of C-6 azidopurine nucleosides and their ligation reactions with alkynesAzidophenyl as a click-transformable redox label of DNA suitable for electrochemical detection of DNA-protein interactions.ADP-ribosyl-N₃: A Versatile Precursor for Divergent Syntheses of ADP-ribosylated Compounds.
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P2860
2-triazole-substituted adenosines: a new class of selective A3 adenosine receptor agonists, partial agonists, and antagonists.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on December 2006
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
2-triazole-substituted adenosi ...... ial agonists, and antagonists.
@en
2-triazole-substituted adenosi ...... ial agonists, and antagonists.
@nl
type
label
2-triazole-substituted adenosi ...... ial agonists, and antagonists.
@en
2-triazole-substituted adenosi ...... ial agonists, and antagonists.
@nl
prefLabel
2-triazole-substituted adenosi ...... ial agonists, and antagonists.
@en
2-triazole-substituted adenosi ...... ial agonists, and antagonists.
@nl
P2093
P2860
P50
P356
P1476
2-triazole-substituted adenosi ...... ial agonists, and antagonists.
@en
P2093
Heng T Duong
Krishnan K Palaniappan
Liesbet Cosyn
Soo-Kyung Kim
P2860
P304
P356
10.1021/JM0608208
P407
P577
2006-12-01T00:00:00Z