Ghent University Academic Bibliography

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Assessment of biased agonism at the A(3) adenosine receptor using beta-arrestin and miniG alpha(i) recruitment assays

Eline Pottie (UGent) , Dilip K. Tosh, Zhan-Guo Gao, Kenneth A. Jacobson and Christophe Stove (UGent)

(2020) BIOCHEMICAL PHARMACOLOGY. 177.
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Probing structure-activity relationship in beta-arrestin2 recruitment of diversely substituted adenosine derivatives

Jolien Storme, Dilip K Tosh, Zhan-Guo Gao, Kenneth A Jacobson and Christophe Stove (UGent)

(2018) BIOCHEMICAL PHARMACOLOGY. 158. p.103-113
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- Journal Article
- A1
- open access
Synthesis and evaluation of N⁶-substituted apioadenosines as potential adenosine A₃ receptor modulators

Kiran Toti (UGent) , Steven M Moss, Silvia Paoletta, Zhan-Guo Gao, Kenneth A Jacobson and Serge Van Calenbergh (UGent)

(2014) BIOORGANIC & MEDICINAL CHEMISTRY. 22(15). p.4257-4268
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- Journal Article
- A1
- open access
2-Triazole-substituted adenosines: a new class of selective A₃ adenosine receptor agonists, partial agonists, and antagonists

Liesbet Cosyn (UGent) , Krishnan K Palaniappan, Soo-Kyung Kim, Heng T Duong, Zhan-Guo Gao, Kenneth A Jacobson and Serge Van Calenbergh (UGent)

(2006) JOURNAL OF MEDICINAL CHEMISTRY. 49(25). p.7373-7383
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Exploring human adenosine A₃ receptor complementarity and activity for adenosine analogues modified in the ribose and purine moiety

Philippe Van Rompaey (UGent) , Kenneth A Jacobson, Ariel S Gross, Zhan-Guo Gao and Serge Van Calenbergh (UGent)

(2005) BIOORGANIC & MEDICINAL CHEMISTRY. 13(4). p.973-983

Academic Bibliography

Assessment of biased agonism at the A(3) adenosine receptor using beta-arrestin and miniG alpha(i) recruitment assays

Probing structure-activity relationship in beta-arrestin2 recruitment of diversely substituted adenosine derivatives

Synthesis and evaluation of N⁶-substituted apioadenosines as potential adenosine A₃ receptor modulators

2-Triazole-substituted adenosines: a new class of selective A₃ adenosine receptor agonists, partial agonists, and antagonists

Exploring human adenosine A₃ receptor complementarity and activity for adenosine analogues modified in the ribose and purine moiety

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