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Development of a chemogenomics library for phenotypic screening.
Dafniet, Bryan; Cerisier, Natacha; Boezio, Batiste; Clary, Anaelle; Ducrot, Pierre; Dorval, Thierry; Gohier, Arnaud; Brown, David; Audouze, Karine; Taboureau, Olivier.
Afiliación
  • Dafniet B; Université de Paris, INSERM U1133, CNRS UMR8251, 75006, Paris, France.
  • Cerisier N; Université de Paris, INSERM U1133, CNRS UMR8251, 75006, Paris, France.
  • Boezio B; Université de Paris, INSERM U1133, CNRS UMR8251, 75006, Paris, France.
  • Clary A; Institut de Recherche Servier, 125 Chemin de Ronde, 78290, Croissy-sur-Seine, France.
  • Ducrot P; Institut de Recherche Servier, 125 Chemin de Ronde, 78290, Croissy-sur-Seine, France.
  • Dorval T; Institut de Recherche Servier, 125 Chemin de Ronde, 78290, Croissy-sur-Seine, France.
  • Gohier A; Institut de Recherche Servier, 125 Chemin de Ronde, 78290, Croissy-sur-Seine, France.
  • Brown D; Institut de Recherche Servier, 125 Chemin de Ronde, 78290, Croissy-sur-Seine, France.
  • Audouze K; Université de Paris, INSERM UMR S-1124, 75006, Paris, France.
  • Taboureau O; Université de Paris, INSERM U1133, CNRS UMR8251, 75006, Paris, France. olivier.taboureau@u-paris.fr.
J Cheminform ; 13(1): 91, 2021 Nov 24.
Article en En | MEDLINE | ID: mdl-34819133
ABSTRACT
With the development of advanced technologies in cell-based phenotypic screening, phenotypic drug discovery (PDD) strategies have re-emerged as promising approaches in the identification and development of novel and safe drugs. However, phenotypic screening does not rely on knowledge of specific drug targets and needs to be combined with chemical biology approaches to identify therapeutic targets and mechanisms of actions induced by drugs and associated with an observable phenotype. In this study, we developed a system pharmacology network integrating drug-target-pathway-disease relationships as well as morphological profile from an existing high content imaging-based high-throughput phenotypic profiling assay known as "Cell Painting". Furthermore, from this network, a chemogenomic library of 5000 small molecules that represent a large and diverse panel of drug targets involved in diverse biological effects and diseases has been developed. Such a platform and a chemogenomic library could assist in the target identification and mechanism deconvolution of some phenotypic assays. The usefulness of the platform is illustrated through examples.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Screening_studies Idioma: En Revista: J Cheminform Año: 2021 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Screening_studies Idioma: En Revista: J Cheminform Año: 2021 Tipo del documento: Article País de afiliación: Francia