Improvements in the efficacy and spectrum of the spinosyns, novel fermentation derived insecticide, has long been a goal within Dow AgroSciences. As large and complex fermentation products identifying specific modifications to the spinosyns likely to result in improved activity was a difficult process, since most modifications decreased the activity. A variety of approaches were investigated to identify new synthetic directions for the spinosyn chemistry including several explorations of the quantitative structure activity relationships (QSAR) of spinosyns, which initially were unsuccessful. However, application of artificial neural networks (ANN) to the spinosyn QSAR problem identified new directions for improved activity in the chemistry, which subsequent synthesis and testing confirmed. The ANN-based analogs coupled with other information on substitution effects resulting from spinosyn structure activity relationships lead to the discovery of spinetoram (XDE-175). Launched in late 2007, spinetoram provides both improved efficacy and an expanded spectrum while maintaining the exceptional environmental and toxicological profile already established for the spinosyn chemistry.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1007/s10822-008-9205-8 | DOI Listing |
Pest Manag Sci
August 2021
Corteva Agriscience, Discovery Research, Indianapolis, IN, USA.
Natural products (NPs) have long been a source of insecticidal crop protection products. Like many macrolide NPs, the spinosyns originated from a soil inhibiting microorganism (Saccharopolyspora spinosa). More than 20 years after initial registration, the spinosyns remain a unique class of NP-based insect control products that presently encompass two insecticidal active ingredients, spinosad, a naturally occurring mixture of spinosyns, and spinetoram, a semi-synthetic spinosyn product.
View Article and Find Full Text PDFJ Ind Microbiol Biotechnol
March 2016
Dow AgroSciences LLC, 9330 Zionsville Road, Indianapolis, IN, 46268, USA.
This review highlights the importance of natural product research and industrial microbiology for product development in the agricultural industry, based on examples from Dow AgroSciences. It provides an overview of the discovery and development of spinetoram, a semisynthetic insecticide derived by a combination of a genetic block in a specific O-methylation of the rhamnose moiety of spinosad coupled with neural network-based QSAR and synthetic chemistry. It also emphasizes the key role that new technologies and multidisciplinary approaches play in the development of current spinetoram production strains.
View Article and Find Full Text PDFInsect Biochem Mol Biol
May 2010
Dow AgroSciences LLC, Discovery Research, 9330 Zionsville Road, Indianapolis, IN 46268, USA.
Strains of Drosophila melanogaster with resistance to the insecticides spinosyn A, spinosad, and spinetoram were produced by chemical mutagenesis. These spinosyn-resistant strains were not cross-resistant to other insecticides. The two strains that were initially characterized were subsequently found to have mutations in the gene encoding the nicotinic acetylcholine receptor (nAChR) subunit Dalpha6.
View Article and Find Full Text PDFJ Comput Aided Mol Des
August 2008
Dow AgroSciences, Discovery Research, 9330 Zionsville Road, Bldg. 306/G1, Indianapolis, IN, 46268, USA.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!