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Bioorganic & Medicinal Chemistry
|
October 7, 2016
Methylene versus carbonyl bridge in the structure of new tubulin polymerization inhibitors with tricyclic A-rings
Iuliana-Monica Moise, Elena Bîcu, Joëlle Dubois, et al.
Journal of Chemical Information and Modeling
|
March 3, 2022
SINAPs: A Software Tool for Analysis and Visualization of Interaction Networks of Molecular Dynamics Simulations
Corentin Bedart, Nicolas Renault, Philippe Chavatte, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
May 6, 2015
Docking study: PPARs interaction with the selected alternative plasticizers to di(2-ethylhexyl) phthalate
Nicolas Kambia, Amaury Farce, Karim Belarbi, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
November 27, 2007
Quantitative structure-activity relationships studies of antioxidant hexahydropyridoindoles and flavonoid derivatives
Anne-Catherine Durand, Amaury Farce, Pascal Carato, et al.
Bioorganic & Medicinal Chemistry
|
April 14, 2016
Studies on phenothiazines: New microtubule-interacting compounds with phenothiazine A-ring as potent antineoplastic agents
Alina Ghinet, Iuliana-Monica Moise, Benoît Rigo, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 27, 2014
Peptide chemistry applied to a new family of phenothiazine-containing inhibitors of human farnesyltransferase
Gina-Mirabela Dumitriu, Alina Ghinet, Elena Bîcu, et al.
European Journal of Medicinal Chemistry
|
October 2, 2010
Synthesis, biological evaluation and docking studies of 4-amino-tetrahydroquinazolino[3,2-e]purine derivatives
Valerie Verones, Nathalie Flouquet, Amaury Farce, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 16, 2015
Phenothiazine-based CaaX competitive inhibitors of human farnesyltransferase bearing a cysteine, methionine, serine or valine moiety as a new family of antitumoral compounds
Gina-Mirabela Dumitriu, Elena Bîcu, Dalila Belei, et al.
Journal of Medicinal Chemistry
|
January 11, 2012
Synthesis and structure-activity relationships of (aryloxy)quinazoline ureas as novel, potent, and selective vascular endothelial growth factor receptor-2 inhibitors
Antonio Garofalo, Amaury Farce, Séverine Ravez, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
January 25, 2005
Docking study of ligands into the colchicine binding site of tubulin
Amaury Farce, Cedric Loge, Sebastien Gallet, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
Bioorganic & Medicinal Chemistry
|
October 7, 2016
Methylene versus carbonyl bridge in the structure of new tubulin polymerization inhibitors with tricyclic A-rings
Iuliana-Monica Moise, Elena Bîcu, Joëlle Dubois, et al.
Journal of Chemical Information and Modeling
|
March 3, 2022
SINAPs: A Software Tool for Analysis and Visualization of Interaction Networks of Molecular Dynamics Simulations
Corentin Bedart, Nicolas Renault, Philippe Chavatte, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
May 6, 2015
Docking study: PPARs interaction with the selected alternative plasticizers to di(2-ethylhexyl) phthalate
Nicolas Kambia, Amaury Farce, Karim Belarbi, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
November 27, 2007
Quantitative structure-activity relationships studies of antioxidant hexahydropyridoindoles and flavonoid derivatives
Anne-Catherine Durand, Amaury Farce, Pascal Carato, et al.
Bioorganic & Medicinal Chemistry
|
April 14, 2016
Studies on phenothiazines: New microtubule-interacting compounds with phenothiazine A-ring as potent antineoplastic agents
Alina Ghinet, Iuliana-Monica Moise, Benoît Rigo, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 27, 2014
Peptide chemistry applied to a new family of phenothiazine-containing inhibitors of human farnesyltransferase
Gina-Mirabela Dumitriu, Alina Ghinet, Elena Bîcu, et al.
European Journal of Medicinal Chemistry
|
October 2, 2010
Synthesis, biological evaluation and docking studies of 4-amino-tetrahydroquinazolino[3,2-e]purine derivatives
Valerie Verones, Nathalie Flouquet, Amaury Farce, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 16, 2015
Phenothiazine-based CaaX competitive inhibitors of human farnesyltransferase bearing a cysteine, methionine, serine or valine moiety as a new family of antitumoral compounds
Gina-Mirabela Dumitriu, Elena Bîcu, Dalila Belei, et al.
Journal of Medicinal Chemistry
|
January 11, 2012
Synthesis and structure-activity relationships of (aryloxy)quinazoline ureas as novel, potent, and selective vascular endothelial growth factor receptor-2 inhibitors
Antonio Garofalo, Amaury Farce, Séverine Ravez, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
January 25, 2005
Docking study of ligands into the colchicine binding site of tubulin
Amaury Farce, Cedric Loge, Sebastien Gallet, et al.
Page
of 8