REDENTI, SARA

REDENTI, SARA  

Dipartimento di Scienze Chimiche e Farmaceutiche  

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Risultati 1 - 12 di 12 (tempo di esecuzione: 0.023 secondi).
Titolo Data di pubblicazione Autori File
[1,2,4]triazolo[1,5-c]pyrimidines as A(3) adenosine receptor antagonists 1-gen-2014 FEDERICO, STEPHANIEREDENTI, SARAMORO, STEFANOSPALLUTO, 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 +
Conjugable A3 Adenosine Receptor Antagonists: Probing the 5 Position of the Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine Scaffold. 1-gen-2014 FEDERICO, STEPHANIEREDENTI, SARAMORO, STEFANOSPALLUTO, GIAMPIERO +
CVT 6975-like Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine Derivatives: an Attempt towards A2B Adenosine Receptor Affinity. 1-gen-2014 REDENTI, SARAFEDERICO, STEPHANIEMORO, STEFANOSPALLUTO, GIAMPIERO +
DESIGN, SYNTHESIS AND CHARACTERIZATION OF GSK-3β AND CK-1δ INHIBITORS 4-mag-2017 REDENTI, SARA
Developing novel classes of protein kinase CK1δ inhibitors by fusing [1,2,4]triazole with different bicyclic heteroaromatic systems 1-gen-2021 Grieco I.Redenti S.Spalluto G.Federico S. +
The Influence of the 1-(3-Trifluoromethyl-Benzyl)-1H-Pyrazole-4-yl Moiety on the Adenosine Receptors Affinity Profile of Pyrazolo[4,3-e][1,2,4]Triazolo[1,5-c]Pyrimidine Derivatives 1-gen-2015 FEDERICO, STEPHANIEREDENTI, SARASPALLUTO, GIAMPIERO +
Mixed-reversible and covalent kinase inhibition as a possible new strategy to treat neuro-inflammatory/degenerative diseases 1-gen-2019 Sara RedentiIrene MarcovichRita De ZorziGiampiero SpallutoStephanie Federico +
N8-Isopentyl and N8-Phenylethyl Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine Derivatives as Adenosine Receptor Antagonists 1-gen-2014 FEDERICO, STEPHANIEREDENTI, SARASPALLUTO, GIAMPIERO +
Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidines and Structurally Simplified Analogs. Chemistry and SAR Profile as Adenosine Receptor Antagonists 1-gen-2016 REDENTI, SARAPASTORIN, GIORGIACACCIARI, BarbaraMORO, STEFANOSPALLUTO, GIAMPIEROFEDERICO, STEPHANIE +
Scaffold decoration at positions 5 and 8 of 1,2,4-triazolo[1,5- c ]pyrimidines to explore the antagonist profiling on adenosine receptors: A preliminary structure-activity relationship study 1-gen-2014 FEDERICO, STEPHANIEREDENTI, SARASPALLUTO, GIAMPIERO +
A Triazolotriazine-Based Dual GSK-3β/CK-1δ Ligand as a Potential Neuroprotective Agent Presenting Two Different Mechanisms of Enzymatic Inhibition 1-gen-2019 Redenti, SaraMarcovich, IreneDe Zorzi, RitaSpalluto, GiampieroFederico, Stephanie +