Search Results - "VOLLINGA, Roel C."

N 6 ,5‘-Disubstituted Adenosine Derivatives as Partial Agonists for the Human Adenosine A 3 Receptor by van Tilburg, Erica W., von Frijtag Drabbe Künzel, Jacobien, de Groote, Miriam, Vollinga, Roel C., Lorenzen, Anna, IJzerman, Ad P.

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N6,5‘-Disubstituted Adenosine Derivatives as Partial Agonists for the Human Adenosine A3 Receptor by VAN TILBURG, Erica W., VON FRIJTAG DRABBE KüNZEL, Jacobien, DE GROOTE, Miriam, VOLLINGA, Roel C., LORENZEN, Anna, IJZERMAN, Ad P.

“…5'-(Alkylthio)-substituted analogues of N6-benzyl- and N6-(3-iodobenzyl)adenosine were synthesized in 37-61% overall yields. The affinities of these compounds…”
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Potent antagonists for the human adenosine A2B receptor. Derivatives of the triazolotriazine adenosine receptor antagonist ZM241385 with high affinity by de Zwart, Maarten, Vollinga, Roel C., Beukers, Margot W., Sleegers, Danielle F., von Frijtag Drabbe Künzel, Jacobien K., de Groote, Miriam, Ijzerman, Ad P.

“…A series of novel and known 5‐substituted 7‐amino‐2‐(2‐furyl)[1,2,4]triazolo[1,5‐a][1,3,5]triazine derivatives were synthesized and tested for adenosine…”
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N 6,5‘-Disubstituted Adenosine Derivatives as Partial Agonists for the Human Adenosine A3 Receptor by van Tilburg, Erica W, von Frijtag Drabbe Künzel, Jacobien, de Groote, Miriam, Vollinga, Roel C, Lorenzen, Anna, IJzerman, Ad P

“…5‘-(Alkylthio)-substituted analogues of N 6-benzyl- and N 6-(3-iodobenzyl)adenosine were synthesized in 37−61% overall yields. The affinities of these…”
Get full text