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SPALLUTO, GIAMPIERO

SPALLUTO, GIAMPIERO  

Dipartimento di Scienze Chimiche e Farmaceutiche  

Settore CHIM/08 - Chimica Farmaceutica  

Docenti di ruolo di Ia fascia  

UnityFVG

7003738451

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Risultati 1 - 20 di 130 (tempo di esecuzione: 0.032 secondi).
Titolo Data di pubblicazione Autori File
1,2,4-Triazolo[1,5-a]-1,3,5-triazine nucleus: a possible template for adenosine receptor subtypes. 1-gen-2011 FEDERICO, STEPHANIEMORO, STEFANOSPALLUTO, GIAMPIERO +
[1,2,4]Triazolo[1,5-a][1,3,5]Triazine Derivatives as Antagonists for the Adenosine Receptors: a Preliminary Study on Affinity at the A3 Subtype 1-gen-2013 FEDERICO, STEPHANIEMORO, STEFANOSPALLUTO, GIAMPIERO +
[1,2,4]Triazolo[1,5-c]pyrimidine Nucleus as Adenosine Receptor Antagonists: Shift in Selectivity from A2A to A3 Adenosine Receptors. 1-gen-2012 FEDERICO, STEPHANIEMORO, STEFANOSPALLUTO, GIAMPIERO +
[1,2,4]triazolo[1,5-c]pyrimidines as A(3) adenosine receptor antagonists 1-gen-2014 FEDERICO, STEPHANIEREDENTI, SARAMORO, STEFANOSPALLUTO, GIAMPIERO +
[1,2,4]Triazolo[1,5-c]pyrimidines as adenosine receptor antagonists: Modifications at the 8 position to reach selectivity towards A3 adenosine receptor subtype 1-gen-2018 Federico, StephanieSpalluto, Giampiero +
1,2,4]Triazolo[1,5-c]pyrimidines as New Potent Human A3 Adenosine Receptor Antagonists. 1-gen-2013 SPALLUTO, GIAMPIEROFEDERICO, STEPHANIEMORO, STEFANO +
[3H]MRE 3008-F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A3 adenosine receptors. 1-gen-2000 SPALLUTO, GIAMPIERO +
5,7-Disubstituted-[1,2,4]triazolo[1,5-a][1,3,5]triazines as pharmacological tools to explore the antagonist selectivity profiles toward adenosine receptors 1-gen-2016 FEDERICO, STEPHANIEREDENTI, SARASPALLUTO, GIAMPIERO +
5-Alkylamino-pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidines. Influence of the Substituent on the Affinity at the Adenosine Receptor Subtypes 1-gen-2011 FEDERICO, STEPHANIEMORO, STEFANOSPALLUTO, GIAMPIERO +
. 6-Amino-2-mercapto-3H-pyrimidin-4-one derivatives as new candidates for the antagonism at the P2Y12 receptors 1-gen-2009 SPALLUTO, GIAMPIERO +
7-Substituted-5-amino-2-(2-furyl)-pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidines as A2A adenosine receptor antagonists: a study on the importance of modifications at the side chain on the activity and solubility 1-gen-2002 SPALLUTO, GIAMPIERO +
8-(2-Furyl)adenine derivatives as A2A adenosine receptor ligands 1-gen-2013 FEDERICO, STEPHANIESPALLUTO, GIAMPIERO +
A facile and versatile route to the synthesis of fused 2-pyridones: Useful intermediates for policyclic systems 1-gen-2006 SPALLUTO, GIAMPIERO +
A new Multi-charged C60 Derivative: Synthesis and Biological Properties 1-gen-2002 DA ROS, TATIANASPALLUTO, GIAMPIEROPRATO, MAURIZIO +
A2Aadenosine receptor antagonists as therapeutic candidates: Are they still an interesting challenge? 1-gen-2018 Spalluto, GiampieroFederico, Stephanie +
A2B Adenosine Receptor Antagonists: Recent Developments 1-gen-2005 SPALLUTO, GIAMPIERO +
A3 Adenosine receptor antagonistsdelay irreversible synaptic failure caused by oxygen and glucose deprivation in the rat CA1 hippocampus in vitro 1-gen-2006 SPALLUTO, GIAMPIERO +
The A3 adenosine receptor as multifaceted therapeutic Target: pharmacology, medicinal Chemistry, and In silico approaches 1-gen-2013 FEDERICO, STEPHANIESPALLUTO, GIAMPIERO +
Advances in Computational Techniques to Study GPCR-Ligand Recognition 1-gen-2015 FEDERICO, STEPHANIESPALLUTO, GIAMPIERO +
ANTI-HIV PROPERTIES OF CATIONIC FULLERENE DERIVATIVES 1-gen-2005 MARCHESAN, SILVIADA ROS, TATIANASPALLUTO, GIAMPIEROPRATO, MAURIZIO +