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Journal of Chemical Theory and Computation
|
December 14, 2016
Development of a Simple Electron Transfer and Polarization Model and Its Application to Biological Systems
David J Diller
Current Opinion in Drug Discovery & Development
|
April 23, 2008
The synergy between combinatorial chemistry and high-throughput screening
David J Diller
Journal of Medicinal Chemistry
|
October 17, 2003
Kinases, homology models, and high throughput docking
David J Diller, Rixin Li
Journal of Computer-Aided Molecular Design
|
June 6, 2007
Understanding hERG inhibition with QSAR models based on a one-dimensional molecular representation
David J Diller, Doug W Hobbs
Journal of Chemical Information and Modeling
|
November 26, 2014
VSViewer3D: a tool for interactive data mining of three-dimensional virtual screening data
Kyle I Diller, David J Diller
Journal of Medicinal Chemistry
|
November 30, 2004
Deriving knowledge through data mining high-throughput screening data
David J Diller, Doug W Hobbs
Journal of Computer-Aided Molecular Design
|
August 22, 2002
Can we separate active from inactive conformations?
David J Diller, Kenneth M Merz
Journal of Chemical Information and Modeling
|
June 28, 2007
Library fingerprints: a novel approach to the screening of virtual libraries
Anthony E Klon, David J Diller
Current Topics in Medicinal Chemistry
|
September 24, 2005
The discovery of novel chemotypes of p38 kinase inhibitors
David J Diller, Tsung H Lin, Axel Metzger
Journal of Medicinal Chemistry
|
October 28, 2005
Fast small molecule similarity searching with multiple alignment profiles of molecules represented in one-dimension
Norman Wang, Robert K DeLisle, David J Diller
Page
of 3
Search research articles
Search
Showing results (1-10 of 28) with videos related to
Sort By:
Page
of 3
Journal of Chemical Theory and Computation
|
December 14, 2016
Development of a Simple Electron Transfer and Polarization Model and Its Application to Biological Systems
David J Diller
Current Opinion in Drug Discovery & Development
|
April 23, 2008
The synergy between combinatorial chemistry and high-throughput screening
David J Diller
Journal of Medicinal Chemistry
|
October 17, 2003
Kinases, homology models, and high throughput docking
David J Diller, Rixin Li
Journal of Computer-Aided Molecular Design
|
June 6, 2007
Understanding hERG inhibition with QSAR models based on a one-dimensional molecular representation
David J Diller, Doug W Hobbs
Journal of Chemical Information and Modeling
|
November 26, 2014
VSViewer3D: a tool for interactive data mining of three-dimensional virtual screening data
Kyle I Diller, David J Diller
Journal of Medicinal Chemistry
|
November 30, 2004
Deriving knowledge through data mining high-throughput screening data
David J Diller, Doug W Hobbs
Journal of Computer-Aided Molecular Design
|
August 22, 2002
Can we separate active from inactive conformations?
David J Diller, Kenneth M Merz
Journal of Chemical Information and Modeling
|
June 28, 2007
Library fingerprints: a novel approach to the screening of virtual libraries
Anthony E Klon, David J Diller
Current Topics in Medicinal Chemistry
|
September 24, 2005
The discovery of novel chemotypes of p38 kinase inhibitors
David J Diller, Tsung H Lin, Axel Metzger
Journal of Medicinal Chemistry
|
October 28, 2005
Fast small molecule similarity searching with multiple alignment profiles of molecules represented in one-dimension
Norman Wang, Robert K DeLisle, David J Diller
Page
of 3