Design, synthesis, and binding of homologated truncated 4'-thioadenosine derivatives at the human A3 adenosine receptors
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Synthesis and Binding Affinity of Homologated Adenosine Analogues as A3 Adenosine Receptor Ligands.Click modification in the N6 region of A3 adenosine receptor-selective carbocyclic nucleosides for dendrimeric tethering that preserves pharmacophore recognition.Syntheses of sulfur and selenium analogues of pachastrissamine via double displacements of cyclic sulfate.
P2860
Design, synthesis, and binding of homologated truncated 4'-thioadenosine derivatives at the human A3 adenosine receptors
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 14 August 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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Design, synthesis, and binding ...... e human A3 adenosine receptors
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Design, synthesis, and binding ...... human A3 adenosine receptors.
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type
label
Design, synthesis, and binding ...... e human A3 adenosine receptors
@en
Design, synthesis, and binding ...... human A3 adenosine receptors.
@nl
prefLabel
Design, synthesis, and binding ...... e human A3 adenosine receptors
@en
Design, synthesis, and binding ...... human A3 adenosine receptors.
@nl
P2093
P2860
P1476
Design, synthesis, and binding ...... e human A3 adenosine receptors
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P2093
Hea Ok Kim
Hyuk Woo Lee
Jin Hee Lee
Kenneth A Jacobson
Lak Shin Jeong
Seul-gi Park
Won Jun Choi
P2860
P304
P356
10.1016/J.BMC.2010.08.018
P407
P577
2010-08-14T00:00:00Z