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Dagmar Stumpfe

Showing results (41-50 of 67) with videos related to

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Future Medicinal Chemistry|February 17, 2015
Structural diversity and potency range distribution of scaffolds from compounds active against current pharmaceutical targetsShilva Kayastha, Dilyana Dimova, Dagmar Stumpfe, et al.
Expert Opinion on Drug Discovery|February 27, 2015
Activity cliff clusters as a source of structure-activity relationship informationDilyana Dimova, Dagmar Stumpfe, Ye Hu, et al.
Journal of Medicinal Chemistry|October 25, 2013
Molecular similarity in medicinal chemistryGerald Maggiora, Martin Vogt, Dagmar Stumpfe, et al.
Journal of Chemical Information and Modeling|April 16, 2013
Compound pathway model to capture SAR progression: comparison of activity cliff-dependent and -independent pathwaysDagmar Stumpfe, Dilyana Dimova, Kathrin Heikamp, et al.
Molecular Pharmaceutics|November 5, 2020
Systematic Data Analysis and Diagnostic Machine Learning Reveal Differences between Compounds with Single- and Multitarget ActivityChristian Feldmann, Dimitar Yonchev, Dagmar Stumpfe, et al.
Journal of Computer-Aided Molecular Design|March 7, 2016
Lessons learned from the design of chemical space networks and opportunities for new applicationsMartin Vogt, Dagmar Stumpfe, Gerald M Maggiora, et al.
Journal of Chemical Information and Modeling|April 12, 2012
MMP-Cliffs: systematic identification of activity cliffs on the basis of matched molecular pairsXiaoying Hu, Ye Hu, Martin Vogt, et al.
Journal of Chemical Information and Modeling|September 30, 2011
Development of a method to consistently quantify the structural distance between scaffolds and to assess scaffold hopping potentialRuifang Li, Dagmar Stumpfe, Martin Vogt, et al.
Journal of Medicinal Chemistry|November 5, 2016
Highly Promiscuous Small Molecules from Biological Screening Assays Include Many Pan-Assay Interference Compounds but Also Candidates for PolypharmacologyErik Gilberg, Swarit Jasial, Dagmar Stumpfe, et al.
Drug Discovery Today|March 22, 2018
Redundancy in two major compound databasesDimitar Yonchev, Dilyana Dimova, Dagmar Stumpfe, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
Future Medicinal Chemistry|February 17, 2015
Structural diversity and potency range distribution of scaffolds from compounds active against current pharmaceutical targetsShilva Kayastha, Dilyana Dimova, Dagmar Stumpfe, et al.
Expert Opinion on Drug Discovery|February 27, 2015
Activity cliff clusters as a source of structure-activity relationship informationDilyana Dimova, Dagmar Stumpfe, Ye Hu, et al.
Journal of Medicinal Chemistry|October 25, 2013
Molecular similarity in medicinal chemistryGerald Maggiora, Martin Vogt, Dagmar Stumpfe, et al.
Journal of Chemical Information and Modeling|April 16, 2013
Compound pathway model to capture SAR progression: comparison of activity cliff-dependent and -independent pathwaysDagmar Stumpfe, Dilyana Dimova, Kathrin Heikamp, et al.
Molecular Pharmaceutics|November 5, 2020
Systematic Data Analysis and Diagnostic Machine Learning Reveal Differences between Compounds with Single- and Multitarget ActivityChristian Feldmann, Dimitar Yonchev, Dagmar Stumpfe, et al.
Journal of Computer-Aided Molecular Design|March 7, 2016
Lessons learned from the design of chemical space networks and opportunities for new applicationsMartin Vogt, Dagmar Stumpfe, Gerald M Maggiora, et al.
Journal of Chemical Information and Modeling|April 12, 2012
MMP-Cliffs: systematic identification of activity cliffs on the basis of matched molecular pairsXiaoying Hu, Ye Hu, Martin Vogt, et al.
Journal of Chemical Information and Modeling|September 30, 2011
Development of a method to consistently quantify the structural distance between scaffolds and to assess scaffold hopping potentialRuifang Li, Dagmar Stumpfe, Martin Vogt, et al.
Journal of Medicinal Chemistry|November 5, 2016
Highly Promiscuous Small Molecules from Biological Screening Assays Include Many Pan-Assay Interference Compounds but Also Candidates for PolypharmacologyErik Gilberg, Swarit Jasial, Dagmar Stumpfe, et al.
Drug Discovery Today|March 22, 2018
Redundancy in two major compound databasesDimitar Yonchev, Dilyana Dimova, Dagmar Stumpfe, et al.
Pageof 7