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European Journal of Medicinal Chemistry
|
October 17, 2003
New N6- or N(9)-hydroxyalkyl substituted 8-azaadenines or adenines as effective A1 adenosine receptor ligands
Giuliana Biagi, Irene Giorgi, Michele Leonardi, et al.
Bioorganic & Medicinal Chemistry
|
November 26, 2008
QSAR studies on BK channel activators
Alessio Coi, Francesca Lidia Fiamingo, Oreste Livi, et al.
European Journal of Medicinal Chemistry
|
June 9, 2004
Synthesis and biological activity of novel substituted benzanilides as potassium channel activators. V
Giuliana Biagi, Irene Giorgi, Oreste Livi, et al.
European Journal of Medicinal Chemistry
|
October 13, 2006
Structural modifications of benzanilide derivatives, effective potassium channel openers. X
Vincenzo Calderone, Alessio Coi, Francesca Lidia Fiamingo, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
May 7, 2002
Erythro- and threo-2-hydroxynonyl substituted 2-phenyladenines and 2-phenyl-8-azaadenines: ligands for A1 adenosine receptors and adenosine deaminase
Giuliana Biagi, Irene Giorgi, Oreste Livi, et al.
European Journal of Medicinal Chemistry
|
November 30, 2007
N6-1,3-diphenylurea derivatives of 2-phenyl-9-benzyladenines and 8-azaadenines: synthesis and biological evaluation as allosteric modulators of A2A adenosine receptors
Irene Giorgi, Giuliana Biagi, Anna Maria Bianucci, et al.
European Journal of Medicinal Chemistry
|
October 10, 2006
Synthesis, biological activity and molecular modelling of new trisubstituted 8-azaadenines with high affinity for A1 adenosine receptors
Irene Giorgi, Anna Maria Bianucci, Giuliana Biagi, et al.
Bioorganic & Medicinal Chemistry
|
May 24, 2005
2,9-disubstituted-N6-(arylcarbamoyl)-8-azaadenines as new selective A3 adenosine receptor antagonists: synthesis, biochemical and molecular modelling studies
Giuliana Biagi, Anna Maria Bianucci, Alessio Coi, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
European Journal of Medicinal Chemistry
|
October 17, 2003
New N6- or N(9)-hydroxyalkyl substituted 8-azaadenines or adenines as effective A1 adenosine receptor ligands
Giuliana Biagi, Irene Giorgi, Michele Leonardi, et al.
Bioorganic & Medicinal Chemistry
|
November 26, 2008
QSAR studies on BK channel activators
Alessio Coi, Francesca Lidia Fiamingo, Oreste Livi, et al.
European Journal of Medicinal Chemistry
|
June 9, 2004
Synthesis and biological activity of novel substituted benzanilides as potassium channel activators. V
Giuliana Biagi, Irene Giorgi, Oreste Livi, et al.
European Journal of Medicinal Chemistry
|
October 13, 2006
Structural modifications of benzanilide derivatives, effective potassium channel openers. X
Vincenzo Calderone, Alessio Coi, Francesca Lidia Fiamingo, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
May 7, 2002
Erythro- and threo-2-hydroxynonyl substituted 2-phenyladenines and 2-phenyl-8-azaadenines: ligands for A1 adenosine receptors and adenosine deaminase
Giuliana Biagi, Irene Giorgi, Oreste Livi, et al.
European Journal of Medicinal Chemistry
|
November 30, 2007
N6-1,3-diphenylurea derivatives of 2-phenyl-9-benzyladenines and 8-azaadenines: synthesis and biological evaluation as allosteric modulators of A2A adenosine receptors
Irene Giorgi, Giuliana Biagi, Anna Maria Bianucci, et al.
European Journal of Medicinal Chemistry
|
October 10, 2006
Synthesis, biological activity and molecular modelling of new trisubstituted 8-azaadenines with high affinity for A1 adenosine receptors
Irene Giorgi, Anna Maria Bianucci, Giuliana Biagi, et al.
Bioorganic & Medicinal Chemistry
|
May 24, 2005
2,9-disubstituted-N6-(arylcarbamoyl)-8-azaadenines as new selective A3 adenosine receptor antagonists: synthesis, biochemical and molecular modelling studies
Giuliana Biagi, Anna Maria Bianucci, Alessio Coi, et al.
Page
of 2