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Chemmedchem
|
December 25, 2014
The use of thermodynamic and kinetic data in drug discovery: decisive insight or increasing the puzzlement?
Gerhard Klebe
Drug Discovery Today. Technologies
|
July 2, 2014
Lead identification in post-genomics: computers as a complementary alternative
Gerhard Klebe
Nature Reviews. Drug Discovery
|
January 24, 2015
Applying thermodynamic profiling in lead finding and optimization
Gerhard Klebe
Journal of Medicinal Chemistry
|
February 17, 2026
Thermodynamic Data Remain a Hot Tip for Decoding Binding Affinity and Water Impact on Protein-Ligand Complex Formation to Assist Lead Optimization
Gerhard Klebe
Drug Discovery Today
|
February 2, 2019
Broad-scale analysis of thermodynamic signatures in medicinal chemistry: are enthalpy-favored binders the better development option?
Gerhard Klebe
Drug Discovery Today
|
June 24, 2006
Virtual ligand screening: strategies, perspectives and limitations
Gerhard Klebe
Journal of Chemical Information and Modeling
|
August 26, 2011
DSX: a knowledge-based scoring function for the assessment of protein-ligand complexes
Gerd Neudert, Gerhard Klebe
Proteins
|
November 19, 2011
Cofactor-binding sites in proteins of deviating sequence: comparative analysis and clustering in torsion angle, cavity, and fold space
Björn Stegemann, Gerhard Klebe
Journal of Medicinal Chemistry
|
September 6, 2002
DrugScore meets CoMFA: adaptation of fields for molecular comparison (AFMoC) or how to tailor knowledge-based pair-potentials to a particular protein
Holger Gohlke, Gerhard Klebe
Angewandte Chemie (International Ed. in English)
|
August 31, 2002
Approaches to the description and prediction of the binding affinity of small-molecule ligands to macromolecular receptors
Holger Gohlke, Gerhard Klebe
Page
of 27
Search research articles
Search
Showing results (1-10 of 262) with videos related to
Sort By:
Page
of 27
Chemmedchem
|
December 25, 2014
The use of thermodynamic and kinetic data in drug discovery: decisive insight or increasing the puzzlement?
Gerhard Klebe
Drug Discovery Today. Technologies
|
July 2, 2014
Lead identification in post-genomics: computers as a complementary alternative
Gerhard Klebe
Nature Reviews. Drug Discovery
|
January 24, 2015
Applying thermodynamic profiling in lead finding and optimization
Gerhard Klebe
Journal of Medicinal Chemistry
|
February 17, 2026
Thermodynamic Data Remain a Hot Tip for Decoding Binding Affinity and Water Impact on Protein-Ligand Complex Formation to Assist Lead Optimization
Gerhard Klebe
Drug Discovery Today
|
February 2, 2019
Broad-scale analysis of thermodynamic signatures in medicinal chemistry: are enthalpy-favored binders the better development option?
Gerhard Klebe
Drug Discovery Today
|
June 24, 2006
Virtual ligand screening: strategies, perspectives and limitations
Gerhard Klebe
Journal of Chemical Information and Modeling
|
August 26, 2011
DSX: a knowledge-based scoring function for the assessment of protein-ligand complexes
Gerd Neudert, Gerhard Klebe
Proteins
|
November 19, 2011
Cofactor-binding sites in proteins of deviating sequence: comparative analysis and clustering in torsion angle, cavity, and fold space
Björn Stegemann, Gerhard Klebe
Journal of Medicinal Chemistry
|
September 6, 2002
DrugScore meets CoMFA: adaptation of fields for molecular comparison (AFMoC) or how to tailor knowledge-based pair-potentials to a particular protein
Holger Gohlke, Gerhard Klebe
Angewandte Chemie (International Ed. in English)
|
August 31, 2002
Approaches to the description and prediction of the binding affinity of small-molecule ligands to macromolecular receptors
Holger Gohlke, Gerhard Klebe
Page
of 27