Search Results - "Lümmen, Peter"

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  1. 1

    Geographic spread, genetics and functional characteristics of ryanodine receptor based target-site resistance to diamide insecticides in diamondback moth, Plutella xylostella by Steinbach, Denise, Gutbrod, Oliver, Lümmen, Peter, Matthiesen, Svend, Schorn, Corinna, Nauen, Ralf

    Published in Insect biochemistry and molecular biology (01-08-2015)
    “…Anthranilic diamides and flubendiamide belong to a new chemical class of insecticides acting as conformation sensitive activators of the insect ryanodine…”
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    Journal Article
  2. 2

    Diamide Insecticide Target Site Specificity in the Heliothis and Musca Ryanodine Receptors Relative to Toxicity by Qi, Suzhen, Lümmen, Peter, Nauen, Ralf, Casida, John E

    Published in Journal of agricultural and food chemistry (07-05-2014)
    “…Anthranilic and phthalic diamides act on the ryanodine receptor (RyR), which constitutes the Ca2+-activated Ca2+ channel and can be assayed as shown here in…”
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  3. 3

    Crystallographic investigation of the ubiquinone binding site of respiratory Complex II and its inhibitors by Huang, Li-shar, Lümmen, Peter, Berry, Edward A.

    “…The quinone binding site (Q-site) of Mitochondrial Complex II (succinate-ubiquinone oxidoreductase) is the target for a number of inhibitors useful for…”
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  4. 4

    Three classes of inhibitors share a common binding domain in mitochondrial complex I (NADH:ubiquinone oxidoreductase) by Okun, J.G. (Universitatsklinikum Frankfurt, Germany.), Lummen, P, Brandt, U

    Published in The Journal of biological chemistry (29-01-1999)
    “…We have developed two independent methods to measure equilibrium binding of inhibitors to membrane-bound and partially purified NADH:ubiquinone oxidoreductase…”
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    An intronless tau class glutathione transferase detoxifies several herbicides in flufenacet resistant ryegrass by Dücker, Rebecka, Lümmen, Peter, Wolf, Thomas, Brabetz, Veronika, Beffa, Roland

    Published in Plant physiology (Bethesda) (01-10-2024)
    “…Resistance to pre-emergence herbicides, e.g., inhibitors of the biosynthesis of very-long-chain fatty acids (VLCFAs), is evolving in response to increased use…”
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  9. 9

    The cyclic keto-enol insecticide spirotetramat inhibits insect and spider mite acetyl-CoA carboxylases by interfering with the carboxyltransferase partial reaction by Lümmen, Peter, Khajehali, Jahangir, Luther, Kai, Van Leeuwen, Thomas

    Published in Insect biochemistry and molecular biology (01-12-2014)
    “…Acetyl-CoA carboxylase (ACC) catalyzes the committed and rate-limiting step in fatty acid biosynthesis. The two partial reactions, carboxylation of biotin…”
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  10. 10

    Glutathione transferase plays a major role in flufenacet resistance of ryegrass (Lolium spp.) field populations by Dücker, Rebecka, Zöllner, Peter, Lümmen, Peter, Ries, Susanne, Collavo, Alberto, Beffa, Roland

    Published in Pest management science (01-11-2019)
    “…BACKGROUND Herbicides inhibiting the synthesis of very long‐chain fatty acids (HRAC group K3, WSSA group 15), such as flufenacet, play an important role in…”
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    The novel herbicide icafolin-methyl is a plant-specific inhibitor of tubulin polymerization by Haaf, Klaus-Bernhard, Peters, Olaf, Laber, Bernd, Lange, Gudrun, Gatzweiler, Elmar, Geibel, Sven, Passon, Daniel, Endler, Anne, Lange, Sylvia, Kahlau, Sabine, Eroschenko, Tatjana, Waldraff, Petra, Lümmen, Peter

    Published in Pest management science (19-09-2024)
    “…Without controlling weeds, it is estimated that about one third of global crop yields would be lost. Herbicides remain the most effective solution for weed…”
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    Complex I inhibitors as insecticides and acaricides by Lümmen, Peter

    Published in Biochimica et biophysica acta (06-05-1998)
    “…Structurally diverse synthetic insecticides and acaricides had been shown to inhibit the proton-translocating NADH:ubiquinone oxidoreductase (complex I)…”
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  15. 15

    The design and synthesis of novel inhibitors of NADH:ubiquinone oxidoreductase by Lindell, Stephen D., Ort, Oswald, Lümmen, Peter, Klein, Robert

    Published in Bioorganic & medicinal chemistry letters (19-01-2004)
    “…Potent new inhibitors of NADH:ubiquinone oxidoreductase (complex I) have been designed, with the help of molecular modelling, by hybridisation of known complex…”
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