Sippl, Wolfgang, 1965-
Sippl, Wölfgang
Sippl, Wolfgang 19..-.... professeur
Wolfgang Sippl researcher
VIAF ID: 40165729 (Personal)
Permalink: http://viaf.org/viaf/40165729
Preferred Forms
- 200 _ | ‡a Sippl ‡b Wolfgang ‡f 19..-.... ‡c professeur
- 100 1 _ ‡a Sippl, Wolfgang
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- 100 1 _ ‡a Sippl, Wolfgang ‡d 1965-
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- 100 1 _ ‡a Sippl, Wölfgang
- 100 1 _ ‡a Sippl, Wölfgang
- 100 0 _ ‡a Wolfgang Sippl ‡c researcher
4xx's: Alternate Name Forms (3)
5xx's: Related Names (1)
Works
Title | Sources |
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Anwendung computergestützter Methoden für Interaktionsstudien und Entwicklung Subtyp-selektiver Inhibitoren von Histondeacetylasen | |
Application of computer-based methods to identify and investigate ligands for proteins with high flexible binding sites | |
Carbamates as potential prodrugs and a new<br>warhead for HDAC inhibition | |
cyanobacterium Aetokthonos hydrillicola : more than just an “eagle killer”? | |
Defined stereoisomers of 2″-amino NAD+ and their activity against human sirtuins and a bacterial (ADP-ribosyl) transferase | |
Design and synthesis of antimycobacterial agents targeting the mycobacterial electron transport chain and the cell wall synthesis, and in vitro testing against different mycobacterial species | |
Development of a NanoBRET assay to validate inhibitors of Sirt2-mediated lysine deacetylation and defatty-acylation that block prostate cancer cell migration | |
Development of first-in-class dual Sirt2/HDAC6 inhibitors as molecular tools for dual inhibition of tubulin deacetylation | |
Development of new strategies for specific inhibition of human histone deacetylase 8 | |
Drug discovery from African medicinal plants : natural product database development, lead discovery and toxicity assessment ; kumulative Habilitationsschrift | |
Effects of environmental conditions on nephron number: modeling maternal disease and epigenetic regulation in renal development | |
Entwicklung neuer Strategien zur spezifischen Hemmung humaner Histondeacetylase 8 | |
Epigenetic targets in drug discovery | |
First fluorescent acetylspermidine deacetylation assay for HDAC10 identifies selective inhibitors with cellular target engagement | |
HDAC8 : a multifaceted target for therapeutic interventions | |
Histone acetyltransferase inhibitors block neuroblastoma cell growth in vivo | |
How to separate kinase inhibition from undesired monoamine oxidase a inhibition - the development of the DYRK1A inhibitor AnnH75 from the alkaloid harmine | |
Identification of bichalcones as sirtuin inhibitors by virtual screening and in vitro testing | |
A kinome-wide RNAi screen identifies ALK as a target to sensitize neuroblastoma cells for HDAC8-inhibitor treatment | |
Molecular modeling : basic principles and applications | |
Molecular Modelling Untersuchungen zum Bindungsverhalten von Histamin H2- und H3-Rezeptor-Liganden | |
Neuartige Kinaseinhibitoren zur multitargeted Therapie der Alzheimer-Krankheit | |
Novel effective small-molecule inhibitors of protein kinases related to tau pathology in Alzheimer’s disease | |
Pharmacoinformatic investigation of medicinal plants from East Africa | |
potential for histone deacetylase (HDAC) inhibitors as cestocidal drugs | |
Proteolysis targeting chimeras (PROTACs) for epigenetics research | |
Rational approaches to drug design : proceedings of the | |
Selective Sirt2 inhibition by ligand-induced rearrangement of the active site | |
Selectivity Profiling and Biological Activity of Novel β-Carbolines as Potent and Selective DYRK1 Kinase Inhibitors | |
Sirtuin 1 inhibiting thiocyanates (S1th) - a new class of isotype selective inhibitors of NAD+ dependent lysine deacetylases | |
Structural basis for the inhibition of histone deacetylase 8 (HDAC8), a key epigenetic player in the blood fluke schistosoma mansoni | |
Structure-based design, docking and binding free energy calculations of A366 derivatives as spindlin1 inhibitors | |
Structure-based design of inhibitors of the zinc-dependent enzymes histone deacetylase (HDAC) and UDP-3-O-(R-3-hydroxymyristoylyl)-N-acetylglucosamine deacetylase (LpxC) | |
Structure‐based design, synthesis, and biological evaluation of triazole‐based smHDAC8 inhibitors | |
Synthesis and biological characterization of novel inhibitors of histone deacetylases as anticancer and antiparasitic agents [Kumulative Dissertation] | |
Untersuchungen zur Synthese und biochemischen Charakterisierung von subtypselektiven Inhibitoren der humanen Histondeacetylasen HDAC8 und 10 | |
Virtual screening and molecular modeling studies applied to discover novel sirtuin modulators and cholinesterase inhibitors : [kumulative Dissertation] |