Discovery of Triazone Derivatives Containing Acylhydrazone and Phenoxypyridine Motifs as Novel Insecticidal and Antiphytopathogenic Fungus Agents
1
College of Architecture and Arts, Taiyuan University of Technology, Jinzhong 030060, China
2
College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, China
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2026, 27(1), 260; https://doi.org/10.3390/ijms27010260
Submission received: 14 November 2025
/
Revised: 17 December 2025
/
Accepted: 18 December 2025
/
Published: 26 December 2025
(This article belongs to the Section Molecular Pharmacology)
Abstract
A series of novel triazone derivatives containing acylhydrazone and phenoxypyridine motifs were designed, synthesized, and evaluated for their biological activities. The bioassay results indicated that most of the target compounds exhibited excellent insecticidal activities against bean aphids. In particular, compounds 3i and 3e showed excellent aphicidal activities comparable to pymetrozine, thus emerging as novel insecticidal lead compounds. Additionally, compounds 3c (60%), 3e (60%), and 3f (60%) exhibited good larvicidal activities against C. pipiens pallens at 0.5 mg/kg. Further fungicidal activity tests revealed that most derivatives exhibited broad-spectrum fungicidal activities. A total of twelve compounds exhibited better fungicidal activities against cercospora arachidicola hori than carbendazim, and eight compounds exhibited better fungicidal activities against fusarium moniliforme than carbendazim. This work suggests that compound 3e could serve as an insecticidal lead compound for further structural optimization.
1. Introduction
Agricultural disasters induced by phytophagous aphids can cause great losses in agricultural production [1]. There are about 100 species of aphids all over the world, which are very difficult to control due to their extremely short life cycle and high reproductive rate [2]. At present, chemical aphicides (carbamates, organophosphorus compounds, and neonicotinoids) remain the primary measure for effectively preventing agricultural disasters. However, widespread and prolonged use of chemical aphicides may lead to resistance and thus become ineffective [3]. Therefore, there is an urgent need to develop novel and efficient green insecticides to control aphids.
Pymetrozine (Figure 1), a triazone insecticide discovered by Syngenta in 1988, exhibited good activities against aphids, white flies, and planthoppers [4]. Since then, such insecticides have attracted great research attention for decades [5,6,7,8,9,10,11]. Our previous studies have also indicated that triazone derivatives containing phenoxypyridine, urea, sulfonamide or sulfonimide, acylhydrazone display significant insecticidal properties [12,13,14,15]. However, only two other commercial insecticides (R-768 and pyrifluquinazon, Figure 1) have been developed so far, the activities of which are significantly lower than that of pymetrozine [16].
Nesterov et al. found that pymetrozine acted on Transient receptor potential channels (TRP channels) [17], which are a super-family of ion channels sensitive to diverse chemical and physical stimuli and which play diverse roles in biology [18]. TRP channels are classified into six subfamilies: TRP canonical, TRP vanilloid, TRP melastatin, TRP ankyrin, TRP polycystin, and TRP mucoliptin [19]. TRPC5 belongs to the canonical subgroup of the TRP super-family. It is a nonselective cation channel that can form many homo- and heterotetrameric channels, which are predominantly expressed in the brain and kidney and can be activated by chemical agents such as compound 1 [20]. Compound 1 is a highly selective, potent TRPC5 antagonist, which may become an important pharmacological tool for research in the pathogenesis of kidney disease [21].
Acylhydrazone plays an important role in pesticide and drug molecular design because of its unique physicochemical properties and outstanding biological activity.
Compound 1, azelastine [22], and compounds 2 and 3 [23] (Figure 2A) containing acylhydrazone moieties are used as TRP antagonists. ABM04, chloridazon, compound 4, and furazolidone (Figure 2B), which contain acylhydrazone moieties, are used as insecticide [24], herbicide [25], fungicide [26], and antituberculosis [27] agents, respectively.
Phenoxypyridine (Figure 2C), the bioisostere of diaryl ethers, has been widely introduced into bioactive molecules and has demonstrated significant biological activities. Chlorfluazuron, diflufenican, fluoxytioconazole, and sorafenib containing phenoxypyridine moieties exhibited insecticidal [28], herbicidal [29], and antifungal [30] activities, respectively.
Based on the above considerations, through the principle of activity splicing, acylhydrazone and phenoxypyridine active moieties were introduced into a triazone core skeleton to synthesize a series of novel triazone derivatives. Their insecticidal and fungicidal activities were evaluated.
2. Results and Discussion
2.1. General Synthesis
The synthetic routes of target compounds 3a–3o are shown in Figure 3. Intermediates 1 and 2 were synthesized according to the literature [12,13]. The condensation of triazinone A and compound B in 1,2-dichloroethane afforded ester C, which reacted with hydrazine hydrate in methanol to yield compound 1. Compounds 3a–3o were synthesized by the condensation of compound 1 and phenoxypyridines 2a–2o under the catalysis of p-toluenesulfonic acid in 22–88% yields. Most target products had high yields; only the yields of compounds 3f, 3g, 3m, and 3o were lower than 50%. 1H NMR, 13C NMR, and HRMS data of compounds 3a–3o are available in the Supplementary Materials.
2.2. Biological Evaluation
2.2.1. Foliar Contact Activity Against Bean Aphid (A. craccivora)
Table 1 shows that most target compounds exhibited good insecticidal activities. Among them, compounds 3b (75%), 3c (70%), 3d (80%), 3e (90%), 3h (70%), 3i (80%) and 3l (75%) still exhibited excellent biological activities at 10 mg/kg. In particular, compounds 3i (80%) and 3e (90%) exhibited the same level of activities as pymetrozine (90%). The activity was moderate compared to literature data [12,13,14,15]. The size of the substituents on the phenoxy group significantly influenced aphicidal activities (3c–3e). For example, an analysis of the structure–activity relationship indicated aphicidal activities in the following order: 3e (p-tert-butyl, 90%) > 3d (p-isopropyl, 80%) > 3c (p-ethyl, 70%). The position of substituents on the phenoxy ring had a significant influence on aphicidal activities; for example, compound 3l (4-isopropyl, 75%) exhibited higher activity than 3m (2-isopropyl, 30%) at 10 mg/kg. At 5mg/kg, the activity of p-tert-butyl substituted compound against Bean Aphids is the highest, followed by p-iodine substituted compound and then p-isopropyl substituted compound. The introduction of electron-withdrawing groups and electron-donating groups will not lead to a significant increase in insecticidal activity.
The rabbit TRPV protein was selected as a homology for molecular docking studies. The target compound was 3e, with pymetrozine serving as the positive control. The protein forms a homotetramer consisting of four subunits (A, B, C, and D). The binding site was defined as the central cavity near the crystallographic ligand Ruthenium Red, a region previously identified in published structures. Within this site, three key residues, Ser542, Thr539 and Asn572, were selected to delineate the binding pocket (Figure 4A).
The results (Figure 4B) show that pymetrozine, due to its smaller size, binds closer to the B and C subunits. Its triazine ring forms a hydrogen bond with Glu522 (subunit C), while also engaging in hydrophobic interactions with Ile541 (B), Asp542 (C), Pro544 (C), and Ala545 (C). In contrast, compound 3e, which incorporates a diaryl group that increases its molecular volume, showed superior complementarity to the binding pocket. The introduced diaryl moiety engages in a π-anion interaction with Asp542 (subunit B). Furthermore, the triazine ring maintains the hydrogen bond with Glu522 (C), while the acyl hydrazone group forms additional hydrogen bonds with Gly543 (C) and Ala545 (C). Compared to pymetrozine, 3e benefits from a greater number of hydrogen bonds and the new π-anion interaction, collectively contributing to stronger target binding. This is corroborated by the molecular docking scores: −7.24 kcal/mol for 3e versus −5.05 kcal/mol for pymetrozine. The enhanced binding affinity provides a structural rationale for the superior insecticidal activity of 3e (Figure 4B).
Based on the molecular docking, it is speculated that the molecule of pymetrozine was relatively small compared to the TRPV5 channel protein binding pocket. This resulted in pymetrozine being unable to effectively bind to the receptor, leading to a low docking score for pymetrozine. Therefore, increasing the molecular volume of molecules and introducing new effective functional groups is key to enhancing the insecticidal activity. By introducing a diaryl fragment, the volume of compound 3e significantly increased. Therefore, compound 3e exhibited insecticidal activity against A. craccivora similar to that of pymetrozine. It also exhibited higher insecticidal activity against C. pipiens pallens than pymetrozine. Subsequent design of compounds can consider introducing large functional groups.
2.2.2. Larvicidal Activities
The larvicidal activities of compounds 3a–3o and pymetrozine against C. pipiens pallens, H. armigera, M. separata, and O. nubilalis are listed in Table 2 and Table 3. The larvicidal activities of compounds 3a, 3c, 3e, and 3f against C. pipiens pallens were higher than that of pymetrozine. Compounds 3c (p-ethyl), 3e (p-tert-butyl), and 3f (p-benzyloxy) showed higher larvicidal activities (60% at 0.5 mg/kg) than that of pymetrozine. Most alkyl substituents exhibited better activities against C. pipiens pallens than other electron withdrawing and electron donating substituents. The larvicidal activity of compound 3a (o-methyl) against H. armigera, O. nubilalis, and M. separata was the highest among the 15 compounds.
2.2.3. Fungicidal Activities
Compounds 3a–3o were also evaluated for their fungicidal activities at 50 mg/kg, with two commercial fungicides, carbendazim and chlorothalonil, used as controls (Table 4). These derivatives showed broad-spectrum fungicidal activities against 14 kinds of plant fungi, with particularly excellent fungicidal activities against Physalospora piricola and Rhizoctonia cerealis. Additionally, all compounds showed better fungicidal activities against Physalospora piricola than carbendazim. Twelve compounds showed better fungicidal activities against Cercospora arachidicola hori than carbendazim, while eight compounds showed better fungicidal activities against Fusarium moniliforme than carbendazim. Compound 3b showed better fungicidal activity against Fusarium graminearum than chlorothalonil and exhibited an inhibition rate greater than 50% against eight kinds of fungi. Compounds 3d, 3g, 3m, and 3n exhibited an inhibition rate greater than 50% against six kinds of fungi.
2.2.4. Toxicity
The acute, mutagenic and carcinogenic toxicities of compounds 3a–3o are listed in Table 5, which were predicted by the Pro Tox-3.0 program. The predicted acute toxicities of compounds 3a–3o are relatively low. The mutagenic and carcinogenic toxicities of compound 3e are negative. Based on the activity and low toxicity of compound 3e, it can be used as a lead compound for further structural optimization.
3. Materials and Methods
Instruments. 1H and 13C NMR spectra were obtained using a Bruker AV400 spectrometer (Bruker Corporation, Billerica, MA, USA) in DMSO-d6, while HRMS data were obtained using an FTICR-MS instrument (Ionspec 7.0 T, Ionspec Corporation, San Diego, CA, USA). The melting points were tested on an X-4 binocular microscope (Beijing Tech Instruments Co., Beijing, China) melting point apparatus.
General synthesis. Pymetrozine was purchased from Chemieliva Pharmaceutical Co. (Chongqing, China) and used as the control in the insecticidal activity tests. Chlorothalonil and carbendazim, which were used in the bactericidal activity tests, were purchased from Bailing Agrochemical Co., Ltd. (Taizhou, China). All reagents were purchased and used directly, and all solvents were dried using standard techniques reported in the literature.
General Procedure for the Preparation of Compounds 3a–3o. To a solution of compound 1 (4.00 mmol) and compounds 2a–2o (4.00 mmol) in methanol (80 mL) was added p-toluene sulfonic acid (0.80 mmol), and then the mixture was refluxed for 6 h. The solution was cooled and then concentrated under reduced pressure. The crude product was purified by flash chromatography on silica gel using petroleum ether (60–90 °C) and ethyl acetate (v/v = 5:1) as eluent to give compound 3a–3o as white solids.
Biological Evaluation. The larvicidal activities of 3a–3o were tested using previously reported methods [31,32,33], while fungicidal activities were tested using a previously reported procedure [34] with pymetrozine as control. The testing process is recorded in detail in the Supplementary Materials.
Molecular docking. Molecular docking was performed using the Molecular Operating Environment (MOE) software (version 2024.06). The molecular docking studies of target compound 3e were conducted with pymetrozine serving as positive control. The rabbit TRPV protein was selected as a homolog for molecular docking studies. The protein crystal structure for molecular docking was selected from the Protein Data Bank (http://www.rcsb.org/) with the PDB ID 8FFN. This structure corresponds to the rabbit TRPV5 channel protein. According to the literature, the crystal contains the ligand ruthenium red, and the binding region of ruthenium red was defined as the protein binding pocket. Based on prior reports, residues Thr539 and Asp542 were identified as key amino acids for ligand binding, and the region surrounding these two residues was selected as the docking site.
Prior to docking, the protein structure was checked and optimized using the Structure Preparation module. The target compounds were energy-minimized using the Amber10:ETH force field. The highest-scoring binding conformation of each compound was used as the initial input. Docking was carried out with the Triangle Matcher placement method at the defined binding site. Semi-flexible docking was conducted using the GBVI/WSA dG scoring function, and 30 docking poses were generated and ranked by score. Finally, cluster analysis was performed using an RMSD threshold of 2.0 Å to select the best-scored pose for each compound. Molecular docking figures were generated using PyMOL v1.8.
Prediction of toxicity Pro Tox-3.0 is a program used to predict acute toxicity, mutagenic toxicity and carcinogenic toxicity of organic compounds, the URL of which is https://tox.charite.de. The prediction results of acute toxicity correspond to rat, oral and range of LD50.
4. Conclusions
In summary, a series of novel triazone derivatives containing acylhydrazone and phenoxypyridine groups were synthesized and evaluated for their insecticidal and fungicidal activities. Compounds 3i and 3e exhibited aphicidal activities comparable to pymetrozine and could be used as lead compounds for further research. According to the results of molecular docking, compound 3e can form more hydrogen bond and π-anion ion interactions with rabbit TRPV protein compared to pymetrozine, which can be confirmed by the molecular docking scores of compound 3e being −7.24 kcal/mol and pymetrozine being −5.05 kcal/mol. The enhanced binding affinity provides a structural rationale for the superior insecticidal activity of 3e.
Compounds 3c, 3e, and 3f exhibited 60% insecticidal activities against C. pipiens pallens at 0.5 mg/Kg. A total of 12 compounds exhibited better fungicidal activities against Cercospora arachidicola hori than carbendazim, and 8 compounds exhibited better fungicidal activities against Fusarium moniliforme than carbendazim. Further studies on these triazone compounds are in progress in our laboratory.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms27010260/s1.
Author Contributions
Data analysis and drafting of manuscript, P.C.; idea conceptualization, compound synthesis, and biological activity testing, Y.Y. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by the National Natural Science Foundation of China, grant numbers 22001190 and 21702144, and the Shanxi Basic Research Program, grant numbers 202303021221016 and 20210302123180.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
The original contributions presented in this study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding authors.
Conflicts of Interest
The authors declare no conflicts of interest.
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Figure 1.
Pymetrozine, R-768, and pyrifluquinazon.
Figure 2.
(A) TRP antagonist. (B) Acylhydrazone unit. (C) Phenoxypyridine unit. (D) Design strategy of target compounds.
Figure 2.
(A) TRP antagonist. (B) Acylhydrazone unit. (C) Phenoxypyridine unit. (D) Design strategy of target compounds.
Figure 3.
Synthesis of compounds 3a–3o.
Figure 4.
(A) The rabbit TRPV protein. (B) Molecular docking diagrams of compound 3e and pymetrozine with the rabbit TRPV protein.
Figure 4.
(A) The rabbit TRPV protein. (B) Molecular docking diagrams of compound 3e and pymetrozine with the rabbit TRPV protein.
Table 1.
Foliar contact activities against A. craccivora of compounds 3a–3o and pymetrozine a.
| Compound |  R | Mortality (%) at Concentration (mg/kg) | |||
|---|---|---|---|---|---|
| 600 | 100 | 10 | 5 | ||
| 3a |  | 100 ± 0 | 100 ± 0 | 40 ± 0 | - |
| 3b |  | 100 ± 0 | 90 ± 0 | 75 ± 2 | 10 ± 0 |
| 3c |  | 100 ± 0 | 95 ± 1 | 70± 0 | 10 ± 0 |
| 3d |  | 100 ± 0 | 100 ± 0 | 80 ± 0 | 15 ± 1 |
| 3e |  | 100 ± 0 | 100 ± 0 | 90 ± 0 | 35 ± 2 |
| 3f |  | 100 ± 0 | 90 ± 0 | 45 ± 2 | - |
| 3g |  | 100 ± 0 | 85 ± 1 | 25 ± 2 | - |
| 3h |  | 100 ± 0 | 100 ± 0 | 70 ± 0 | 10 ± 0 |
| 3i |  | 100 ± 0 | 95 ± 2 | 80 ± 0 | 20 ± 0 |
| 3j |  | 100 ± 0 | 80 ± 0 | 30 ± 0 | - |
| 3k |  | 100 ± 0 | 90 ± 0 | 20 ± 0 | - |
| 3l |  | 100 ± 0 | 95 ± 2 | 75 ± 1 | 10 ± 0 |
| 3m |  | 100 ± 0 | 85 ± 2 | 30 ± 0 | - |
| 3n |  | 100 ± 0 | 80 ± 0 | 20 ± 0 | - |
| 3o |  | 100 ± 0 | 90 ± 0 | 35 ± 2 | - |
| pymetrozine |  | 100 ± 0 | 100 ± 0 | 90 ± 0 | 30 ± 0 |
a Average of three replicates; All results are expressed as mean ± SD; Statistical analysis was conducted using SPSS 27.0 software. Statistical significance was defined as p < 0.05. - Not tested.
Table 2.
Larvicidal activities of compounds 3a–3o and pymetrozine against C. pipiens pallens a.
| Compound | Correcting Mortality (%) at Concentration (mg/kg) | ||||
|---|---|---|---|---|---|
| 10 | 5 | 2 | 1 | 0.5 | |
| 3a | 100 ± 0 | 100 ± 0 | 100 ± 0 | 100 ± 0 | 40 ± 0 |
| 3b | 100 ± 0 | 40 ± 0 | - | - | - |
| 3c | 100 ± 0 | 100 ± 0 | 100 ± 0 | 100 ± 0 | 60 ± 0 |
| 3d | 100 ± 0 | 20 ± 0 | - | - | - |
| 3e | 100 ± 0 | 100 ± 0 | 100 ± 0 | 100 ± 0 | 60 ± 0 |
| 3f | 100 ± 0 | 100 ± 0 | 100 ± 0 | 100 ± 0 | 60 ± 0 |
| 3g | 40 ± 0 | - | - | - | - |
| 3h | 20 ± 0 | - | - | - | - |
| 3i | 100 ± 0 | 30 ± 0 | - | - | - |
| 3j | 100 ± 0 | 30 ± 0 | - | - | - |
| 3k | 100 ± 0 | 100 ± 0 | 60 ± 0 | - | - |
| 3l | 30 ± 0 | - | - | - | - |
| 3m | 100 ± 0 | 100 ± 0 | 60 ± 0 | - | - |
| 3n | 100 ± 0 | 40 ± 0 | - | - | - |
| 3o | 70 ± 0 | - | - | - | - |
| pymetrozine | 100 ± 0 | 40 ± 0 | - | - | - |
a Average of three replicates; All results are expressed as mean ± SD; Statistical analysis was conducted using SPSS 27.0 software. Statistical significance was defined as p < 0.05. - Not tested.
Table 3.
Larvicidal activities of compounds 3a–3o and pymetrozine against H. armigera, O. nubilalis, and M. separata a.
Table 3.
Larvicidal activities of compounds 3a–3o and pymetrozine against H. armigera, O. nubilalis, and M. separata a.
| Compound | Correcting Mortality (%) at Concentration 600 mg/kg | ||
|---|---|---|---|
| H. armigera | O. ubilalis | M. eparata | |
| 3a | 45 ± 2 | 40 ± 0 | 65 ± 1 |
| 3b | 35 ± 1 | 30 ± 0 | 45 ± 2 |
| 3c | 0 | 0 | 5 ± 0 |
| 3d | 20 ± 0 | 10 ± 0 | 20 ± 0 |
| 3e | 15 ± 1 | 10 ± 0 | 20 ± 0 |
| 3f | 0 | 0 | 5 ± 0 |
| 3g | 10 ± 0 | 5 ± 1 | 20 ± 0 |
| 3h | 15 ± 1 | 10 ± 0 | 20 ± 0 |
| 3i | 40 ± 0 | 35 ± 2 | 65 ± 2 |
| 3j | 10 ± 0 | 5 ± 0 | 10 ± 0 |
| 3k | 40 ± 0 | 35 ± 2 | 50 ± 0 |
| 3l | 20 ± 0 | 15 ± 1 | 20 ± 0 |
| 3m | 30 ± 0 | 25 ± 2 | 45 ± 2 |
| 3n | 20 ± 0 | 15 ± 1 | 25 ± 0 |
| 3o | 40 ± 0 | 35 ± 2 | 65 ± 2 |
| pymetrozine | 20 ± 0 | 40 ± 0 | 50 ± 0 |
a Average of three replicates; All results are expressed as mean ± SD; Statistical analysis was conducted using SPSS 27.0 software. Statistical significance was defined as p < 0.05.
Table 4.
In vitro fungicidal activities of compounds 3a–3o, carbendazim, and chlorothalonil against 14 kinds of fungi a.
Table 4.
In vitro fungicidal activities of compounds 3a–3o, carbendazim, and chlorothalonil against 14 kinds of fungi a.
| Compound | Fungicidal Activity (%) a at 50 mg/kg | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AS b | FG | PI | PC | SS | BC | RS | FC | CH | PP | RC | BM | WA | FM | |
| 3a | 18.8 ± 0.6 | 38.5 ± 1.4 | 4.8 ± 2.2 | 24.1 ± 1.9 | 12.1 ± 0.7 | 18.4 ± 0.5 | 10.5 ± 1.8 | 60.0 ± 2.3 | 60.0 ± 0.7 | 80.3 ± 0.9 | 74.1 ± 2.0 | 50.0 ± 1.1 | 39.3 ± 0.9 | 46.7 ± 0.6 |
| 3b | 18.8 ± 1.3 | 57.7 ± 0.5 | 23.8 ± 1.4 | 31.0 ± 0.7 | 20.7 ± 1.3 | 10.5 ± 0.9 | 68.4 ± 1.5 | 52.5 ± 1.8 | 56.0 ± 0.9 | 82.0 ± 1.3 | 80.2 ± 2.6 | 60.0 ± 3.4 | 50.0 ± 1.6 | 63.3 ± 1.7 |
| 3c | 12.5 ± 2.5 | 38.5 ± 1.8 | 9.5 ± 1.9 | 31.0 ± 1.5 | 24.1 ± 1.7 | 13.2 ± 0.5 | 14.0 ± 0.7 | 37.5 ± 1.4 | 52.0 ± 2.1 | 72.1 ± 1.6 | 72.8 ± 2.4 | 47.5 ± 0.6 | 50.0 ± 0.9 | 60.0 ± 2.2 |
| 3d | 12.5 ± 0.8 | 46.2 ± 1.8 | 4.8 ± 1.2 | 27.6 ± 0.9 | 20.7 ± 0.7 | 10.5 ± 0.4 | 22.8 ± 0.5 | 67.5 ± 0.7 | 56.0 ± 0.9 | 73.8 ± 1.6 | 79.0 ± 2.1 | 57.5 ± 2.3 | 53.6 ± 0.9 | 50.0 ± 0.7 |
| 3e | 25.0 ± 1.2 | 11.5 ± 0.9 | 9.5 ± 0.7 | 17.2 ± 0.8 | 24.1 ± 1.3 | 26.3 ± 1.3 | 33.3 ± 1.8 | 47.5 ± 2.2 | 52.0 ± 2.1 | 82.0 ± 0.6 | 80.2 ± 1.2 | 57.5 ± 2.1 | 42.9 ± 1.5 | 60.0 ± 2.4 |
| 3f | 6.3 ± 0.9 | 19.2 ± 0.7 | 4.8 ± 2.1 | 24.1 ± 0.7 | 12.1 ± 0.8 | 10.5 ± 0.5 | 40.4 ± 0.8 | 40.0 ± 2.2 | 44.0 ± 2.6 | 73.8 ± 1.7 | 79.0 ± 1.5 | 60.0 ± 2.7 | 35.7 ± 1.1 | 33.3 ± 0.3 |
| 3g | 6.3 ± 1.1 | 11.5 ± 0.5 | 14.3 ± 0.7 | 10.3 ± 0.9 | 12.1 ± 0.3 | 7.9 ± 0.6 | 10.5 ± 2.6 | 57.5 ± 1.9 | 56.0 ± 0.6 | 83.6 ± 0.9 | 82.7 ± 1.3 | 50.0 ± 1.7 | 57.1 ± 2.1 | 66.7 ± 2.5 |
| 3h | 12.5 ± 1.4 | 30.8 ± 0.5 | 9.5 ± 0.5 | 31.0 ± 1.7 | 20.7 ± 0.7 | 18.4 ± 2.4 | 10.5 ± 1.6 | 35.0 ± 1.2 | 60.0 ± 1.5 | 80.3 ± 2.7 | 82.7 ± 1.9 | 55.0 ± 2.5 | 46.4 ± 1.5 | 50.0 ± 0.8 |
| 3i | 12.5 ± 0.8 | 46.2 ± 2.3 | 9.5 ± 0.9 | 34.5 ± 0.7 | 20.7 ± 1.3 | 10.5 ± 0.5 | 31.6 ± 0.8 | 45.0 ± 1.9 | 56.0 ± 2.5 | 85.2 ± 1.7 | 80.2 ± 2.1 | 62.5 ± 1.2 | 50.0 ± 0.7 | 46.7 ± 0.9 |
| 3j | 12.5 ± 0.8 | 23.1 ± 0.7 | 4.8 ± 0.5 | 6.9 ± 0.9 | 20.7 ± 1.4 | 10.5 ± 1.8 | 14.0 ± 0.5 | 37.5 ± 1.8 | 40.0 ± 0.9 | 55.7 ± 1.4 | 59.3 ± 1.3 | 40.0 ± 1.5 | 35.7 ± 2.2 | 53.3 ± 1.1 |
| 3k | 6.3 ± 0.5 | 19.2 ± 1.4 | 9.5 ± 0.8 | 17.2 ± 0.9 | 15.5 ± 0.7 | 10.5 ± 1.2 | 19.3 ± 0.7 | 35.0 ± 1.5 | 52.0 ± 1.8 | 78.7 ± 2.1 | 77.8 ± 2.6 | 50.0 ± 0.6 | 50.0 ± 1.7 | 56.7 ± 1.3 |
| 3l | 6.3 ± 0.8 | 50.0 ± 3.0 | 4.8 ± 0.5 | 17.2 ± 0.9 | 20.7 ± 0.3 | 18.4 ± 0.5 | 14.0 ± 0.9 | 72.5 ± 3.2 | 36.0 ± 1.2 | 78.7 ± 2.7 | 80.2 ± 1.9 | 47.5 ± 1.5 | 50.0 ± 0.3 | 30.0 ± 0.9 |
| 3m | 12.5 ± 0.5 | 30.8 ± 0.4 | 4.8 ± 0.3 | 20.7 ± 0.7 | 24.1 ± 0.9 | 10.5 ± 1.2 | 36.8 ± 1.0 | 47.5 ± 1.8 | 64.0 ± 3.3 | 77.0 ± 2.4 | 76.5 ± 2.0 | 55.0 ± 1.4 | 53.6 ± 1.6 | 63.3 ± 1.5 |
| 3n | 12.5 ± 0.8 | 46.2 ± 0.7 | 14.3 ± 0.6 | 37.9 ± 0.8 | 20.7 ± 1.6 | 28.9 ± 1.7 | 14.0 ± 0.9 | 47.5 ± 1.2 | 60.0 ± 2.1 | 82.0 ± 0.6 | 80.2 ± 1.8 | 52.5 ± 2.2 | 57.1 ± 0.9 | 70.0 ± 1.3 |
| 3o | 12.5 ± 0.7 | 50.0 ± 1.5 | 23.8 ± 1.0 | 27.6 ± 0.6 | 29.3 ± 0.9 | 10.5 ± 0.6 | 19.3 ± 1.3 | 42.5 ± 1.0 | 52.0 ± 2.3 | 63.9 ± 2.1 | 55.6 ± 2.5 | 35.0 ± 1.3 | 42.9 ± 2.2 | 46.7 ± 1.2 |
| Carbendazim c | <50 | 100 ± 0.0 | 100 ± 0.0 | <50 | 100 ± 0.0 | <50 | 100 ± 0.0 | <50 | <50 | <50 | 100 ± 0.0 | 100 ± 0.0 | 100 ± 0.0 | <50 |
| chlorothalonil c | 73 ± 1 | <50 | 86 ± 1 | 100 ± 0.0 | <50 | 100 ± 0.0 | 100 ± 0.0 | 100 ± 0.0 | 73 ± 1 | 100 ± 0.0 | 100 ± 0.0 | 91 ± 1 | 91 ± 1 | 100 ± 0.0 |
a Average of three replicates; All results are expressed as mean ± SD; Statistical analysis was conducted using SPSS 27.0 software. Statistical significance was defined as p < 0.05. b Abbreviations: AS—Alternaria solani; FG—Fusarium graminearum; PI—Phytophthora infestans; PC—Phytophthora capsici; SS—Sclerotinia sclerotiorum; BC—Botrytis cinerea; RS—Rhizoctonia solani; FC—Fusarium oxysporum f. sp. cucumeris; CH—Cercospora arachidicola Hori; PP—Physalospora piricola; RC—Rhizoctonia cerealis; BM—Bipolaris maydis; WA—watermelon anthracnose; FM—Fusarium moniliforme. c Commercial agricultural fungicides were used to compare antifungal activities.
Table 5.
Predicted toxicity of compounds 3a–3o.
| Compounds | Acut Tox. Pred. (mg/kg) a | Mutigenic Tox. Pred. | Carcinogenic Tox. Pred. |
|---|---|---|---|
| 3a | 75 | negative | negative |
| 3b | 1000 | negative | negative |
| 3c | 75 | negative | positive |
| 3d | 75 | negative | positive |
| 3e | 75 | negative | negative |
| 3f | 75 | negative | positive |
| 3g | 1000 | negative | positive |
| 3h | 75 | negative | negative |
| 3i | 75 | negative | negative |
| 3j | 1000 | positive | positive |
| 3k | 1000 | positive | positive |
| 3l | 200 | negative | negative |
| 3m | 75 | negative | negative |
| 3n | 200 | negative | positive |
| 3o | 75 | negative | negative |
a Rat, oral, LD50.
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MDPI and ACS Style
Cui, P.; Yang, Y. Discovery of Triazone Derivatives Containing Acylhydrazone and Phenoxypyridine Motifs as Novel Insecticidal and Antiphytopathogenic Fungus Agents. Int. J. Mol. Sci. 2026, 27, 260. https://doi.org/10.3390/ijms27010260
AMA Style
Cui P, Yang Y. Discovery of Triazone Derivatives Containing Acylhydrazone and Phenoxypyridine Motifs as Novel Insecticidal and Antiphytopathogenic Fungus Agents. International Journal of Molecular Sciences. 2026; 27(1):260. https://doi.org/10.3390/ijms27010260
Chicago/Turabian StyleCui, Peipei, and Yan Yang. 2026. "Discovery of Triazone Derivatives Containing Acylhydrazone and Phenoxypyridine Motifs as Novel Insecticidal and Antiphytopathogenic Fungus Agents" International Journal of Molecular Sciences 27, no. 1: 260. https://doi.org/10.3390/ijms27010260
APA StyleCui, P., & Yang, Y. (2026). Discovery of Triazone Derivatives Containing Acylhydrazone and Phenoxypyridine Motifs as Novel Insecticidal and Antiphytopathogenic Fungus Agents. International Journal of Molecular Sciences, 27(1), 260. https://doi.org/10.3390/ijms27010260
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