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Design and Validation of FRESH, a Drug Discovery Paradigm Resting on Robust Chemical Synthesis
- Source :
- ACS Medicinal Chemistry Letters. 6:518-522
- Publication Year :
- 2015
- Publisher :
- American Chemical Society (ACS), 2015.
-
Abstract
- A method capable of identifying novel synthetic targets for small molecule lead optimization has been developed. The FRESH (FRagment-based Exploitation of modular Synthesis by vHTS) approach relies on a multistep synthetic route to a target series of compounds devised by a close collaboration between synthetic and computational chemists. It combines compound library generation, quantitative structure-acitvity relationship construction, fragment processing, virtual high throughput screening and display of results within the Pipeline Pilot framework. Outcomes enumerate tailored selection of novel synthetic targets with improved potency and optimized physical properties for an emerging compound series. To validate the application of FRESH, three retrospective case studies have been performed to pinpoint reported potent analogues. One prospective case study was performed to demonstrate that FRESH is able to capture additional potent analogues.
- Subjects :
- Quantitative structure–activity relationship
business.industry
Computer science
Drug discovery
High-throughput screening
Pipeline (computing)
Organic Chemistry
Modular design
Biochemistry
Combinatorial chemistry
Fragment (logic)
Fragment processing
Drug Discovery
Biochemical engineering
business
ADME
Subjects
Details
- ISSN :
- 19485875
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- ACS Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....5efb01e0480cb47baa043f732481f144
- Full Text :
- https://doi.org/10.1021/acsmedchemlett.5b00062