Suchergebnisse - (Person:"Federico, Stephanie")

PubPharm (10)

1

Design, Synthesis and Evaluation of New Indolylpyrimidylpiperazines for Gastrointestinal Cancer Therapy

enthalten in: Molecules (Basel, Switzerland) | 2019

von Tan, A. | Babak, M. | Venkatesan, G. | +10

2

A2A Adenosine Receptor Antagonists as Therapeutic Candidates : Are They Still an Interesting Challenge?

enthalten in: Mini reviews in medicinal chemistry | 2018

von Cacciari, B. | Spalluto, G. | Federico, S.

3

Discovery of indolylpiperazinylpyrimidines with dual-target profiles at adenosine A2A and dopamine D2 receptors for Parkinson's disease treatment

enthalten in: PloS one | 2018

von Shao, Y. | Ma, X. | Paira, P. | +11

4

Revisiting a receptor-based pharmacophore hypothesis for human A(2A) adenosine receptor antagonists

enthalten in: Journal of chemical information and modeling | 2013

von Bacilieri, M. | Ciancetta, A. | Paoletta, S. | +9

5

Therapeutic potential of A2 and A3 adenosine receptor : a review of novel patented ligands

enthalten in: Expert opinion on therapeutic patents | 2012

von Federico, S. | Spalluto, G.

6

A novel conjugated agent between dopamine and an A2A adenosine receptor antagonist as a potential anti-Parkinson multitarget approach

enthalten in: Molecular pharmaceutics | 2012

von Dalpiaz, A. | Cacciari, B. | Vicentini, C. | +7

7

Synthesis and biological evaluation of a new series of 1,2,4-triazolo[1,5-a]-1,3,5-triazines as human A(2A) adenosine receptor antagonists with improved water solubility

enthalten in: Journal of medicinal chemistry | 2011

von Federico, S. | Paoletta, S. | Cheong, S. | +9

8

The significance of 2-furyl ring substitution with a 2-(para-substituted) aryl group in a new series of pyrazolo-triazolo-pyrimidines as potent and highly selective hA(3) adenosine receptors antagonists : new insights into structure-affinity relationship and receptor-antagonist recognition

enthalten in: Journal of medicinal chemistry | 2010

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

9

Synthesis and pharmacological characterization of a new series of 5,7-disubstituted-[1,2,4]triazolo[1,5-a][1,3,5]triazine derivatives as adenosine receptor antagonists : A preliminary inspection of ligand-receptor recognition process

enthalten in: Bioorganic & medicinal chemistry | 2010

von Pastorin, G. | Federico, S. | Paoletta, S. | +8

10

Combining selectivity and affinity predictions using an integrated Support Vector Machine (SVM) approach : An alternative tool to discriminate between the human adenosine A(2A) and A(3) receptor pyrazolo-triazolo-pyrimidine antagonists binding sites

enthalten in: Bioorganic & medicinal chemistry | 2009

von Michielan, L. | Bolcato, C. | Federico, S. | +9

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