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

AI Article Synopsis

  • The EU-OPENSCREEN initiative was established to enhance the discovery of new molecular research tools and drug candidates by combining the expertise and resources of 20 European partners in chemical biology.* -
  • Recent projects demonstrated successful outcomes, including promising compounds for antimalarial drugs, apoptosis-inducing peptides for specific cancer types, small-molecule ROCK inhibitors for regenerative applications, and novel treatments for metabolic disorders and acute myeloid leukemia.* -
  • These findings emphasize the advantages of small-molecule screening and the collaboration between medicinal chemistry and various assay designs facilitated by EU-OPENSCREEN.*

Article Abstract

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(3 H)-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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764006PMC
http://dx.doi.org/10.1177/2472555218816276DOI Listing

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