SPALLUTO, GIAMPIERO

SPALLUTO, GIAMPIERO

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Dettaglio

SPALLUTO, GIAMPIERO 

Dipartimento di Scienze Chimiche e Farmaceutiche 

Settore CHIM/08 - Chimica Farmaceutica 

Docenti di ruolo di Ia fascia 

UnityFVG

7003738451

Pubblicazioni

Risultati 1 - 20 di 122 (tempo di esecuzione: 0.0 secondi).

TitoloData di pubblicazioneAutoriFile
11,2,4-Triazolo[1,5-a]-1,3,5-triazine nucleus: a possible template for adenosine receptor subtypes.2011FEDERICO, STEPHANIE  ; MORO, STEFANO  ; SPALLUTO, GIAMPIERO  -
2[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 Subtype2013FEDERICO, STEPHANIE  ; SPALLUTO, GIAMPIERO  -
3[1,2,4]Triazolo[1,5-c]pyrimidine Nucleus as Adenosine Receptor Antagonists: Shift in Selectivity from A2A to A3 Adenosine Receptors.2012FEDERICO, STEPHANIE  ; SPALLUTO, GIAMPIERO  -
4[1,2,4]triazolo[1,5-c]pyrimidines as A(3) adenosine receptor antagonists2014FEDERICO, STEPHANIE  ; REDENTI, SARA  ; SPALLUTO, GIAMPIERO  -
5[1,2,4]Triazolo[1,5-c]pyrimidines as adenosine receptor antagonists: Modifications at the 8 position to reach selectivity towards A3 adenosine receptor subtype2018FEDERICO, STEPHANIE  ; SPALLUTO, GIAMPIERO    Solo autorizzati
61,2,4]Triazolo[1,5-c]pyrimidines as New Potent Human A3 Adenosine Receptor Antagonists.2013SPALLUTO, GIAMPIERO  ; FEDERICO, STEPHANIE  ; -
7[3H]MRE 3008-F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A3 adenosine receptors.2000SPALLUTO, GIAMPIERO  ; -
85,7-Disubstituted-[1,2,4]triazolo[1,5-a][1,3,5]triazines as pharmacological tools to explore the antagonist selectivity profiles toward adenosine receptors2016FEDERICO, STEPHANIE  ; REDENTI, SARA  ; SPALLUTO, GIAMPIERO    Open Access
95-Alkylamino-pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidines. Influence of the Substituent on the Affinity at the Adenosine Receptor Subtypes2011FEDERICO, STEPHANIE  ; SPALLUTO, GIAMPIERO  -
10. 6-Amino-2-mercapto-3H-pyrimidin-4-one derivatives as new candidates for the antagonism at the P2Y12 receptors2009SPALLUTO, GIAMPIERO  ; -
117-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 solubility2002SPALLUTO, GIAMPIERO  ; -
128-(2-Furyl)adenine derivatives as A2A adenosine receptor ligands2013FEDERICO, STEPHANIE  ; SPALLUTO, GIAMPIERO  ; -
13A facile and versatile route to the synthesis of fused 2-pyridones: Useful intermediates for policyclic systems2006SPALLUTO, GIAMPIERO  -
14A new Multi-charged C60 Derivative: Synthesis and Biological Properties2002DA ROS, TATIANA  ; SPALLUTO, GIAMPIERO  ; PRATO, MAURIZIO  -
15A2Aadenosine receptor antagonists as therapeutic candidates: Are they still an interesting challenge?2018SPALLUTO, GIAMPIERO  ; FEDERICO, STEPHANIE    riservati
16A2B Adenosine Receptor Antagonists: Recent Developments2005SPALLUTO, GIAMPIERO  ; -
17A3 Adenosine receptor antagonistsdelay irreversible synaptic failure caused by oxygen and glucose deprivation in the rat CA1 hippocampus in vitro2006SPALLUTO, GIAMPIERO  ; -
18The A3 adenosine receptor as multifaceted therapeutic Target: pharmacology, medicinal Chemistry, and In silico approaches2013FEDERICO, STEPHANIE  ; SPALLUTO, GIAMPIERO  ;  riservati
19Advances in Computational Techniques to Study GPCR-Ligand Recognition2015FEDERICO, STEPHANIE  ; SPALLUTO, GIAMPIERO  ;  riservati
20ANTI-HIV PROPERTIES OF CATIONIC FULLERENE DERIVATIVES2005MARCHESAN, SILVIA  ; DA ROS, TATIANA  ; SPALLUTO, GIAMPIERO  ; PRATO, MAURIZIO  -
 
 
 
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