Showing results (41-50 of 62) with videos related to
Sort By:
Pageof 7
Future Medicinal Chemistry|June 5, 2014
Halogen-enriched fragment libraries as chemical probes for harnessing halogen bonding in fragment-based lead discoveryMarkus O Zimmermann, Andreas Lange, Rainer Wilcken, et al.Journal of Chemical Theory and Computation|September 18, 2024
Halogen Bonding on Water─A Drop in the Ocean?Marc U Engelhardt, Markus O Zimmermann, Marcel Dammann, et al.ACS Chemical Biology|June 9, 2016
Harnessing Fluorine-Sulfur Contacts and Multipolar Interactions for the Design of p53 Mutant Y220C Rescue DrugsMatthias R Bauer, Rhiannon N Jones, Matthias G J Baud, et al.European Journal of Medicinal Chemistry|July 2, 2019
Synthesis, in vitro biological evaluation and in silico studies of certain arylnicotinic acids conjugated with aryl (thio)semicarbazides as a novel class of anti-leishmanial agentsWagdy M Eldehna, Hadia Almahli, Tamer M Ibrahim, et al.Journal of Molecular Graphics & Modelling|July 3, 2026
A benchmarking-informed structure-based virtual screening strategy targeting Lm-PTR1: Leveraging the Northern African natural products databaseMohamed Abdelfadil, Moataz A Shaldam, Mostafa M Elbadawi, et al.Drug Design, Development and Therapy|July 8, 2024
Evaluation of a Covalent Library of Diverse Warheads (CovLib) Binding to JNK3, USP7, or p53Theresa Klett, Martin Schwer, Larissa N Ernst, et al.Journal of the American Chemical Society|April 28, 2026
Probing Weak Halogen Bonding in Aqueous SolutionManuel A Herbst, Leyun Wu, Yannik T Woordes, et al.Structure (London, England : 1993)|December 5, 2015
Exploiting Transient Protein States for the Design of Small-Molecule Stabilizers of Mutant p53Andreas C Joerger, Matthias R Bauer, Rainer Wilcken, et al.Proceedings of the National Academy of Sciences of the United States of America|October 5, 2012
Lithocholic acid is an endogenous inhibitor of MDM4 and MDM2Simon M Vogel, Matthias R Bauer, Andreas C Joerger, et al.Journal of Medicinal Chemistry|December 16, 2016
Tri- and Tetrasubstituted Pyridinylimidazoles as Covalent Inhibitors of c-Jun N-Terminal Kinase 3Felix Muth, Ahmed El-Gokha, Francesco Ansideri, et al.Pageof 7