<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tredup C</submitter><funding>Bristol-Myers Squibb</funding><funding>Pfizer</funding><funding>Bayer</funding><funding>Royal Institution for the Advancement of Learning McGill University</funding><funding>Ontario Institute for Cancer Research</funding><funding>Genentech</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Horizon 2020 Framework Programme</funding><funding>Takeda Pharmaceutical Company</funding><funding>Kungliga Tekniska Hoegskolan</funding><funding>Deutschen Konsortium für Translationale Krebsforschung</funding><funding>Boehringer Ingelheim</funding><funding>Innovative Health Initiative</funding><funding>Merck KGaA</funding><funding>LOEWE Zentrum AdRIA</funding><funding>Diamond Light Source</funding><funding>Genome Canada</funding><funding>Janssen Pharmaceuticals</funding><pagination>822-836</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10127199</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(4)</volume><pubmed_abstract>Well-characterized small molecules are essential tools for studying the biology and therapeutic relevance of a target protein. However, many compounds reported in the literature and routinely studied in biomedical research lack the potency and selectivity required for mechanistic cellular studies on the function of a given protein. Furthermore, commercially available compounds often do not include useful tools developed by industry as part of their research and development efforts, as they frequently remain proprietary. The freely available donated chemical probe (DCP) library, fueled by generous donations of compounds from industry and academia, enables easy access to a steadily growing collection of these valuable and well-characterized tools. Here, we provide a systematic description of</pubmed_abstract><journal>ACS chemical biology</journal><pubmed_title>Deep Annotation of Donated Chemical Probes (DCP) in Organotypic Human Liver Cultures and Patient-Derived Organoids from Tumor and Normal Colorectum.</pubmed_title><pmcid>PMC10127199</pmcid><funding_grant_id>875510</funding_grant_id><funding_grant_id>1399</funding_grant_id><funding_grant_id>INST 161/920-1 FUGG</funding_grant_id><funding_grant_id>1177</funding_grant_id><funding_grant_id>III L 5 - 519/03/03.001 - (0015)</funding_grant_id><pubmed_authors>Tredup C</pubmed_authors><pubmed_authors>Knapp S</pubmed_authors><pubmed_authors>Berger BT</pubmed_authors><pubmed_authors>Muller S</pubmed_authors><pubmed_authors>Tjaden A</pubmed_authors><pubmed_authors>Rohm S</pubmed_authors><pubmed_authors>Youhanna S</pubmed_authors><pubmed_authors>Farin HF</pubmed_authors><pubmed_authors>Berger LM</pubmed_authors><pubmed_authors>Kramer A</pubmed_authors><pubmed_authors>Ndreshkjana B</pubmed_authors><pubmed_authors>Schneider NS</pubmed_authors><pubmed_authors>Lauschke VM</pubmed_authors><pubmed_authors>Kemas AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deep Annotation of Donated Chemical Probes (DCP) in Organotypic Human Liver Cultures and Patient-Derived Organoids from Tumor and Normal Colorectum.</name><description>Well-characterized small molecules are essential tools for studying the biology and therapeutic relevance of a target protein. However, many compounds reported in the literature and routinely studied in biomedical research lack the potency and selectivity required for mechanistic cellular studies on the function of a given protein. Furthermore, commercially available compounds often do not include useful tools developed by industry as part of their research and development efforts, as they frequently remain proprietary. The freely available donated chemical probe (DCP) library, fueled by generous donations of compounds from industry and academia, enables easy access to a steadily growing collection of these valuable and well-characterized tools. Here, we provide a systematic description of</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2026-05-29T03:15:31.493Z</modification><creation>2024-12-04T10:47:34.207Z</creation></dates><accession>S-EPMC10127199</accession><cross_references><pubmed>36944371</pubmed><doi>10.1021/acschembio.2c00877</doi></cross_references></HashMap>