Počet záznamů: 1  

EU-OPENSCREEN: A Novel Collaborative Approach to Facilitate Chemical Biology

  1. 1.
    0506196 - ÚMG 2020 RIV US eng J - Článek v odborném periodiku
    Brennecke, P. - Rasina, D. - Aubi, O. - Herzog, K. - Landskron, J. - Cautain, B. - Vicente, F. - Quintana, J. - Mestres, J. - Stechmann, B. - Ellinger, B. - Brea, J. - Kolanowski, J. L. - Pilarski, R. - Orzaez, M. - Pineda-Lucena, A. - Laraia, L. - Nami, F. - Zielenkiewicz, P. - Paruch, K. - Hansen, E. - von Kries, J.P. - Neuenschwander, M. - Specker, E. - Bartůněk, Petr - Šímová, Šárka - Lesnikowski, Z. - Krauss, S. - Lehtio, L. - Bilitewski, U. - Broenstrup, M. - Tasken, K. - Jirgensons, A. - Lickert, H. - Clausen, M. H. - Andersen, J. H. - Vicent, M. J. - Genilloud, O. - Martinez, A. - Nazare, M. - Fecke, W. - Gribbon, P.
    EU-OPENSCREEN: A Novel Collaborative Approach to Facilitate Chemical Biology.
    SLAS Discovery. Roč. 24, č. 3 (2019), s. 398-413. ISSN 2472-5552. E-ISSN 2472-5560
    Grant CEP: GA MŠMT LO1220; GA MŠMT LM2015063
    Institucionální podpora: RVO:68378050
    Klíčová slova: chemical biology * screening * medicinal chemistry * open access * compound library
    Obor OECD: Biochemical research methods
    Impakt faktor: 2.195, rok: 2019
    Způsob publikování: Open access
    https://journals.sagepub.com/doi/10.1177/2472555218816276

    Compound screening in biological assays and subsequent optimization of hits is indispensable for the development of new molecular research tools and drug candidates. To facilitate such discoveries, the European Research Infrastructure EU-OPENSCREEN was founded recently with the support of its member countries and the European Commission. Its distributed character harnesses complementary knowledge, expertise, and instrumentation in the discipline of chemical biology from 20 European partners, and its open working model ensures that academia and industry can readily access EU-OPENSCREEN's compound collection, equipment, and generated data. To demonstrate the power of this collaborative approach, this perspective article highlights recent projects from EU-OPENSCREEN partner institutions. These studies yielded (1) 2-aminoquinazolin-4(3H)-ones as potential lead structures for new antimalarial drugs, (2) a novel lipodepsipeptide specifically inducing apoptosis in cells deficient for the pVHL tumor suppressor, (3) small-molecule-based ROCK inhibitors that induce definitive endoderm formation and can potentially be used for regenerative medicine, (4) potential pharmacological chaperones for inborn errors of metabolism and a familiar form of acute myeloid leukemia (AML), and (5) novel tankyrase inhibitors that entered a lead-to-candidate program. Collectively, these findings highlight the benefits of small-molecule screening, the plethora of assay designs, and the close connection between screening and medicinal chemistry within EU-OPENSCREEN.
    Trvalý link: http://hdl.handle.net/11104/0297510

     
     
Počet záznamů: 1  

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