Suchergebnisse - "Paoletta, Silvia"

PubPharm (13)

1

Species differences and mechanism of action of A3 adenosine receptor allosteric modulators

enthalten in: Purinergic signalling | 2018

von Du, L. | Gao, Z. | Paoletta, S. | +7

2

Structure-Activity Analysis of Biased Agonism at the Human Adenosine A3 Receptor

enthalten in: Molecular pharmacology | 2016

von Baltos, J. | Paoletta, S. | Nguyen, A. | +5

3

Photomodulation of G protein-coupled adenosine receptors by a novel light-switchable ligand

enthalten in: Bioconjugate chemistry | 2014

von Bahamonde, M. | Taura, J. | Paoletta, S. | +7

4

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

enthalten in: Bioorganic & medicinal chemistry | 2014

von Toti, K. | Moss, S. | Paoletta, S. | +3

5

Extended N(6) substitution of rigid C2-arylethynyl nucleosides for exploring the role of extracellular loops in ligand recognition at the A3 adenosine receptor

enthalten in: Bioorganic & medicinal chemistry letters | 2014

von Tosh, D. | Paoletta, S. | Chen, Z. | +4

6

Rational design of sulfonated A3 adenosine receptor-selective nucleosides as pharmacological tools to study chronic neuropathic pain

enthalten in: Journal of medicinal chemistry | 2013

von Paoletta, S. | Tosh, D. | Finley, A. | +6

7

Exploring the directionality of 5-substitutions in a new series of 5-alkylaminopyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine as a strategy to design novel human a(3) adenosine receptor antagonists

enthalten in: Journal of medicinal chemistry | 2012

von Federico, S. | Ciancetta, A. | Sabbadin, D. | +6

8

Discovery of novel A3 adenosine receptor ligands based on chromone scaffold

enthalten in: Biochemical pharmacology | 2012

von Gaspar, A. | Reis, J. | Kachler, S. | +5

9

Novel fluorescent antagonist as a molecular probe in A(3) adenosine receptor binding assays using flow cytometry

enthalten in: Biochemical pharmacology | 2012

von Kozma, E. | Kumar, T. | Federico, S. | +7

10

Does the combination of optimal substitutions at the C²-, N⁵- and N⁸-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A₃ adenosine receptors?

enthalten in: Bioorganic & medicinal chemistry | 2011

von Cheong, S. | Dolzhenko, A. | Paoletta, S. | +8