Sebastian Oddsson

Sebastian Oddsson

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article

Previous Organizations / Institutes

The organizations / institutes from the scholar's other articles in the past ten years


Sebastian Oddsson has a total of 8 co-authors. Here are the top co-authors by number of shared publications:

  • Christian Trachsel

    Functional Genomics Center Zürich, ETH Zürich/University of Zürich, CH-8057 Zürich, Switzerland

    1 shared publication
  • D�Niel Ï¿½ Carrera

    Institute for Agricultural Sciences, Plant Biochemistry, ETH Z�rich, CH-8092 Z�rich, Switzerland

    1 shared publication
  • Elin Soffia Olafsdottir

    Faculty of Pharmaceutical Sciences, University of Iceland, Hofsvallagata 53, IS-107 Reykjavik, Iceland

    1 shared publication
  • Jonas Grossmann

    Functional Genomics Center Zürich, ETH Zürich/University of Zürich, CH-8057 Zürich, Switzerland

    1 shared publication
  • Natalia M. Kowal

    Faculty of Pharmaceutical Sciences, School of Health Sciences, University of Iceland, 107 Reykjavík, Iceland

    1 shared publication
  • Philip K. Ahring

    School of Medical Sciences, Faculty of Medicine and Health, Brain and Mind Centre, The University of Sydney, Sydney, NSW, 2050, Australia

    1 shared publication

Latest Publications

  • Open Access

    Structure-Based Discovery of Dual-Target Hits for Acetylcholinesterase and the α7 Nicotinic Acetylcholine Receptors: In Silico Studies and In Vitro Confirmation

    by Sebastian Oddsson, Natalia M. Kowal, Philip K. Ahring, Elin S. Olafsdottir, Thomas Balle

    Despite extensive efforts in the development of drugs for complex neurodegenerative diseases, treatment often remains challenging or ineffective, and hence new treatment strategies are necessary. One approach is the design of multi-target drugs, which can potentially address the complex nature of disorders such as Alzheimer’s disease. We report a method for high throughput virtual screening aimed at identifying new dual target hit molecules. One of the identified hits, N,N-dimethyl-1-(4-(3-methyl-[1,2,4]triazolo[4,3-a]pyrimidin-6-yl)phenyl)ethan-1-amine (Ýmir-2), has dual-activity as an acetylcholinesterase (AChE) inhibitor and as an α7 nicotinic acetylcholine receptor (α7 nAChR) agonist. Using computational chemistry methods, parallel and independent screening of a virtual compound library consisting of 3,848,234 drug-like and commercially available molecules from the ZINC15 database, resulted in an intersecting set of 57 compounds, that potentially possess activity at both of the two protein targets. Based on ligand efficiency as well as scaffold and molecular diversity, 16 of these compounds were purchased for in vitro validation by Ellman’s method and two-electrode voltage-clamp electrophysiology. Ýmir-2 was shown to exhibit the desired activity profile (AChE IC50 = 2.58 ± 0.96 µM; α7 nAChR activation = 7.0 ± 0.9% at 200 µM) making it the first reported compound with this particular profile and providing further evidence of the feasibility of in silico methods for the identification of novel multi-target hit molecules.


  • Comparative Proteomic Analysis of Plant Acclimation to Six Different Long-Term Environmental Changes

    by D�Niel Ï¿½ Carrera, Sebastian Oddsson, Jonas Grossmann, Christian Trachsel, Sebastian Streb

    Plants are constantly challenged in their natural environment by a range of changing conditions. We investigated the acclimation processes and adaptive plant responses to various long-term mild changes and compared them directly within one experimental set-up. Arabidopsis thaliana plants were grown in hydroponic culture for 10 d under controlled abiotic stress (15°C, 25°C, salt and osmotic) and in nutrient deficiency (nitrate and phosphate). Plant growth was monitored and proteomic experiments were performed. Resource allocation between tissues altered during the plants’ response. The growth patterns and induced changes of the proteomes indicated that the underlying mechanisms of the adaptation processes are highly specific to the respective environmental condition. Our results indicated differential regulation of response to salt and osmotic treatment, while the proteins in the changed temperature regime showed an inverse, temperature-sensitive control. There was a high correlation of protein level between the nutrient-deficient treatments, but the enriched pathways varied greatly. The proteomic analysis also revealed new insights into the regulation of proteins specific to the shoot and the root. Our investigation revealed unique strategies of plant acclimation to the different applied treatments on a physiological and proteome level, and these strategies are quite distinct in tissues below and above ground.