Pydiflumetofen Explained

Pydiflumetofen is a broad spectrum fungicide used in agriculture to protect crops from fungal diseases. It was first marketed by Syngenta in 2016 using their brand name Miravis. The compound is an amide which combines a pyrazole acid with a substituted phenethylamine to give an inhibitor of succinate dehydrogenase,[1] an enzyme that inhibits cellular respiration in almost all living organisms.[2]

History

Inhibition of succinate dehydrogenase, the complex II in the mitochondrial respiration chain, has been known as a fungicidal mechanism of action since the first examples were marketed in the 1960s. The first compound in this class was carboxin, which had a narrow spectrum of useful biological activity, mainly on basidiomycetes and was used as a seed treatment.[3] [4] By 2016, at least 17 further examples of this mechanism of action were developed by crop protection companies, with the market leader being boscalid, owing to its broader spectrum of fungal species controlled. However, it lacked full control of important cereal diseases, especially septoria leaf blotch Zymoseptoria tritici.[3] A group of compounds which did control septoria were amides of pyrazole-4-carboxylic acid, with the most successful being derivatives with an N-methyl group and a difluromethyl group in position 3 of the ring. These include penthiopyrad and fluxapyroxad.[5] Research chemists at Syngenta made many analogues of this type[6] in the search for new products and by 2008 had discovered benzovindiflupyr, isopyrazam, sedaxane and pydiflumetofen.[3]

Synthesis

Pydiflumetofen combines 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid with a novel amine derivative which was made from 2,4,6-trichlorobenzaldehyde.[7]

A nitrostyrene is formed in a Henry reaction between the aldehyde and nitroethane. A reduction reaction converts it to a ketone which forms an imine with methoxyamine. This, in turn, is reduced with sodium cyanoborohydride to give the amine required for amide formation with the acid chloride of the pyrazole.[7]

Mechanism of action

Succinate dehydrogenase inhibitors (SDHI) of this type act by binding at the quinone reduction site of the enzyme complex, preventing ubiquinone from doing so. As a consequence, the tricarboxylic acid cycle and electron transport chain cannot function.[8] [9] [10]

Usage

Pydiflumetofen has fungicidal effects against a wide range of crop pests. These include Alternaria, grey mould (Botrytis cinerea), Cercospora (leaf spot), septoria, powdery mildews (e.g. Uncinula necator), and scab (e.g. Venturia pyrina). As a result, it has potential use in crops including cereals, corn, soybeans, vegetables, peanut, curcubits, potato and fruit.[11] [12] [13] The compound was introduced in the US in 2018 but estimated usage that year was low at only 4000lb.[14] The compound is registered for use on peanut and fruits.[13] the compound is also registered in Argentina, Australia, Canada and New Zealand.[15]

Human safety

Pydiflumetofen has low acute toxicity:[10] the Codex Alimentarius database maintained by the FAO lists the maximum residue limits for it in various food products.[16]

Environmental effects

The compound is very persistent in field conditions and its environmental fate and consequent ecotoxicology have been reviewed.[10] In one laboratory study, the R enantiomer of the compound was shown to be more toxic to Zebrafish, which was interpreted to be owing to its higher potency as an SDHI inhibitor than the S isomer.[17] [18]

Resistance management

Fungal populations have the ability to develop resistance to SDHI inhibitors.[19] This potential can be mitigated by careful management. Reports of individual pest species becoming resistant are monitored by manufacturers, regulatory bodies such as the EPA and the Fungicides Resistance Action Committee (FRAC).[20] The risks of resistance developing can be reduced by using a mixture of two or more fungicides which each have activity on relevant pests but with unrelated mechanisms of action. FRAC assigns fungicides into classes so as to facilitate this.[21]

Brands

Pydiflumetofen is the ISO common name[22] for the active ingredient which is formulated into the branded product sold to end-users. Miravis is the brand name for Syngenta's suspension concentrate, which it also calls Adepidyn technology.[13] [15] The Miravis brand line includes other products containing pydiflumetofen mixed with other fungicidal active ingredients. These include Miravis Duo and Miravis Top (containing difenoconazole), Miravis Neo (containing propiconazole and azoxystrobin), and Miravis SBX (containing difenoconazole and azoxystrobin).[23]

Trebuset is the brand name for Syngenta's flowable concentrate formulation for use as a seed treatment.[24]

Further reading

External links

Notes and References

  1. Web site: Pydiflumetofen . Makoto . Irie . 2017 . 2023-07-27 . .
  2. 10.1371/journal.pone.0224132 . free . Evolutionarily conserved susceptibility of the mitochondrial respiratory chain to SDHI pesticides and its consequence on the impact of SDHIs on human cultured cells . 2019 . Bénit . Paule . Kahn . Agathe . Chretien . Dominique . Bortoli . Sylvie . Huc . Laurence . Schiff . Manuel . Gimenez-Roqueplo . Anne-Paule . Favier . Judith . Gressens . Pierre . Rak . Malgorzata . Rustin . Pierre . 3 . PLOS ONE . 14 . 11 . e0224132 . 31697708 . 6837341 . 2019PLoSO..1424132B .
  3. Book: 10.1002/9783527693931.ch31 . Fungicidal Succinate-Dehydrogenase-Inhibiting Carboxamides . Bioactive Carboxylic Compound Classes: Pharmaceuticals and Agrochemicals . 2016 . Walter . Harald . Lamberth . Clemens . Jürgen . Dinges . Wiley . 405–425 . 978-3-527-33947-1 .
  4. Web site: History of SDHI-fungicides . frac.info . 2023-07-26 .
  5. Web site: Pyrazolecarboxamide fungicides . 2023-07-27 . BCPC.
  6. 10.1007/s00706-017-2101-y . Synthesis of fungicidally active succinate dehydrogenase inhibitors with novel difluoromethylated heterocyclic acid moieties . 2018 . Walter . Harald . Lamberth . Clemens . Corsi . Camilla . Monatshefte für Chemie - Chemical Monthly . 149 . 4 . 791–799 . 103548298 .
  7. US . 8258169 . patent . Pyrazole-4-N-alkoxycarboxamides as microbiocides . 2012-09-04 . 2009-12-01 . 2008-12-05 . Rajan, R . Walter, H . Stierli, D . Syngenta Crop Protection .
  8. 10.1074/jbc.M311876200 . free . The Quaternary Structure of the Saccharomyces cerevisiae Succinate Dehydrogenase . 2004 . Oyedotun . Kayode S. . Lemire . Bernard D. . Journal of Biological Chemistry . 279 . 10 . 9424–9431 . 14672929 .
  9. 10.1016/j.cropro.2010.02.019 . Progress in understanding molecular mechanisms and evolution of resistance to succinate dehydrogenase inhibiting (SDHI) fungicides in phytopathogenic fungi . 2010 . Avenot . Hervé F. . Michailides . Themis J. . Crop Protection . 29 . 7 . 643–651 . 2010CrPro..29..643A .
  10. 10.2903/j.efsa.2019.5821 . free . Peer review of the pesticide risk assessment of the active substance pydiflumetofen . 2019 . Arena . Maria . Auteri . Domenica . Brancato . Alba . Bura . Laszlo . Carrasco Cabrera . Luis . Chaideftou . Eugenia . Chiusolo . Arianna . Court Marques . Daniele . Crivellente . Federica . De Lentdecker . Chloe . Egsmose . Mark . Fait . Gabriella . Ferreira . Lucien . Greco . Luna . Ippolito . Alessio . Istace . Frederique . Jarrah . Samira . Kardassi . Dimitra . Leuschner . Renata . Lostia . Alfonso . Lythgo . Christopher . Mangas . Iris . Miron . Ileana . Molnar . Tunde . Padovani . Laura . Parra Morte . Juan Manuel . Pedersen . Ragnor . Reich . Hermine . Santos . Miguel . Serafimova . Rositsa . EFSA Journal . 17 . 10 . e05821 . 32626121 . 7008818 . 3 .
  11. 10.1016/j.pestbp.2019.06.017 . Bioactivity, physiological characteristics and efficacy of the SDHI fungicide pydiflumetofen against Sclerotinia sclerotiorum . 2019 . Huang . Xue-Ping . Luo . Jian . Li . Bei-Xing . Song . Yu-fei . Mu . Wei . Liu . Feng . Pesticide Biochemistry and Physiology . 160 . 70–78 . 31519259 . 198268036 .
  12. 10.1094/pdis-05-18-0763-re . Pharmacological Characteristics and Control Efficacy of a Novel SDHI Fungicide Pydiflumetofen Against Sclerotinia sclerotiorum . 2019 . Duan . Yabing . Xiu . Qian . Li . Haoran . Li . Tao . Wang . Jianxin . Zhou . Mingguo . Plant Disease . 103 . 1 . 77–82 . 30358507 . 53022480 . free .
  13. Web site: Miravis fungicide . 2023-07-27 . Syngenta US . 2021.
  14. Web site: Estimated Agricultural Use for pydiflumetofen, 2018 . US Geological Survey . 2021-10-12 . 2023-07-26 .
  15. Web site: ADEPIDYN® technology . 2023-07-27 . syngenta.com.
  16. Web site: Pydiflumetofen . FAO / WHO .
  17. 10.1016/j.envint.2022.107406 . Comprehensive study of pydiflumetofen in Danio rerio: Enantioselective insight into the toxic mechanism and fate . 2022 . Wang . Zhen . Tan . Yuting . Li . Yanhong . Duan . Jinsheng . Wu . Qiqi . Li . Rui . Shi . Haiyan . Wang . Minghua . Environment International . 167 . 107406 . 35850082 . 2022EnInt.16707406W. 250463420 .
  18. 10.1002/ps.6389 . Evaluation of exploitive potential for higher bioactivity and lower residue risk enantiomer of chiral fungicide pydiflumetofen . 2021 . Wang . Zhen . Li . Rui . Zhang . Jing . Liu . Shiling . He . Zongzhe . Wang . Minghua . Pest Management Science . 77 . 7 . 3419–3426 . 33797181 . 232763150 .
  19. 10.1094/pdis-03-20-0487-re . Identification and Characterization of Fungicide Resistance in Botrytis Populations from Small Fruit Fields in the Mid-Atlantic United States . 2021 . Cosseboom . Scott . Hu . Mengjun . Plant Disease . 105 . 9 . 2366–2373 . 33719541 . 232231834 . free .
  20. Web site: Fungicides Resistance Action Committee website.
  21. Web site: Search Fungicides to find FRAC Recommendations . 2020-09-04 .
  22. Web site: Compendium of Pesticide Common Names: Pydiflumetofen . BCPC . 2023-07-27.
  23. Web site: Chemical Name: Pydiflumetofen US EPA . June 5, 2024 . Pesticide Product and Label System.
  24. Web site: Trebuset - Seed Treatment Product & Label Information Syngenta US . 2024-06-05 . www.syngenta-us.com.

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