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PubPharm (105)
41
Discovery of simplified N²-substituted pyrazolo[3,4-d]pyrimidine derivatives as novel adenosine receptor antagonists : efficient synthetic approaches, biological evaluations and molecular docking studies
enthalten in:
Bioorganic & medicinal chemistry
| 2014
von
Venkatesan, G.
|
Paira, P.
|
Cheong, S.
| +5
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42
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
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43
The A3 adenosine receptor as multifaceted therapeutic target : pharmacology, medicinal chemistry, and in silico approaches
enthalten in:
Medicinal research reviews
| 2013
von
Cheong, S.
|
Federico, S.
|
Venkatesan, G.
| +5
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44
8-(2-Furyl)adenine derivatives as A₂A adenosine receptor ligands
enthalten in:
European journal of medicinal chemistry
| 2013
von
Dal Ben, D.
|
Buccioni, M.
|
Lambertucci, C.
| +6
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45
Fluorescent ligands for adenosine receptors
enthalten in:
Bioorganic & medicinal chemistry letters
| 2013
von
Kozma, E.
|
Jayasekara, P.
|
Squarcialupi, L.
| +5
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46
Exploring the directionality of 5-substitutions in a new series of 5-alkylaminopyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine as a strategy to design novel human a(3) adenosine receptor antagonists
enthalten in:
Journal of medicinal chemistry
| 2012
von
Federico, S.
|
Ciancetta, A.
|
Sabbadin, D.
| +6
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47
Novel fluorescent antagonist as a molecular probe in A(3) adenosine receptor binding assays using flow cytometry
enthalten in:
Biochemical pharmacology
| 2012
von
Kozma, E.
|
Kumar, T.
|
Federico, S.
| +7
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48
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.
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49
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
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50
Does the combination of optimal substitutions at the C²-, N⁵- and N⁸-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A₃ adenosine receptors?
enthalten in:
Bioorganic & medicinal chemistry
| 2011
von
Cheong, S.
|
Dolzhenko, A.
|
Paoletta, S.
| +8
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Sprache: Englisch
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Journal of medicinal chemistry
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Purinergic signalling
7
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Thema
84
Journal Article
46
Research Support, Non-U.S. Gov't
25
Pyrimidines
24
Receptor, Adenosine A3
24
Triazoles
23
Review
22
Purinergic P1 Receptor Antagonists
16
Ligands
15
Adenosine A3 Receptor Antagonists
14
Adenosine A2 Receptor Antagonists
14
Receptors, Purinergic P1
13
Pyrazoles
11
Receptor, Adenosine A2A
9
Adenosine receptors
7
Molecular modeling
6
Receptors, G-Protein-Coupled
6
Triazines
5
Adenine derivatives
5
EC 2.7.11.1
5
GPCR
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Erscheinungszeitraum
95
2000-
2
1900-1999
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