Novel <i>N</i>‑Phenyltriazinone CarboxylicAcid Derivatives as Promising Protoporphyrinogen IX Oxidase Inhibitors

Protoporphyrinogen IX oxidase (PPO) is a critical target for new herbicide development. We used a scaffold hopping strategy to develop 49 novel <i>N</i>-phenyltriazinone carboxylic acid derivatives and assessed their function as PPO inhibitors. Bioassay revealed that compound <b>D5</b> exhibited excellent inhibitory activity against Nicotiana tabacum PPO (<i>Nt</i>PPO) with a <i>K</i><sub>i</sub> of 33.7 nM, comparable to that of trifludimoxazin (<i>K</i><sub>i</sub> = 31.1 nM). Compound <b>D5</b> also exhibited remarkable postemergence herbicidal activity against five weed species (Setaria faberii, Echinochloa crusgalli, Amaranthus retroflexus, Abutilon juncea, and Portulaca oleracea) at an ultralow concentration (9.375 g a.i./ha), and it showed broad-spectrum herbicidal activity and relatively high safety in wheat, rice, and peanut at 150 and 75 g a.i./ha, respectively. In molecular simulations, compound <b>D5</b> stably binds <i>Nt</i>PPO via π–π stacking with Phe392 and a sandwiched π–alkyl interaction with the key amino acids Leu356 and Leu372. This study shows that the novel <i>N</i>-phenyltriazinone carboxylic acid derivative <b>D5</b> is a promising PPO inhibitor for agricultural weed control.

Publication Details

Journal
Figshare
Published
2025-02-06
DOI
https://doi.org/10.1021/acs.jafc.4c09169.s001
Primary Topic
Weed Control and Herbicide Applications
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article
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article

Novel N‑Phenyltriazinone CarboxylicAcid Derivatives as Promising Protoporphyrinogen IX Oxidase Inhibitors

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Weed Control and Herbicide Applications
article

Novel N‑Phenyltriazinone CarboxylicAcid Derivatives as Promising Protoporphyrinogen IX Oxidase Inhibitors

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Abstract

Protoporphyrinogen IX oxidase (PPO) is a critical target for new herbicide development. We used a scaffold hopping strategy to develop 49 novel <i>N</i>-phenyltriazinone carboxylic acid derivatives and assessed their function as PPO inhibitors. Bioassay revealed that compound <b>D5</b> exhibited excellent inhibitory activity against Nicotiana tabacum PPO (<i>Nt</i>PPO) with a <i>K</i><sub>i</sub> of 33.7 nM, comparable to that of trifludimoxazin (<i>K</i><sub>i</sub> = 31.1 nM). Compound <b>D5</b> also exhibited remarkable postemergence herbicidal activity against five weed species (Setaria faberii, Echinochloa crusgalli, Amaranthus retroflexus, Abutilon juncea, and Portulaca oleracea) at an ultralow concentration (9.375 g a.i./ha), and it showed broad-spectrum herbicidal activity and relatively high safety in wheat, rice, and peanut at 150 and 75 g a.i./ha, respectively. In molecular simulations, compound <b>D5</b> stably binds <i>Nt</i>PPO via π–π stacking with Phe392 and a sandwiched π–alkyl interaction with the key amino acids Leu356 and Leu372. This study shows that the novel <i>N</i>-phenyltriazinone carboxylic acid derivative <b>D5</b> is a promising PPO inhibitor for agricultural weed control.

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