Yu Sun

TL;DR: The results of in vivo antifungal activity of compound 1e against S. sclerotiorum showed that 1e possessed higher curative effects than that of positive control azoxystrobin, which is expected to be a novel leading structure for the development of new antIFungal agents.

TL;DR: The designed assemblage possesses several benefits with a high-profile of variation in synthesized molecules, the ease of synthesis and good cost-effectiveness of commercially available synthetic reagents, all of which have highlighted the potential worth of compound 24 as a new and highly efficient agricultural fungicide.

TL;DR: The optical microscopy and scanning electron microscopy observations revealed that after treating M. oryzae mycelia with sanguinarine, theMycelia appeared curved, collapsed and the cell membrane integrity was eventually damaged, and the membrane function and cell proliferation of mycelIA were destroyed.

TL;DR: The nitrogen atom was inserted into the anthracycline system of the isocryptolepine nucleus to obtain the "Aza"-type structure benzo[4,5]imidazo[1,2-c] quinazoline, which lays the foundation for the future development of isoccryptolepine derivatives as environmentally friendly and safe agricultural fungicides.

TL;DR: In this paper, a series of quinoline compounds containing acylhydrazine and triazole moieties were synthesized and evaluated for their fungicidal activity in vitro and the results indicated that compound 2e displayed superior fungicidal activities and could be a potential fungicidal candidate against plant fungal diseases.