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Chemistry (Weinheim an Der Bergstrasse, Germany)|January 27, 2025
Discovery of 1,3,4-Oxadiazin-5-One Derivative CJ1-34 as a Partial ATP Synthase Inhibitor for CNS ApplicationsCaitlin V M L Jie, Aro Delparente, Lisa Reichert, et al.Journal of Medicinal Chemistry|February 24, 2011
A class of 5-benzylidene-2-phenylthiazolinones with high potency as direct 5-lipoxygenase inhibitorsBettina Hofmann, Sebastian Barzen, Carmen B Rödl, et al.Nature Reviews. Drug Discovery|April 25, 2015
Predicting drug metabolism: experiment and/or computation?Johannes Kirchmair, Andreas H Göller, Dieter Lang, et al.Bioorganic & Medicinal Chemistry|September 24, 2009
2,4-Diaminopyrimidines as histamine H4 receptor ligands--Scaffold optimization and pharmacological characterizationKerstin Sander, Tim Kottke, Yusuf Tanrikulu, et al.Biological Chemistry|November 5, 2011
Dimerization of human 5-lipoxygenaseAnn-Kathrin Häfner, Mihaela Cernescu, Bettina Hofmann, et al.Analytical Chemistry|March 22, 2018
Binding Specificities of Nanobody•Membrane Protein Complexes Obtained from Chemical Cross-Linking and High-Mass MALDI Mass SpectrometryMartin Köhler, Christoph Neff, Camilo Perez, et al.Bioorganic & Medicinal Chemistry|May 3, 2015
Fragmentation of GW4064 led to a highly potent partial farnesoid X receptor agonist with improved drug-like propertiesDaniel Flesch, Matthias Gabler, Andreas Lill, et al.Plos Computational Biology|June 12, 2013
Scrutinizing MHC-I binding peptides and their limits of variationChristian P Koch, Anna M Perna, Max Pillong, et al.Biochemical Pharmacology|October 20, 2007
Identification and functional analysis of cyclooxygenase-1 as a molecular target of boswellic acidsUlf Siemoneit, Bettina Hofmann, Nicole Kather, et al.Bioorganic & Medicinal Chemistry|November 5, 2013
Synthesis and pharmacological characterization of benzenesulfonamides as dual species inhibitors of human and murine mPGES-1Thomas Hanke, Florian Rörsch, Theresa M Thieme, et al.Pageof 34