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Dora M Schnur

Showing results (1-10 of 9) with videos related to

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Current Opinion in Drug Discovery & Development|April 23, 2008
Recent trends in library design: 'rational design' revisitedDora M Schnur
Methods in Molecular Biology (Clifton, N.J.)|September 15, 2010
Beyond rhodopsin: G protein-coupled receptor structure and modeling incorporating the beta2-adrenergic and adenosine A(2A) crystal structuresAndrew J Tebben, Dora M Schnur
Journal of Medicinal Chemistry|March 17, 2006
Are target-family-privileged substructures truly privileged?Dora M Schnur, Mark A Hermsmeier, Andrew J Tebben
Methods in Molecular Biology (Clifton, N.J.)|September 15, 2010
Methods for combinatorial and parallel library designDora M Schnur, Brett R Beno, Andrew J Tebben, et al.
Steroids|April 10, 2004
Characterization of a new class of selective nonsteroidal progesterone receptor agonistsYu Dong, Jacques Y Roberge, Zhaoqing Wang, et al.
Journal of Combinatorial Chemistry|December 18, 2008
Design and synthesis of a G-protein-coupled receptor antagonist library of aryloxyalkanolamines using a polymer-supported acyclic acetal linkerJacques Y Roberge, Lalgudi S Harikrishnan, Muthoni G Kamau, et al.
Journal of Medicinal Chemistry|February 2, 2013
Discovery of 2-(phenoxypyridine)-3-phenylureas as small molecule P2Y1 antagonistsHannguang Chao, Huji Turdi, Timothy F Herpin, et al.
Journal of Medicinal Chemistry|October 30, 2013
Conformationally constrained ortho-anilino diaryl ureas: discovery of 1-(2-(1'-neopentylspiro[indoline-3,4'-piperidine]-1-yl)phenyl)-3-(4-(trifluoromethoxy)phenyl)urea, a potent, selective, and bioavailable P2Y1 antagonistJennifer X Qiao, Tammy C Wang, Réjean Ruel, et al.
Journal of Medicinal Chemistry|January 24, 2017
Discovery of Pyrrolidine-Containing GPR40 Agonists: Stereochemistry Effects a Change in Binding ModeElizabeth A Jurica, Ximao Wu, Kristin N Williams, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Current Opinion in Drug Discovery & Development|April 23, 2008
Recent trends in library design: 'rational design' revisitedDora M Schnur
Methods in Molecular Biology (Clifton, N.J.)|September 15, 2010
Beyond rhodopsin: G protein-coupled receptor structure and modeling incorporating the beta2-adrenergic and adenosine A(2A) crystal structuresAndrew J Tebben, Dora M Schnur
Journal of Medicinal Chemistry|March 17, 2006
Are target-family-privileged substructures truly privileged?Dora M Schnur, Mark A Hermsmeier, Andrew J Tebben
Methods in Molecular Biology (Clifton, N.J.)|September 15, 2010
Methods for combinatorial and parallel library designDora M Schnur, Brett R Beno, Andrew J Tebben, et al.
Steroids|April 10, 2004
Characterization of a new class of selective nonsteroidal progesterone receptor agonistsYu Dong, Jacques Y Roberge, Zhaoqing Wang, et al.
Journal of Combinatorial Chemistry|December 18, 2008
Design and synthesis of a G-protein-coupled receptor antagonist library of aryloxyalkanolamines using a polymer-supported acyclic acetal linkerJacques Y Roberge, Lalgudi S Harikrishnan, Muthoni G Kamau, et al.
Journal of Medicinal Chemistry|February 2, 2013
Discovery of 2-(phenoxypyridine)-3-phenylureas as small molecule P2Y1 antagonistsHannguang Chao, Huji Turdi, Timothy F Herpin, et al.
Journal of Medicinal Chemistry|October 30, 2013
Conformationally constrained ortho-anilino diaryl ureas: discovery of 1-(2-(1'-neopentylspiro[indoline-3,4'-piperidine]-1-yl)phenyl)-3-(4-(trifluoromethoxy)phenyl)urea, a potent, selective, and bioavailable P2Y1 antagonistJennifer X Qiao, Tammy C Wang, Réjean Ruel, et al.
Journal of Medicinal Chemistry|January 24, 2017
Discovery of Pyrrolidine-Containing GPR40 Agonists: Stereochemistry Effects a Change in Binding ModeElizabeth A Jurica, Ximao Wu, Kristin N Williams, et al.
Pageof 1