Clear Search sequence regions


  • botrytis (1)
  • psoralen (3)
  • psoralen (2)
  • switzerland (1)
  • Sizes of these terms reflect their relevance to your search.

    To search a novel lead structure for antiphytopathogenic fungus agent, a series of novel psoralen derivatives possessing sulfonohydrazide or acylthiourea structure were designed and synthesized, and their fungicidal activity against seven phytopathogens was evaluated. Their structures were confirmed by melting points, 1H NMR, 13C NMR and HRMS, and the typical crystal structure was determined by X-ray diffraction for validation. Preliminary fungicidal activity showed that some of the title compounds exhibited certain-to-high fungicidal activity. Compound I-13 exhibited good fungicidal activity against Botrytis cinerea, Cercospora arachidicola and Physalospora piricola with EC50 values of 12.49, 13.22 and 12.12 μg/mL, respectively. Compounds II-9 and II-15 showed over 90% inhibition against B. cinerea at 50 μg/mL in vitro. In particular, II-9 exhibited significant higher fungicidal activity with a lower EC50 value of 9.09 μg/mL than the positive control YZK-C22 (13.41 μg/mL). Our studies found that sulfonohydrazide or acylthiourea-containing psoralen derivatives were promising fungicide leads deserve for further study. © 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

    Citation

    Jingyue Dong, Kun Li, Zeyu Hong, Lei Chen, Liangfu Tang, Lijun Han, Lai Chen, Zhijin Fan. Design, synthesis and fungicidal evaluation of novel psoralen derivatives containing sulfonohydrazide or acylthiourea moiety. Molecular diversity. 2023 Apr;27(2):571-588

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 35666432

    View Full Text