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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
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February 19, 2008
A short series of antidiabetic sulfonylureas exhibit multiple ligand PPARgamma-binding patterns
Alban Arrault, Stéphane Rocchi, Frédéric Picard, et al.
European Journal of Medicinal Chemistry
|
January 21, 2014
N-(3-Arylaminopyridin-4-yl)alkanesulfonamides as pyridine analogs of nimesulide: cyclooxygenases inhibition, anti-inflammatory studies and insight on metabolism
Jean-François Renard, Frédéric Lecomte, Philippe Hubert, et al.
Biochemical Pharmacology
|
September 20, 2015
Forskolin-free cAMP assay for Gi-coupled receptors
Julie Gilissen, Pierre Geubelle, Nadine Dupuis, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 23, 2002
Structural approach of the mechanism of inhibition of alpha-chymotrypsin by coumarins
Johan Wouters, Marjorie Huygens, Lionel Pochet, et al.
Current Medicinal Chemistry
|
April 23, 2002
New trends in dual 5-LOX/COX inhibition
Xavier de Leval, Fabien Julemont, Jacques Delarge, et al.
International Immunopharmacology
|
October 9, 2008
Coumarinic derivatives show anti-inflammatory effects on alveolar macrophages, but their anti-elastase activity is essential to reduce lung inflammation in vivo
Elyse Y Bissonnette, Guy M Tremblay, Véronique Turmel, et al.
Recent Patents on CNS Drug Discovery
|
January 29, 2008
In search of novel AMPA potentiators
Pierre Francotte, Pascal de Tullio, Pierre Fraikin, et al.
Journal of Medicinal Chemistry
|
July 21, 2006
Design, synthesis, and pharmacological evaluation of R/S-3,4-dihydro-2,2-dimethyl- 6-halo-4-(phenylaminocarbonylamino)-2H-1-benzopyrans: toward tissue-selective pancreatic beta-cell KATP channel openers structurally related to (+/-)-cromakalim
Sophie Sebille, David Gall, Pascal de Tullio, et al.
Journal of Medicinal Chemistry
|
December 13, 2006
Three-dimensional quantitative structure-activity relationships of ATP-sensitive potassium (KATP) channel openers belonging to the 3-alkylamino-4H-1,2,4-benzo- and 3-alkylamino-4H-1,2,4-pyridothiadiazine 1,1-dioxide families
Pascal de Tullio, Léon Dupont, Pierre Francotte, et al.
European Journal of Medicinal Chemistry
|
April 26, 2014
Influence of the alkylsulfonylamino substituent located at the 6-position of 2,2-dimethylchromans structurally related to cromakalim: from potassium channel openers to calcium entry blockers?
Xavier Florence, Vincent Desvaux, Eric Goffin, et al.
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of 13
Search research articles
Search
Showing results (21-30 of 124) with videos related to
Sort By:
Page
of 13
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
February 19, 2008
A short series of antidiabetic sulfonylureas exhibit multiple ligand PPARgamma-binding patterns
Alban Arrault, Stéphane Rocchi, Frédéric Picard, et al.
European Journal of Medicinal Chemistry
|
January 21, 2014
N-(3-Arylaminopyridin-4-yl)alkanesulfonamides as pyridine analogs of nimesulide: cyclooxygenases inhibition, anti-inflammatory studies and insight on metabolism
Jean-François Renard, Frédéric Lecomte, Philippe Hubert, et al.
Biochemical Pharmacology
|
September 20, 2015
Forskolin-free cAMP assay for Gi-coupled receptors
Julie Gilissen, Pierre Geubelle, Nadine Dupuis, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 23, 2002
Structural approach of the mechanism of inhibition of alpha-chymotrypsin by coumarins
Johan Wouters, Marjorie Huygens, Lionel Pochet, et al.
Current Medicinal Chemistry
|
April 23, 2002
New trends in dual 5-LOX/COX inhibition
Xavier de Leval, Fabien Julemont, Jacques Delarge, et al.
International Immunopharmacology
|
October 9, 2008
Coumarinic derivatives show anti-inflammatory effects on alveolar macrophages, but their anti-elastase activity is essential to reduce lung inflammation in vivo
Elyse Y Bissonnette, Guy M Tremblay, Véronique Turmel, et al.
Recent Patents on CNS Drug Discovery
|
January 29, 2008
In search of novel AMPA potentiators
Pierre Francotte, Pascal de Tullio, Pierre Fraikin, et al.
Journal of Medicinal Chemistry
|
July 21, 2006
Design, synthesis, and pharmacological evaluation of R/S-3,4-dihydro-2,2-dimethyl- 6-halo-4-(phenylaminocarbonylamino)-2H-1-benzopyrans: toward tissue-selective pancreatic beta-cell KATP channel openers structurally related to (+/-)-cromakalim
Sophie Sebille, David Gall, Pascal de Tullio, et al.
Journal of Medicinal Chemistry
|
December 13, 2006
Three-dimensional quantitative structure-activity relationships of ATP-sensitive potassium (KATP) channel openers belonging to the 3-alkylamino-4H-1,2,4-benzo- and 3-alkylamino-4H-1,2,4-pyridothiadiazine 1,1-dioxide families
Pascal de Tullio, Léon Dupont, Pierre Francotte, et al.
European Journal of Medicinal Chemistry
|
April 26, 2014
Influence of the alkylsulfonylamino substituent located at the 6-position of 2,2-dimethylchromans structurally related to cromakalim: from potassium channel openers to calcium entry blockers?
Xavier Florence, Vincent Desvaux, Eric Goffin, et al.
Page
of 13