The Unique Role of Fluorine in the Design of Active Ingredients for Modern Crop Protection
Top Cited Papers
- 28 April 2004
- journal article
- review article
- Published by Wiley in ChemBioChem
- Vol. 5 (5), 570-589
- https://doi.org/10.1002/cbic.200300833
Abstract
The task of inventing and developing active ingredients with useful biological activities requires a search for novel chemical substructures. This process may trigger the discovery of whole classes of chemicals of potential commercial interest. Similar biological effects can often be achieved by completely different compounds. However, compounds within a given structural family may exhibit quite different biological activities depending on their interactions with different intracellular proteins like enzymes or receptors. By varying the functional groups and structural elements of a lead compound, its interaction with the active site of the target protein, as well as its physicochemical, pharmacokinetic, and dynamic properties can be improved. In this context, the introduction of fluorine into active ingredients has become an important concept in the quest for a modern crop protection product with optimal efficacy, environmental safety, user friendliness, and economic viability. Fluorinated organic compounds represent an important and growing family of commercial agrochemicals. A number of recently developed agrochemical candidates represent novel classes of chemical compounds with new modes of action; several of these compounds contain new fluorinated substituents. However, the complex structure–activity relationships associated with biologically active molecules mean that the introduction of fluorine can lead to either an increase or a decrease in the efficacy of a compound depending on its changed mode of action, physicochemical properties, target interaction, or metabolic susceptibility and transformation. Therefore, it is still difficult to predict the sites in a molecule at which fluorine substitution will result in optimal desired effects.Keywords
This publication has 51 references indexed in Scilit:
- Research into fluorinated pyrethroid alcohols-an episode in the history of pyrethroid discoveryPesticide Science, 1998
- Crystal structrure of herbicide-detoxifying maize glutathione S-transferase-I in complex with lactoylglutathione: evidence for an induced-fit mechanismJournal of Molecular Biology, 1997
- A New Binding Model for Structurally Diverse ALS InhibitorsPesticide Science, 1996
- Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94Journal of Computational Chemistry, 1996
- Biological activity of flucycloxuron, a novel benzoylphenylurea derivative, onTenebrio molitor: comparison with diflubenzuron and triflumuronCellular and Molecular Life Sciences, 1993
- Synthesis of 1,2,4‐triazole compounds related to the fungicides flutriafol and hexaconazolePesticide Science, 1991
- Herbicides inhibiting branched‐chain amino acid biosynthesisPesticide Science, 1990
- The inhibition of chitin synthesis in spodoptera littoralis larvae by flufenoxuron, teflubenzuron and diflubenzuronPesticide Science, 1990
- Organosilane insecticides. Part II: Chemistry and structure—activity relationshipsPesticide Science, 1990
- Oudemansin, strobilurin A, strobilurin B and myxothiazol: new inhibitors of the bc1 segment of the respiratory chain with an E‐β‐methoxyacrylate system as common structural elementFEBS Letters, 1981