FEDERICO, STEPHANIE

FEDERICO, STEPHANIE  

Dipartimento di Scienze Chimiche e Farmaceutiche  

Settore CHIM/08 - Chimica Farmaceutica  

Docenti di ruolo di IIa fascia  

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Risultati 1 - 20 di 78 (tempo di esecuzione: 0.052 secondi).
Titolo Data di pubblicazione Autori File
"Dual Anta-Inhibitors" of the A(2A) Adenosine Receptor and Casein Kinase CK1delta: Synthesis, Biological Evaluation, and Molecular Modeling Studies 1-gen-2023 Cescon, EGrieco, IFederico, SSpalluto, G +
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-c]pyrimidines as New Potent Human A3 Adenosine Receptor Antagonists. 1-gen-2013 SPALLUTO, GIAMPIEROFEDERICO, STEPHANIEMORO, STEFANO +
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 +
8-(2-Furyl)adenine derivatives as A2A adenosine receptor ligands 1-gen-2013 FEDERICO, STEPHANIESPALLUTO, 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 Tools to Investigate A3 Adenosine Receptors in Cancer Cell Lines 1-gen-2023 Federico S.Persico M.Trevisan L.Da Ros T.Gianferrara T.Prencipe F.Pacor S.Spalluto G. +
A Computational Workflow for the Identification of Novel Fragments Acting as Inhibitors of the Activity of Protein Kinase CK1δ 1-gen-2021 Cescon, EleonoraFederico, StephanieSpalluto, Giampiero +
A facile and novel synthesis of N2-, C6-substituted pyrazolo[3,4- d ]pyrimidine-4 carboxylate derivatives as adenosine receptor antagonists 1-gen-2015 FEDERICO, STEPHANIESPALLUTO, GIAMPIERO +
A novel conjugated agent between dopamine and an A2A adenosine receptor antagonists as a potential anti-Parkinson multitarget approach. 1-gen-2012 SPALLUTO, GIAMPIEROFEDERICO, STEPHANIE +
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 +
A2Aadenosine receptor antagonists as therapeutic candidates: Are they still an interesting challenge? 1-gen-2018 Spalluto, GiampieroFederico, Stephanie +
Adenine derivatives as inhibitors of the casein kinase CK1delta enzyme 1-gen-2024 Cescon, EleonoraFederico, StephanieSpalluto, Giampiero +
Adenosine Receptor Ligands, Probes, and Functional Conjugates: A 20-Year History of Pyrazolo[4,3-e][1,2,4]Triazolo[1,5-c]Pyrimidines (PTP) 1-gen-2023 Prencipe F.Da Ros T.Cescon E.Grieco I.Persico M.Spalluto G.Federico S.
Advances in Computational Techniques to Study GPCR-Ligand Recognition 1-gen-2015 FEDERICO, STEPHANIESPALLUTO, GIAMPIERO +
Anticonvulsivanti 1-gen-2015 SPALLUTO, GIAMPIEROFEDERICO, STEPHANIE