Search research articles
Contact Us
Filters
Showing results (81-90 of 98) with videos related to
Page
of 10
Sort By:
RSC Advances
|
July 14, 2015
Synthesis and biological evaluation of non-glucose glycoconjugated <i>N</i>-hydroyxindole class LDH inhibitors as anticancer agents
Valeria Di Bussolo, Emilia C Calvaresi, Carlotta Granchi, et al.
Journal of Medicinal Chemistry
|
September 25, 2009
Design, synthesis, biological evaluation, and NMR studies of a new series of arylsulfones as selective and potent matrix metalloproteinase-12 inhibitors
Elisa Nuti, Laura Panelli, Francesca Casalini, et al.
Journal of Medicinal Chemistry
|
February 14, 2008
Derivatives of 4-amino-6-hydroxy-2-mercaptopyrimidine as novel, potent, and selective A3 adenosine receptor antagonists
Barbara Cosimelli, Giovanni Greco, Marina Ehlardo, et al.
Journal of Medicinal Chemistry
|
November 11, 2005
Synthesis and 3D QSAR of new pyrazolo[3,4-b]pyridines: potent and selective inhibitors of A1 adenosine receptors
Fabrizio Manetti, Silvia Schenone, Francesco Bondavalli, et al.
Journal of Medicinal Chemistry
|
January 7, 2015
Highly selective salicylketoxime-based estrogen receptor β agonists display antiproliferative activities in a glioma model
Ilaria Paterni, Simone Bertini, Carlotta Granchi, et al.
Journal of Medicinal Chemistry
|
May 14, 2009
Rational design, synthesis, and pharmacological properties of new 1,8-naphthyridin-2(1H)-on-3-carboxamide derivatives as highly selective cannabinoid-2 receptor agonists
Clementina Manera, Giuseppe Saccomanni, Barbara Adinolfi, et al.
Bioorganic & Medicinal Chemistry
|
November 14, 2008
Structure-activity relationship studies of a new series of imidazo[2,1-f]purinones as potent and selective A(3) adenosine receptor antagonists
Pier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, et al.
Chemmedchem
|
March 14, 2008
Substituted pyrazolo[3,4-b]pyridines as potent A1 adenosine antagonists: synthesis, biological evaluation, and development of an A1 bovine receptor model
Tiziano Tuccinardi, Silvia Schenone, Francesco Bondavalli, et al.
European Journal of Medicinal Chemistry
|
April 10, 2012
Rational design, synthesis and anti-proliferative properties of new CB2 selective cannabinoid receptor ligands: an investigation of the 1,8-naphthyridin-2(1H)-one scaffold
Clementina Manera, Giuseppe Saccomanni, Anna Maria Malfitano, et al.
European Journal of Medicinal Chemistry
|
September 28, 2011
N-Hydroxyindole-based inhibitors of lactate dehydrogenase against cancer cell proliferation
Carlotta Granchi, Sarabindu Roy, Alessio De Simone, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 98) with videos related to
Sort By:
Page
of 10
RSC Advances
|
July 14, 2015
Synthesis and biological evaluation of non-glucose glycoconjugated <i>N</i>-hydroyxindole class LDH inhibitors as anticancer agents
Valeria Di Bussolo, Emilia C Calvaresi, Carlotta Granchi, et al.
Journal of Medicinal Chemistry
|
September 25, 2009
Design, synthesis, biological evaluation, and NMR studies of a new series of arylsulfones as selective and potent matrix metalloproteinase-12 inhibitors
Elisa Nuti, Laura Panelli, Francesca Casalini, et al.
Journal of Medicinal Chemistry
|
February 14, 2008
Derivatives of 4-amino-6-hydroxy-2-mercaptopyrimidine as novel, potent, and selective A3 adenosine receptor antagonists
Barbara Cosimelli, Giovanni Greco, Marina Ehlardo, et al.
Journal of Medicinal Chemistry
|
November 11, 2005
Synthesis and 3D QSAR of new pyrazolo[3,4-b]pyridines: potent and selective inhibitors of A1 adenosine receptors
Fabrizio Manetti, Silvia Schenone, Francesco Bondavalli, et al.
Journal of Medicinal Chemistry
|
January 7, 2015
Highly selective salicylketoxime-based estrogen receptor β agonists display antiproliferative activities in a glioma model
Ilaria Paterni, Simone Bertini, Carlotta Granchi, et al.
Journal of Medicinal Chemistry
|
May 14, 2009
Rational design, synthesis, and pharmacological properties of new 1,8-naphthyridin-2(1H)-on-3-carboxamide derivatives as highly selective cannabinoid-2 receptor agonists
Clementina Manera, Giuseppe Saccomanni, Barbara Adinolfi, et al.
Bioorganic & Medicinal Chemistry
|
November 14, 2008
Structure-activity relationship studies of a new series of imidazo[2,1-f]purinones as potent and selective A(3) adenosine receptor antagonists
Pier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, et al.
Chemmedchem
|
March 14, 2008
Substituted pyrazolo[3,4-b]pyridines as potent A1 adenosine antagonists: synthesis, biological evaluation, and development of an A1 bovine receptor model
Tiziano Tuccinardi, Silvia Schenone, Francesco Bondavalli, et al.
European Journal of Medicinal Chemistry
|
April 10, 2012
Rational design, synthesis and anti-proliferative properties of new CB2 selective cannabinoid receptor ligands: an investigation of the 1,8-naphthyridin-2(1H)-one scaffold
Clementina Manera, Giuseppe Saccomanni, Anna Maria Malfitano, et al.
European Journal of Medicinal Chemistry
|
September 28, 2011
N-Hydroxyindole-based inhibitors of lactate dehydrogenase against cancer cell proliferation
Carlotta Granchi, Sarabindu Roy, Alessio De Simone, et al.
Page
of 10