2005Angewandte Chemie International EditionRequires access

Cellular Profiling of Small‐Molecule Bioactivities: an Alternative Tool for Chemical Biology

Thorsten Berg

Open publisher page 5 citations

Abstract

Are they a good match? Target identification is critical to the success of chemical genetics projects that start with phenotypic screens. The method highlighted herein is a novel way to decrease the number of potential biological targets of compounds identified in phenotypic screens by comparison of their cellular activity profiles with those obtained with reference compounds. Activity profiles for hypothetical compounds A and B are shown.

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What this paper is about

Are they a good match? Target identification is critical to the success of chemical genetics projects that start with phenotypic screens. The method highlighted herein is a novel way to decrease the number of potential biological targets of compounds identified in phenotypic screens by comparison of their cellular activity profiles with those obtained with reference compounds. Activity profiles for hypothetical compounds A and B are shown.

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OpenAlex reports 5 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Are they a good match? Target identification is critical to the success of chemical genetics projects that start with phenotypic screens. The method highlighted herein is a novel way to decrease the number of potential biological targets of compounds identified in phenotypic screens by comparison of their cellular activity profiles with those obtained with reference compounds. Activity profiles for hypothetical compounds A and B are shown.

Key concepts: Profiling (computer programming), Computational biology, Phenotype, Small molecule, Chemical biology, Chemical genetics, Identification (biology), Phenotypic screening

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