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Journal of Computer-Aided Molecular Design|August 3, 2016
Docking pose selection by interaction pattern graph similarity: application to the D3R grand challenge 2015Inna Slynko, Franck Da Silva, Guillaume Bret, et al.Journal of Chemical Information and Modeling|February 5, 2014
Application of docking and QM/MM-GBSA rescoring to screen for novel Myt1 kinase inhibitorsKanin Wichapong, Alexander Rohe, Charlott Platzer, et al.Journal of Chemical Information and Modeling|January 1, 2014
Virtual screening of PRK1 inhibitors: ensemble docking, rescoring using binding free energy calculation and QSAR model developmentInna Slynko, Michael Scharfe, Tobias Rumpf, et al.Current Alzheimer Research|June 17, 2016
Drug Development of Small-Molecule Inhibitors of AD-Relevant Kinases as Novel Perspective Multitargeted ApproachV Tell, I Hilbrich, M Holzer, et al.Bioorganic & Medicinal Chemistry Letters|March 22, 2014
Discovery of 4-anilino α-carbolines as novel Brk inhibitorsKazem Ahmed Mahmoud, Martin Krug, Tom Wersig, et al.Plos One|April 26, 2012
Lestaurtinib inhibits histone phosphorylation and androgen-dependent gene expression in prostate cancer cellsJens Köhler, German Erlenkamp, Adrien Eberlin, et al.Chemmedchem|July 30, 2016
Identification of Highly Potent Protein Kinase C-Related Kinase 1 Inhibitors by Virtual Screening, Binding Free Energy Rescoring, and in vitro TestingInna Slynko, Karin Schmidtkunz, Tobias Rumpf, et al.Molecules (Basel, Switzerland)|December 15, 2019
Covalent Inhibition of the Histamine H<sub>3</sub> ReceptorGábor Wágner, Tamara A M Mocking, Albert J Kooistra, et al.Molecular Genetics & Genomic Medicine|January 12, 2021
Vanishing white matter: Eukaryotic initiation factor 2B model and the impact of missense mutationsInna Slynko, Stephanie Nguyen, Eline M C Hamilton, et al.Archiv Der Pharmazie|October 30, 2022
SAR exploration of the non-imidazole histamine H<sub>3</sub> receptor ligand ZEL-H16 reveals potent inverse agonismGábor Wágner, Tamara A M Mocking, Xiaoyuan Ma, et al.Pageof 2