The emergence of multidrug-resistant bacteria and fungi requires the development of
antibiotics and antifungal agents. This review identified natural products isolated from Asian …

Succinate dehydrogenase (SDH) is known as an ideal target for the investigations of
fungicides. To develop novel SDH inhibitors, 30 novel thiophene/furan-1, 3, 4-oxadiazole …

A total of 29 novel quinazoline-2-aminothiazole hybrids containing a 4-piperidinylamide
linker were designed, synthesized, and evaluated for their anti-microbial properties against …

A total of 52 novel 1, 2, 4-triazole thioether and thiazolo [3, 2-b]-1, 2, 4-triazole derivatives
bearing the 6-fluoroquinazolinyl moiety were designed, synthesized, and evaluated as …

Based on the structural features of both succinate dehydrogenase inhibitors (SDHIs) and
targeted covalent inhibitors, a series of N-phenylpropiolamides containing a Michael …

To find potential α-glucosidase inhibitors, thirty-seven cryptolepine derivatives (FM1∼ 37)
were designed and synthesized. Compared to parent compound cryptolepine (IC 50 …

Finding highly active molecular scaffold structures is always the key research content of new
pesticide discovery. In the research and development of new pesticides, the discovery of …

Epidemic diseases of crops caused by fungi deeply affected the course of human history
and processed a major restriction on social and economic development. However, with the …

Based on the structural characteristics of the cryptolepine alkaloid, a series of new
quindoline derivatives bearing various substituents were prepared and evaluated for their …

Although ε-poly-l-lysine (ε-PL) has a good potential as a green fungicide, high concentration
is usually required during its controlling of plant disease. On the other hand, same problems …