4.7 Article

Discovery of Novel Triazolothiadiazines as Fungicidal Leads Targeting Pyruvate Kinase

期刊

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 70, 期 4, 页码 1047-1057

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.1c07022

关键词

pyruvate kinase inhibitor; ring expansion strategy; molecular docking; fungicidal activity

资金

  1. National Natural Science Foundation of China [31872443]
  2. Frontiers Science Center for New Organic Matter, Nankai University [63181206]
  3. National Key Research and Development Program of China [2017YFD0200900]
  4. Tianjin Natural Science Foundation [18JCZDJC33500]
  5. Tianjin Development Program for Innovation and Entrepreneurship
  6. Nature Science Foundation of Beijing, China [7214253]

向作者/读者索取更多资源

Pyruvate kinase (PK) was identified as a potential target for novel fungicides. A series of triazolothiadiazine derivatives were designed and synthesized using a ring expansion strategy and computer-aided pesticide design. Compound 6m showed similar potency to the lead compound YZK-C22 in inhibiting the growth of Rhizoctonia solani, both in vitro and in vivo. Field experiments also demonstrated that 6m had comparable efficacy to thifluzamide against R. solani.
Pyruvate kinase (PK) was discovered as a potent new target for novel fungicide development. A series of novel triazolothiadiazine derivatives were rationally designed and synthesized by a ring expansion strategy and computer-aided pesticide design using the 3D structure of Rhizoctonia solani PK (RsPK) obtained by homology modeling as a receptor and our previously discovered lead YZK-C22 as a ligand. The in vitro bioassay results indicated that compounds 4g, 6h, 6m, 6n, 6o, and 6p exhibited good activity against R. solani with the EC50 values falling between 10.99 and 72.76 mu M. Especially, 6m showed similar potency to YZK-C22 (10.99 vs 11.97 mu M of the EC50 value, respectively). The in vivo bioassay results suggested that 6m against R. solani at a concentration of 200 mu g/mL displayed a numerically higher inhibition than YZK-C22 (70 vs 60%, respectively). A field experiment validated that 6m at an application rate of 120 g ai/ha showed comparable efficacy against R. solani to thifluzamide at an application rate of 80 g ai/ha (77.80 vs 84.5%, respectively). Enzymatic inhibition suggested that the potency of 6m was about twofold lower than that of YZK-C22 (67.30 vs 32.64 mu M of IC50, respectively). Fluorescence quenching studies validated that RsPK was quenched by both 6m and YZK-C22, implying that they both might act at the same target site of PK. A possible binding conformation of 6m in the RsPK active site was depicted by molecular docking. Our studies suggest that 6m could be a fungicidal lead targeting PK.

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