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PubPharm (14)
1
In vivo phenotypic screening for treating chronic neuropathic pain : modification of C2-arylethynyl group of conformationally constrained A3 adenosine receptor agonists
enthalten in:
Journal of medicinal chemistry
| 2014
von
Tosh, D.
|
Finley, A.
|
Paoletta, S.
| +6
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2
Rational design of sulfonated A3 adenosine receptor-selective nucleosides as pharmacological tools to study chronic neuropathic pain
enthalten in:
Journal of medicinal chemistry
| 2013
von
Paoletta, S.
|
Tosh, D.
|
Finley, A.
| +6
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3
Rational Design of Sulfonated A3 Adenosine Receptor-Selective Nucleosides as Pharmacological Tools To Study Chronic Neuropathic Pain
enthalten in:
Journal of medicinal chemistry
| 2013
von
Paoletta, S.
|
Tosh, D.
|
Finley, A.
| +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 a(3) adenosine receptor antagonists
enthalten in:
Journal of medicinal chemistry
| 2012
von
Federico, S.
|
Ciancetta, A.
|
Sabbadin, D.
| +6
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5
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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6
Structural sweet spot for A1 adenosine receptor activation by truncated (N)-methanocarba nucleosides : receptor docking and potent anticonvulsant activity
enthalten in:
Journal of medicinal chemistry
| 2012
von
Tosh, D.
|
Paoletta, S.
|
Deflorian, F.
| +5
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7
Structural Sweet Spot for A1 Adenosine Receptor Activation by Truncated (N)-Methanocarba Nucleosides: Receptor Docking and Potent Anticonvulsant Activity
enthalten in:
Journal of medicinal chemistry
| 2012
von
Tosh, D.
|
Paoletta, S.
|
Deflorian, F.
| +5
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8
The identification of the 2-phenylphthalazin-1(2H)-one scaffold as a new decorable core skeleton for the design of potent and selective human A3 adenosine receptor antagonists
enthalten in:
Journal of medicinal chemistry
| 2011
von
Poli, D.
|
Catarzi, D.
|
Colotta, V.
| +7
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9
The Identification of the 2-Phenylphthalazin-1(2H)-one Scaffold as a New Decorable Core Skeleton for the Design of Potent and Selective Human A3 Adenosine Receptor Antagonists
enthalten in:
Journal of medicinal chemistry
| 2011
von
Poli, D.
|
Catarzi, D.
|
Colotta, V.
| +7
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10
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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Zeitschrift: Journal of medicinal chemistry
Medienart
14
Aufsätze
8
E-Artikel
8
E-Ressourcen
6
Gedruckte Aufsätze
Zeitschriftentitel
Journal of medicinal chemistry
Thema
8
Journal Article
5
Research Support, Non-U.S. Gov't
4
Receptor, Adenosine A3
4
Research Support, N.I.H., Intramural
3
Adenosine A2 Receptor Antagonists
3
Adenosine A3 Receptor Antagonists
3
Pyrimidines
3
Research Support, N.I.H., Extramural
3
Triazoles
2
Adenosine A3 Receptor Agonists
2
Adenylyl Cyclases
2
EC 4.6.1.1
2
Nucleosides
2
Pyrazoles
2
Triazines
1
059QF0KO0R
1
Acetamides
1
Adenosine A1 Receptor Antagonists
1
Anticonvulsants
1
Furans
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
13
2010-2019
1
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
8
Englisch
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