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Idler Compounds: A Simple Protocol for Openly Sharing Fridge Contents for Cross-Screening
Rebecka Isaksson1, Eve M Carter1, Charlotte K Hind2
1School of Pharmacy and Structural Genomics Consortium, University College London, 29-39 Brunswick Square, London WC1N 1AX, U.K.
Academic drug discovery labs can unlock valuable compounds by creating open libraries of "idlers" – molecules not actively pursued. Screening these libraries against new targets, like pathogens, maximizes resource utility and promotes open science for novel research.
Area of Science:
- Drug discovery
- Chemical biology
- Open science
Background:
- Academic drug discovery labs accumulate large compound collections that are often underutilized.
- Cross-screening compound libraries against alternative targets offers potential for novel hit identification.
- Sharing and utilizing these academic compound collections is infrequent.
Purpose of the Study:
- To provide a guide for establishing open compound libraries from underutilized academic small molecules.
- To demonstrate the screening of such a library against a panel of pathogens.
- To encourage the broader adoption of open science principles in academic drug discovery.
Main Methods:
- Identification and collection of "idler" compounds not actively pursued in research projects.
- Creation of a diverse subset from the collected idler compounds.
- Screening of the compound subset against a panel of pathogenic targets.
- Public dissemination of screening data.
Main Results:
- A diverse subset of the open compound library was successfully screened against pathogens.
- Screening data was made publicly available, enabling further research.
- The process demonstrated a viable method for repurposing underutilized academic compound collections.
Conclusions:
- Establishing open compound libraries from academic "idlers" maximizes resource utility.
- Publicly sharing screening data catalyzes novel research and insights.
- This approach promotes open science and efficient drug discovery.
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