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Eric Therrien

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Journal of Medicinal Chemistry|September 29, 2006
A method for induced-fit docking, scoring, and ranking of flexible ligands. Application to peptidic and pseudopeptidic beta-secretase (BACE 1) inhibitorsNicolas Moitessier, Eric Therrien, Stephen Hanessian
Bioorganic & Medicinal Chemistry Letters|May 9, 2015
Design and synthesis of close analogs of LCRF-0004, a potent and selective RON receptor tyrosine kinase inhibitorStéphane L Raeppel, Franck Raeppel, Eric Therrien
Bioorganic & Medicinal Chemistry Letters|August 6, 2015
Design, synthesis and RON receptor tyrosine kinase inhibitory activity of new head groups analogs of LCRF-0004Franck Raeppel, Stéphane L Raeppel, Eric Therrien
Bioorganic & Medicinal Chemistry Letters|June 27, 2015
Design and synthesis of constrained analogs of LCRF-0004 as potent RON tyrosine kinase inhibitorsStéphane L Raeppel, Eric Therrien, Franck Raeppel
Bioorganic & Medicinal Chemistry Letters|September 25, 2002
Targeting thrombin and factor VIIa: design, synthesis, and inhibitory activity of functionally relevant indolizidinonesStephen Hanessian, Eric Therrien, Kenneth Granberg, et al.
The Journal of Organic Chemistry|September 13, 2003
Synthesis of diversely functionalized indolizidinones and related bicyclic lactams using intramolecular Grubbs olefin metathesis and Dieckmann condensationStephen Hanessian, Helen Sailes, Alexander Munro, et al.
Current Pharmaceutical Design|August 17, 2013
Methods for docking small molecules to macromolecules: a user's perspective. 2. ApplicationsValérie Campagna-Slater, Eric Therrien, Nathanael Weill, et al.
Current Pharmaceutical Design|August 17, 2013
Methods for docking small molecules to macromolecules: a user's perspective. 1. The theoryNathanael Weill, Eric Therrien, Valérie Campagna-Slater, et al.
Journal of Chemical Information and Modeling|December 25, 2013
Docking ligands into flexible and solvated macromolecules. 6. Development and application to the docking of HDACs and other zinc metalloenzymes inhibitorsJoshua Pottel, Eric Therrien, James L Gleason, et al.
The Journal of Organic Chemistry|July 17, 2004
Synthesis of 3 10-helix-inducing constrained analogues of L-prolineStephen Hanessian, Gianluca Papeo, Kamal Fettis, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Journal of Medicinal Chemistry|September 29, 2006
A method for induced-fit docking, scoring, and ranking of flexible ligands. Application to peptidic and pseudopeptidic beta-secretase (BACE 1) inhibitorsNicolas Moitessier, Eric Therrien, Stephen Hanessian
Bioorganic & Medicinal Chemistry Letters|May 9, 2015
Design and synthesis of close analogs of LCRF-0004, a potent and selective RON receptor tyrosine kinase inhibitorStéphane L Raeppel, Franck Raeppel, Eric Therrien
Bioorganic & Medicinal Chemistry Letters|August 6, 2015
Design, synthesis and RON receptor tyrosine kinase inhibitory activity of new head groups analogs of LCRF-0004Franck Raeppel, Stéphane L Raeppel, Eric Therrien
Bioorganic & Medicinal Chemistry Letters|June 27, 2015
Design and synthesis of constrained analogs of LCRF-0004 as potent RON tyrosine kinase inhibitorsStéphane L Raeppel, Eric Therrien, Franck Raeppel
Bioorganic & Medicinal Chemistry Letters|September 25, 2002
Targeting thrombin and factor VIIa: design, synthesis, and inhibitory activity of functionally relevant indolizidinonesStephen Hanessian, Eric Therrien, Kenneth Granberg, et al.
The Journal of Organic Chemistry|September 13, 2003
Synthesis of diversely functionalized indolizidinones and related bicyclic lactams using intramolecular Grubbs olefin metathesis and Dieckmann condensationStephen Hanessian, Helen Sailes, Alexander Munro, et al.
Current Pharmaceutical Design|August 17, 2013
Methods for docking small molecules to macromolecules: a user's perspective. 2. ApplicationsValérie Campagna-Slater, Eric Therrien, Nathanael Weill, et al.
Current Pharmaceutical Design|August 17, 2013
Methods for docking small molecules to macromolecules: a user's perspective. 1. The theoryNathanael Weill, Eric Therrien, Valérie Campagna-Slater, et al.
Journal of Chemical Information and Modeling|December 25, 2013
Docking ligands into flexible and solvated macromolecules. 6. Development and application to the docking of HDACs and other zinc metalloenzymes inhibitorsJoshua Pottel, Eric Therrien, James L Gleason, et al.
The Journal of Organic Chemistry|July 17, 2004
Synthesis of 3 10-helix-inducing constrained analogues of L-prolineStephen Hanessian, Gianluca Papeo, Kamal Fettis, et al.
Pageof 3