Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Dagmar Stumpfe

Showing results (21-30 of 67) with videos related to

Pageof 7
Sort By:
Molecular Informatics|August 3, 2016
Visualization of Activity Landscapes and Chemogenomics DataYe Hu, Dagmar Stumpfe, Jürgen Bajorath
Chemical Biology & Drug Design|May 2, 2015
Identification of orthologous target pairs with shared active compounds and comparison of organism-specific activity patternsDilyana Dimova, Dagmar Stumpfe, Jürgen Bajorath
Journal of Computer-Aided Molecular Design|May 6, 2020
Advances in exploring activity cliffsDagmar Stumpfe, Huabin Hu, Jürgen Bajorath
F1000Research|October 25, 2017
Towards a systematic assessment of assay interference: Identification of extensively tested compounds with high assay promiscuityErik Gilberg, Dagmar Stumpfe, Jürgen Bajorath
Future Science OA|March 24, 2018
Series of screening compounds with high hit rates for the exploration of multi-target activities and assay interferenceDagmar Stumpfe, Erik Gilberg, Jürgen Bajorath
Methods in Molecular Biology (Clifton, N.J.)|September 15, 2010
Molecular test systems for computational selectivity studies and systematic analysis of compound selectivity profilesDagmar Stumpfe, Eugen Lounkine, Jürgen Bajorath
Future Medicinal Chemistry|March 20, 2019
Second-generation activity cliffs identified on the basis of target set-dependent potency difference criteriaHuabin Hu, Dagmar Stumpfe, Jürgen Bajorath
Future Science OA|January 31, 2018
Computational design of new molecular scaffolds for medicinal chemistry, part II: generalization of analog series-based scaffoldsDilyana Dimova, Dagmar Stumpfe, Jürgen Bajorath
Journal of Chemical Information and Modeling|May 10, 2011
Molecular mechanism-based network-like similarity graphs reveal relationships between different types of receptor ligands and structural changes that determine agonistic, inverse-agonistic, and antagonistic effectsPreeti Iyer, Dagmar Stumpfe, Jürgen Bajorath
Bioorganic & Medicinal Chemistry|July 6, 2019
Introducing a new category of activity cliffs with chemical modifications at multiple sites and rationalizing contributions of individual substitutionsDagmar Stumpfe, Huabin Hu, Jürgen Bajorath
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
Molecular Informatics|August 3, 2016
Visualization of Activity Landscapes and Chemogenomics DataYe Hu, Dagmar Stumpfe, Jürgen Bajorath
Chemical Biology & Drug Design|May 2, 2015
Identification of orthologous target pairs with shared active compounds and comparison of organism-specific activity patternsDilyana Dimova, Dagmar Stumpfe, Jürgen Bajorath
Journal of Computer-Aided Molecular Design|May 6, 2020
Advances in exploring activity cliffsDagmar Stumpfe, Huabin Hu, Jürgen Bajorath
F1000Research|October 25, 2017
Towards a systematic assessment of assay interference: Identification of extensively tested compounds with high assay promiscuityErik Gilberg, Dagmar Stumpfe, Jürgen Bajorath
Future Science OA|March 24, 2018
Series of screening compounds with high hit rates for the exploration of multi-target activities and assay interferenceDagmar Stumpfe, Erik Gilberg, Jürgen Bajorath
Methods in Molecular Biology (Clifton, N.J.)|September 15, 2010
Molecular test systems for computational selectivity studies and systematic analysis of compound selectivity profilesDagmar Stumpfe, Eugen Lounkine, Jürgen Bajorath
Future Medicinal Chemistry|March 20, 2019
Second-generation activity cliffs identified on the basis of target set-dependent potency difference criteriaHuabin Hu, Dagmar Stumpfe, Jürgen Bajorath
Future Science OA|January 31, 2018
Computational design of new molecular scaffolds for medicinal chemistry, part II: generalization of analog series-based scaffoldsDilyana Dimova, Dagmar Stumpfe, Jürgen Bajorath
Journal of Chemical Information and Modeling|May 10, 2011
Molecular mechanism-based network-like similarity graphs reveal relationships between different types of receptor ligands and structural changes that determine agonistic, inverse-agonistic, and antagonistic effectsPreeti Iyer, Dagmar Stumpfe, Jürgen Bajorath
Bioorganic & Medicinal Chemistry|July 6, 2019
Introducing a new category of activity cliffs with chemical modifications at multiple sites and rationalizing contributions of individual substitutionsDagmar Stumpfe, Huabin Hu, Jürgen Bajorath
Pageof 7