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Russian Chemical Reviews, 1998, Volume 67, Issue 6, Pages 535–544
DOI: https://doi.org/10.1070/RC1998v067n06ABEH000426
(Mi rcr1414)
 

This article is cited in 17 scientific papers (total in 17 papers)

Natural compounds of the strobilurin series and their synthetic analogues as cell respiration inhibitors

V. V. Zakharychev, L. V. Kovalenko

D. Mendeleev University of Chemical Technology of Russia, Moscow
Abstract: A group of fungicidal antibiotics, β-methoxyacrylic acid derivatives (strobilurins, oudemansins, and myxothiazols), their producers, and mechanisms of action are considered. The fungicidal activity of these compounds is based on the suppression of cell respiration of fungi in the bc1-complex of cytochromes. They also manifest other biological activities that are not always coupled with inhibition of respiration. Studies of the structure of the natural methoxyacrylates has made it possible to create a novel class of synthetic agricultural fungicides with enhanced stability, high activity, and a broad spectrum of action. The main regularities of the structure–activity relationship and methods of synthesis of these compounds are discussed. The bibliography includes 159 references.
Received: 10.10.1997
Bibliographic databases:
Document Type: Article
UDC: 577.158.8.04:632.952
Language: English
Original paper language: Russian


Citation: V. V. Zakharychev, L. V. Kovalenko, “Natural compounds of the strobilurin series and their synthetic analogues as cell respiration inhibitors”, Usp. Khim., 67:6 (1998), 595–605; Russian Chem. Reviews, 67:6 (1998), 535–544
Linking options:
  • https://www.mathnet.ru/eng/rcr1414
  • https://doi.org/10.1070/RC1998v067n06ABEH000426
  • https://www.mathnet.ru/eng/rcr/v67/i6/p595
  • This publication is cited in the following 17 articles:
    1. Vladimir V. Zakharychev, Andrey M. Martsynkevich, Advanced Agrochem, 2024  crossref
    2. Valeria Lysakova, Larissa Krasnopolskaya, Maria Yarina, Mayya Ziangirova, Antibiotics, 13:11 (2024), 1026  crossref
    3. Zakharychev V.V. Kuzenkov V A. Martsynkevich A.M., Chem. Heterocycl. Compds., 56:12 (2020), 1491–1516  crossref  isi
    4. Gewehr M., Sauter H., Modern Crop Protection Compounds, Vols 1-3, 3Rd Edition, eds. Jeschke P., Witschel M., Kramer W., Schirmer U., Wiley-V C H Verlag Gmbh, 2019, 634–681  isi
    5. Irina Sidorova, Elena Voronina, Secondary Metabolites of Plant Growth Promoting Rhizomicroorganisms, 2019, 3  crossref
    6. Vorobyev M.M., Kovalenko L.V., Kalistratova A.V., Oshchepkov M.S., Kochetkov K.A., Mammadbeyli E.H., Process. Petrochem. Oil Refin., 18:1 (2017), 18–23  mathscinet  isi
    7. Santi M. Mandal, Anupam Roy, Debarati Paul, Suresh Korpole, Shanker Lal Shrivastava, Ranadhir Chakraborty, Amit Basak, Recent Trends in Antifungal Agents and Antifungal Therapy, 2016, 1  crossref
    8. I. L. Levina, E. A. Fedorova, L. Ya. Kuznetsova, O. A. Zinchuk, Inland Water Biol, 5:2 (2012), 222  crossref
    9. Amal H. Aly, Abdessamad Debbab, Peter Proksch, Fungal Diversity, 50:1 (2011), 3  crossref
    10. Fergus Earley, Hubert Sauter, Joachim Rheinheimer, Heiko Rieck, Pierre‐Yves Coqueron, William G. Whittingham, Harald Walter, Modern Crop Protection Compounds, 2011, 559  crossref
    11. Gerhard Erkel, Industrial Applications, 2011, 123  crossref
    12. Modern Crop Protection Compounds, 2007, 433  crossref
    13. Bernd Schäfer, Naturstoffe der chemischen Industrie, 2006, 467  crossref
    14. L.I. Belen'kii, N.D. Kruchkovskaya, V.N. Gramenitskaya, Advances in Heterocyclic Chemistry, 79, 2001, 199  crossref
    15. V. V. Zakharychev, L. V. Kovalenko, Russ J Electrochem, 36:6 (2000), 914  crossref
    16. V. V. Zakharychev, M. D. Golubtsova, L. V. Kovalenko, Russ Chem Bull, 48:3 (1999), 495  crossref
    17. V. V. ZAKHARYCHEV, L. V. KOVALENKO, ChemInform, 29:52 (1998)  crossref
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