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journalStr:"Journal of medicinal chemistry"
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PubPharm (25)
1
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
enthalten in:
Journal of medicinal chemistry
| 2014
von
Federico, S.
|
Ciancetta, A.
|
Porta, N.
| +6
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2
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
enthalten in:
Journal of medicinal chemistry
| 2014
von
Federico, S.
|
Ciancetta, A.
|
Porta, N.
| +6
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3
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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4
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 A3 Adenosine Receptor Antagonists.
enthalten in:
Journal of medicinal chemistry
| 2012
von
Federico, S.
|
Ciancetta, A.
|
Sabbadin, D.
| +6
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5
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
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6
Synthesis and Biological Evaluation of a New Series of 1,2,4-Triazolo[1,5-a]-1,3,5-triazines as Human A2A Adenosine Receptor Antagonists with Improved Water Solubility
enthalten in:
Journal of medicinal chemistry
| 2011
von
Federico, S.
|
Paoletta, S.
|
Cheong, S.
| +9
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7
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
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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 hA3 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
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9
Synthesis and biological studies of a new series of 5-heteroarylcarbamoylaminopyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidines as human A3 adenosine receptor antagonists. Influence of the heteroaryl substituent on binding affinity and molecular modeling investigations
enthalten in:
Journal of medicinal chemistry
| 2006
von
Pastorin, G.
|
Da Ros, T.
|
Bolcato, C.
| +7
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10
Autocorrelation of molecular electrostatic potential surface properties combined with partial least squares analysis as new strategy for the prediction of the activity of human A(3) adenosine receptor antagonists
enthalten in:
Journal of medicinal chemistry
| 2005
von
Moro, S.
|
Bacilieri, M.
|
Cacciari, B.
| +1
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Zeitschrift: Journal of medicinal chemistry
Medienart
25
Aufsätze
21
Gedruckte Aufsätze
4
E-Artikel
4
E-Ressourcen
Zeitschriftentitel
Journal of medicinal chemistry
Thema
12
Journal Article
11
Research Support, Non-U.S. Gov't
9
Pyrimidines
8
Receptor, Adenosine A3
7
Triazoles
6
Purinergic P1 Receptor Antagonists
4
Adenosine A3 Receptor Antagonists
4
Receptors, Purinergic P1
3
Pyrazoles
2
Adenosine A2 Receptor Antagonists
2
Adenylyl Cyclases
2
Cyclic AMP
2
E0399OZS9N
2
EC 4.6.1.1
2
Furans
2
Ligands
2
Receptor, Adenosine A2A
1
059QF0KO0R
1
1,2,4-triazolo(1,5-c)pyrimidine
1
35920-39-9
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Erscheinungszeitraum
19
2000-
6
1900-1999
Erscheinungsjahr(e)
Von:
Bis:
Sprache
12
Englisch
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