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Nicolas Saettel

Showing results (1-10 of 14) with videos related to

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Journal of Cheminformatics|November 3, 2016
Benchmark of four popular virtual screening programs: construction of the active/decoy dataset remains a major determinant of measured performanceLudovic Chaput, Juan Martinez-Sanz, Nicolas Saettel, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 26, 2009
Macrocyclic DNA-mismatch-binding ligands: structural determinants of selectivityAnton Granzhan, Eric Largy, Nicolas Saettel, et al.
Current Pharmaceutical Design|March 2, 2012
Screening of a chemical library by HT-G4-FID for discovery of selective G-quadruplex bindersEric Largy, Nicolas Saettel, Florian Hamon, et al.
Journal of Cheminformatics|January 26, 2016
vSDC: a method to improve early recognition in virtual screening when limited experimental resources are availableLudovic Chaput, Juan Martinez-Sanz, Eric Quiniou, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|September 30, 2008
3D Pharmacophore, hierarchical methods, and 5-HT4 receptor binding dataThibault Varin, Nicolas Saettel, Jonathan Villain, et al.
Journal of Nucleic Acids|August 21, 2010
"One Ring to Bind Them All"-Part II: Identification of Promising G-Quadruplex Ligands by Screening of Cyclophane-Type MacrocyclesAnton Granzhan, David Monchaud, Nicolas Saettel, et al.
Journal of Nucleic Acids|August 21, 2010
"One ring to bind them all"-part I: the efficiency of the macrocyclic scaffold for g-quadruplex DNA recognitionDavid Monchaud, Anton Granzhan, Nicolas Saettel, et al.
European Journal of Medicinal Chemistry|November 19, 2013
New aminopyrimidine derivatives as inhibitors of the TAM familyTénin Traoré, Andrea Cavagnino, Nicolas Saettel, et al.
Chemmedchem|March 28, 2007
G-quadruplex recognition by quinacridines: a SAR, NMR, and biological studyCandide Hounsou, Lionel Guittat, David Monchaud, et al.
European Journal of Medicinal Chemistry|July 4, 2012
Inhibitors of the TAM subfamily of tyrosine kinases: synthesis and biological evaluationRosa M Suárez, Franciane Chevot, Andrea Cavagnino, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Journal of Cheminformatics|November 3, 2016
Benchmark of four popular virtual screening programs: construction of the active/decoy dataset remains a major determinant of measured performanceLudovic Chaput, Juan Martinez-Sanz, Nicolas Saettel, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 26, 2009
Macrocyclic DNA-mismatch-binding ligands: structural determinants of selectivityAnton Granzhan, Eric Largy, Nicolas Saettel, et al.
Current Pharmaceutical Design|March 2, 2012
Screening of a chemical library by HT-G4-FID for discovery of selective G-quadruplex bindersEric Largy, Nicolas Saettel, Florian Hamon, et al.
Journal of Cheminformatics|January 26, 2016
vSDC: a method to improve early recognition in virtual screening when limited experimental resources are availableLudovic Chaput, Juan Martinez-Sanz, Eric Quiniou, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|September 30, 2008
3D Pharmacophore, hierarchical methods, and 5-HT4 receptor binding dataThibault Varin, Nicolas Saettel, Jonathan Villain, et al.
Journal of Nucleic Acids|August 21, 2010
"One Ring to Bind Them All"-Part II: Identification of Promising G-Quadruplex Ligands by Screening of Cyclophane-Type MacrocyclesAnton Granzhan, David Monchaud, Nicolas Saettel, et al.
Journal of Nucleic Acids|August 21, 2010
"One ring to bind them all"-part I: the efficiency of the macrocyclic scaffold for g-quadruplex DNA recognitionDavid Monchaud, Anton Granzhan, Nicolas Saettel, et al.
European Journal of Medicinal Chemistry|November 19, 2013
New aminopyrimidine derivatives as inhibitors of the TAM familyTénin Traoré, Andrea Cavagnino, Nicolas Saettel, et al.
Chemmedchem|March 28, 2007
G-quadruplex recognition by quinacridines: a SAR, NMR, and biological studyCandide Hounsou, Lionel Guittat, David Monchaud, et al.
European Journal of Medicinal Chemistry|July 4, 2012
Inhibitors of the TAM subfamily of tyrosine kinases: synthesis and biological evaluationRosa M Suárez, Franciane Chevot, Andrea Cavagnino, et al.
Pageof 2