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A Study in Scaffold Hopping: Discovery and Optimization of Thiazolopyridines as Potent Herbicides That Inhibit Acyl-ACP Thioesterase.

Steven A G AbelNeanne AlnaftaElisabeth AsmusBirgit Bollenbach-WahlRalf BraunJan DittgenAnne EndlerJens FrackenpohlJörg FreigangElmar GatzweilerInes HeinemannHendrik HelmkeBernd LaberGudrun LangeAnu MachettiraGillian McArthurThomas MüllerMagdalena OdaybatAnna M ReingruberSina RothChristopher H RosingerDirk SchmutzlerWolfgang SchulteRhea StoppelJörg TiebesGiulio VolpinDavid M Barber
Published in: Journal of agricultural and food chemistry (2023)
In the search for new chemical entities that can control resistant weeds by addressing novel modes of action (MoAs), we were interested in further exploring a compound class that contained a 1,8-naphthyridine core. By leveraging scaffold hopping methodologies, we were able to discover the new thiazolopyridine compound class that act as potent herbicidal molecules. Further biochemical investigations allowed us to identify that the thiazolopyridines inhibit acyl-acyl carrier protein (ACP) thioesterase (FAT), with this being further confirmed via an X-ray cocrystal structure. Greenhouse trials revealed that the thiazolopyridines display excellent control of grass weed species in pre-emergence application coupled with dose response windows that enable partial selectivity in certain crops.
Keyphrases
  • fatty acid
  • tissue engineering
  • adipose tissue
  • small molecule
  • high resolution
  • single cell
  • magnetic resonance imaging
  • risk assessment
  • municipal solid waste
  • anaerobic digestion