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March 5, 2003
Computational approaches towards the quantification of molecular diversity and design of compound libraries
Hans Matter
Journal of Medicinal Chemistry
|
May 31, 2002
Structural classification of protein kinases using 3D molecular interaction field analysis of their ligand binding sites: target family landscapes
Thorsten Naumann, Hans Matter
Medicinal Research Reviews
|
June 30, 2004
Biology and chemistry of the inhibition of nitric oxide synthases by pteridine-derivatives as therapeutic agents
Hans Matter, Peter Kotsonis
Bioorganic & Medicinal Chemistry Letters
|
June 9, 2018
Characterizing hydration sites in protein-ligand complexes towards the design of novel ligands
Hans Matter, Stefan Güssregen
Journal of Medicinal Chemistry
|
January 6, 2006
Matrix metalloproteinase target family landscape: a chemometrical approach to ligand selectivity based on protein binding site analysis
Bernard Pirard, Hans Matter
Current Opinion in Drug Discovery & Development
|
September 2, 2004
Recent advances in the design of matrix metalloprotease inhibitors
Hans Matter, Manfred Schudok
Current Opinion in Chemical Biology
|
August 4, 2004
Integrating virtual screening in lead discovery
Tudor I Oprea, Hans Matter
Methods in Molecular Biology (Clifton, N.J.)
|
November 3, 2021
Artificial Intelligence in Compound Design
Christoph Grebner, Hans Matter, Gerhard Hessler
Journal of Chemical Information and Modeling
|
January 8, 2019
Predictive Multitask Deep Neural Network Models for ADME-Tox Properties: Learning from Large Data Sets
Jan Wenzel, Hans Matter, Friedemann Schmidt
Journal of Medicinal Chemistry
|
August 19, 2005
Virtual screening of biogenic amine-binding G-protein coupled receptors: comparative evaluation of protein- and ligand-based virtual screening protocols
Andreas Evers, Gerhard Hessler, Hans Matter, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 66) with videos related to
Sort By:
Page
of 7
EXS
|
March 5, 2003
Computational approaches towards the quantification of molecular diversity and design of compound libraries
Hans Matter
Journal of Medicinal Chemistry
|
May 31, 2002
Structural classification of protein kinases using 3D molecular interaction field analysis of their ligand binding sites: target family landscapes
Thorsten Naumann, Hans Matter
Medicinal Research Reviews
|
June 30, 2004
Biology and chemistry of the inhibition of nitric oxide synthases by pteridine-derivatives as therapeutic agents
Hans Matter, Peter Kotsonis
Bioorganic & Medicinal Chemistry Letters
|
June 9, 2018
Characterizing hydration sites in protein-ligand complexes towards the design of novel ligands
Hans Matter, Stefan Güssregen
Journal of Medicinal Chemistry
|
January 6, 2006
Matrix metalloproteinase target family landscape: a chemometrical approach to ligand selectivity based on protein binding site analysis
Bernard Pirard, Hans Matter
Current Opinion in Drug Discovery & Development
|
September 2, 2004
Recent advances in the design of matrix metalloprotease inhibitors
Hans Matter, Manfred Schudok
Current Opinion in Chemical Biology
|
August 4, 2004
Integrating virtual screening in lead discovery
Tudor I Oprea, Hans Matter
Methods in Molecular Biology (Clifton, N.J.)
|
November 3, 2021
Artificial Intelligence in Compound Design
Christoph Grebner, Hans Matter, Gerhard Hessler
Journal of Chemical Information and Modeling
|
January 8, 2019
Predictive Multitask Deep Neural Network Models for ADME-Tox Properties: Learning from Large Data Sets
Jan Wenzel, Hans Matter, Friedemann Schmidt
Journal of Medicinal Chemistry
|
August 19, 2005
Virtual screening of biogenic amine-binding G-protein coupled receptors: comparative evaluation of protein- and ligand-based virtual screening protocols
Andreas Evers, Gerhard Hessler, Hans Matter, et al.
Page
of 7