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Published on: April 30, 2018
Combinatorial chemistry in the agrosciences
Stephen D Lindell1, Lisa C Pattenden, Jonathan Shannon
1Bayer CropScience AG, Werk Höchst, G836, D-65926 Frankfurt am Main, Germany. stephen.lindell@bayercropscience.com
Combinatorial chemistry accelerates the discovery of new agrochemicals like fungicides, herbicides, and insecticides. This review highlights key methods including bioavailability and virtual screening for designing effective compound libraries.
Area of Science:
- Agrochemical research
- Medicinal chemistry
- Drug discovery
Background:
- Combinatorial chemistry and high-throughput screening have transformed agrochemical lead discovery.
- Traditional methods are being augmented by advanced techniques for identifying new active compounds.
Purpose of the Study:
- To review recent applications of combinatorial synthesis in discovering new fungicides, herbicides, and insecticides.
- To discuss the impact of various design strategies on compound library development.
Main Methods:
- Review of recent literature on combinatorial synthesis in agrochemical research.
- Discussion of factors influencing compound library design, including bioavailability, natural products, privileged structures, virtual screening, and protein crystallography.
Main Results:
- Combinatorial synthesis is a key driver in the lead discovery process for agrochemicals.
- The integration of bioavailability guidelines, natural products, privileged structures, virtual screening, and structural data enhances library design.
Conclusions:
- Combinatorial chemistry and high-throughput screening are essential for modern agrochemical discovery.
- Strategic design of compound libraries, informed by diverse data sources, is crucial for identifying novel fungicides, herbicides, and insecticides.
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