《1. Introduction》

1. Introduction

In recent years, the harm caused by soil nematodes has become increasingly serious. In particular, there have been outbreaks of damage from root-knot nematodes in some areas [1,2]. The chemical control agents that are widely available on the market are mainly fosthiazate and avermectin B2a (Fig. 1). Traditional highly toxic or virulent nematicides, such as the carbamates aldicarb, carbofuran, and oxamyl, the organophosphates fenamiphos, cadusafos, fensulfothion, and so forth, have been banned or restricted in China. Early fumigants such as methyl bromide have also been phased out due to the destruction of the ozone layer.

《Fig. 1》

Fig. 1. Chemical structures of fosthiazate and avermectin B2a.

Research on new nematicides is extremely significant in the prevention and control of soil nematodes. At present, nematicidal active ingredients are generally developed by screening existing insecticides, herbicides, or fungicides; however, this process results in the slow development of new nematicides and insufficient control agents for nematodes. Recently, some agrochemical companies have reported several new nematicidal active ingredients (Fig. 2); one of these, fluopyram, is a new amide nematicide that was successfully developed by Bayer AG in Germany and that has also been used as a broad-spectrum fungicide [3–6]. Its mechanism of action is to inhibit succinate dehydrogenase (SDH) in the respiratory electron transport chain of mitochondria [7]. Other nematicidal amide structures have been subsequently reported (Fig. 3) [8–14].

《Fig. 2》

Fig. 2. Recently developed nematicidal active ingredients.

Plant diseases have been recognized as a worldwide threat to crop production, and the use of fungicides has been, is, and will remain critical for the effective control of most plant diseases in agriculture [15]. Among the more than 224 fungicides listed by the Fungicide Resistance Action Committee, the succinate dehydrogenase inhibitor (SDHI) class is the fastest growing in terms of new compounds produced and launched onto the market [16]. Thus far, 23 commercial SDHI fungicides—of which fluopyram possesses a unique amide bridge—have been approved for plant protection since the first launch of carboxin in 1966, and have been extensively applied to combat destructive plant fungi, such as Sclerotinia sclerotiorum, Rhizoctonia solani (RS), and Botrytis cinerea (BC) [17,18].

《Fig. 3》

Fig. 3. Structures of reported nematicidal amide compounds. Het: substituted aromatic heterocycles.

In the present paper, considering that most of the new nematicidal structures reported above have heterocyclic, sulfide, sulfone, and amide substructures [19,20], while the synthetic procedures of fluopyram involve high-temperature deacidification or high-pressure reduction [21], two series of target compounds were designed and synthesized by introducing sulfide, sulfone, and various aromatic rings into the molecular skeleton of fluopyram (Fig. 4) [19,20]. The synthetic routes for the target compounds I-1 to I-12 and II-1 to II-12, and for the intermediate 4a, are displayed in Fig. 5, and have the advantages of convenient synthesis, simple post-processing, and high yield.

《Fig. 4》

Fig. 4. Design strategy of the target compounds. Ar, Ar' : substituted aromatic rings.

《Fig. 5》

Fig. 5. Synthetic route of the target compounds. (a) Organic synthetic route of the target compounds; (b) the structures of different substituted aromatic rings. DMF: N,N-dimethylformamide; mCPBA: meta-chloroperoxybenzoic acid; RT: room temperature; Et: ethyl.

《2. Materials and methods》

2. Materials and methods

《2.1. Reagents and instruments》

2.1. Reagents and instruments

All reaction reagents were of analytical grade. Melting points for target compounds were determined on an X-4 binocular microscope (Gongyi Tech. Instrument Co., China). 1H and 13C nuclear magnetic resonance (NMR) was performed using a Bruker AV400 spectrometer (400 MHz), and chemical-shift values (δ ) were reported as parts per million (ppm) with tetramethylsilane as the internal standard. Mass spectra were recorded using a highresolution mass spectrometer (HRMS) (Varian 7.0 T FTMS, Agilent Technologies, USA). Column chromatography purification was carried out using silica gel (200–300 mesh).

《2.2. Synthesis of target compounds》

2.2. Synthesis of target compounds

The intermediate 3 and 4a and the target compounds I-1 to I-12 and II-1 to II-12 were prepared according to previously reported methods [8,22,23]. The corresponding synthetic procedures and characterization data are available in the Supplementary data.

《2.3. Biological activity screening》

2.3. Biological activity screening

The nematicidal activities of the target compounds against Meloidogyne incognita were screened and evaluated with reference to the literature [24,25]. Eggs of Meloidogyne incognita were extracted from the infected roots of tomato (Solanum lycopersicum L.) into a solution of sodium hypochlorite (NaOCl). To obtain second-stage juveniles (J2), the eggs were spread on a mesh nylon filter (openings 30 μm in diameter) in a Petri dish containing water and incubated at 25 °C. Emerging J2 individuals that passed through the filter were collected daily and used for bioassays immediately. The stock solution was prepared by dissolving the target compounds in dimethyl sulfoxide and diluting with 0.1% Tween-80 aqueous solution. The test solutions were introduced into the wells of 24-well tissue culture plates. In each well, the concentration of nematodes was approximately 100 juveniles of Meloidogyne incognita per 1 mL of water. The plates were covered and maintained at (25 ± 1) °C, and each treatment was replicated three times. Nematode mortality was observed under a stereomicroscope after 24 h. Nematodes were classified as dead if their bodies were motionless (i.e., straight) even after being transferred to clean water for 12 h.

In addition, considering the fungicidal activity of the reference molecule fluopyram, the in vitro fungicidal inhibition rates of the target compounds were investigated using a mycelia growth inhibition method, as previously reported [26]. Common agricultural pathogens, including RS, Gibberella zeae (GZ), Physalospora piricola (PP), Cercospora circumscissa Sacc. (CS), Alternaria kikuchiana Tanaka (AK), BC, Colletotrichum capsici (CC), and Phomopsis vexans (PV), were taken as the test objects.

《2.4. Molecular docking》

2.4. Molecular docking

The Surflex-Dock method [27] was applied to study the binding mode of the target compound I-9, which displayed an excellent fungicidal inhibition rate, with SDH while using the SYBYL 6.9 software package. The literature [7] reports that fluopyram is an SDHI that specifically binds to the ubiquinone-binding site (Q-site) of the mitochondrial SDH. Compound I-9 and fluopyram were manually docked into the active Q-site in Escherichia coli SDH based on the binding positions at the Q-site for ubiquinone in Escherichia coli SDH [28], which were retrieved from the RCSB Protein Data Bank (PDB ID: 1NEK). The receptor and the ligand molecule were prepared using standard procedures.

《3. Results and discussion》

3. Results and discussion

《3.1. Synthetic chemistry》

3.1. Synthetic chemistry

The key intermediate 3 and the target compounds I-1 to I-12 and II-1 to II-12 were designed and synthesized according to the procedures reported in the Supporting data. The acyl chloride 2 was prepared through the chlorination reaction of aromatic formic acid, and then converted to amide 3 by a reaction with 2- chloroethylamine hydrochloride. The aromatic thiophenol 4 was obtained from either the market or laboratory preparation; of these compounds, 3-chloro-5-(trifluoromethyl)pyridine-2-thiol (4a) was synthesized by the nucleophilic substitution of 2,3- dichloro-5-(trifluoromethyl)pyridine and sodium hydrosulfide. Finally, the N-(2-chloroethyl)aromatic amide 3 and thiophenol 4 were reacted to generate the target compounds I-1 to I-12, which were oxidized with meta-chloroperoxybenzoic acid (mCPBA) to yield the products II-1 to II-12. Surprisingly, the sulfur atom on the thiazole ring of compounds I-4, I-8, and I-12 was oxidized to sulfoxide to yield II-4, II-8, and II-12, respectively, under excess mCPBA conditions. The advantages of this result were that the introduction of the sulfide substructure made the synthesis of the target compounds more convenient and faster than that of the control fluopyram, and avoided the reaction conditions of high temperature and high pressure. Subsequently, all target compounds were identified and characterized by 1H NMR, 13C NMR, and HRMS. Several unique structural characteristics were also revealed via the crystal structure of compound I-3 (CCDC Number 1830647, Fig. 6).

《Fig. 6》

Fig. 6. The crystal structure of compound I-3.

《3.2. Biological activity》

3.2. Biological activity

The nematicidal activities of the target compounds against Meloidogyne incognita, with fluopyram as a positive control, are shown in Table 1. According to the data, most compounds displayed excellent nematicidal activity at a concentration of 200 μg·mL-1 , in comparison with fluopyram, except compound I-2. When the test concentration was reduced to 100 μg·mL-1 , the nematicidal activities of the target compounds changed greatly, and most showed lower mortality. However, compounds I-11 and II-6 still exhibited good nematicidal activity at 100 μg·mL-1 , with mortalities of 75% and 70%, respectively, and therefore provide a valuable guide for the further exploration of potential efficient nematicidal lead compounds. In addition, there was little difference in the mortality rates between the sulfide and sulfone substructures.

《Table 1》

Table 1 Nematicidal activity of target compounds against Meloidogyne incognita.

Considering the fungicidal activity of the reference molecule, fluopyram, the fungicidal inhibition rates of the target compounds were further measured. The results are shown in Table 2. According to the data, most of the target compounds showed extremely weak fungicidal activity in comparison with fluopyram, except for compound I-9, whose inhibition rates were almost comparable to those of the control. Furthermore, similar to the nematicidal activity, there was no significant difference in the inhibitory activity between the sulfide and sulfone substructures. Based on the above results, the introduction of sulfide and sulfone substructures and the replacement of the heterocyclic rings had a great influence on the fungicidal activities of the target compounds, perhaps due to the effect of the change in length of the amide bridge in the compounds’ favorable conformations. These results will provide important guidance for subsequent molecular designs of exploring and developing potential fungicidal lead compounds.

《Table 2》

Table 2 Fungicidal activity of target compounds at 100 μg·mL-1 .

To further explore the fungicidal activity of compound I-9, the corresponding half maximal effective concentration (EC50) values of compound I-9 and fluopyram were estimated, and are displayed in Table 3. It can be concluded that compound I-9 and fluopyram have a poor inhibitory effect on Gibberella zeae. Compared with fluopyram, compound I-9 exhibits relatively weak inhibitory activities. However, as a whole, compound I-9 shows excellent fungicidal activity against BC, CC, and PV, compared with other pathogens.

《Table 3》

Table 3 EC50 values of compound I-9 and fluopyram.

《3.3. Molecular docking simulation》

3.3. Molecular docking simulation

The literature [7] reports that the mechanism of action for the fungicidal and nematicidal agent fluopyram involves acting on complex II of the mitochondrial respiratory electron transport chain—namely, SDH or succinate coenzyme Q reductase (SQR). Although the composite crystal structures of fluopyram and the target enzyme SDH have not been reported in the protein database (RCSB PDB), it has been pointed out [28] that amide fungicides acting on SDH specifically bind to the coenzyme Q-site on complex II. Therefore, a careful investigation of the binding pattern of ligands provided a few specific points, which were helpful for correlating in vitro fungicidal data.

The Surflex-Dock method (SYBYL software) was used to simulate the interaction between compound I-9, fluopyram, and Escherichia coli SDH (PDB code: 1NEK), respectively (Fig. 7). From the data, it was concluded that the carbonyl oxygen on the amide and the fluorine atoms on the ortho-trifluoromethyl group of fluopyram facilitated the formation of hydrogen bonds with the amino acid residues B/TRP-164, D/TYR-83, and C/ARG-31 at the Q-site on the target enzyme, which helped to improve the fungicidal activity. Furthermore, the trifluoromethyl group was on the same side of the amide bridge as the carbonyl oxygen, and the two conformed to form hydrogen bonds with the amino acid residue TRP-164 together (Fig. 7(a)).

《Fig. 7》

Fig. 7. (a) The binding mode of fluopyram to Escherichia coli SDH (PDB code: 1NEK); (b) the binding mode of compound I-9 to Escherichia coli SDH; (c) the superposed conformation of fluopyram and compound I-9; (d) the docking pocket of compound I-9 to Escherichia coli SDH, TYP, TRP, ARG, HIS, SER: amino acid residue.

When 3-(difluoromethyl)-1-methyl-1H-pyrazole was introduced into the amide bridge, the presence of the fluorine atoms on the ortho-difluoromethyl group of the amide contributed to the formation of hydrogen bonds with the amino acid residues, which was consistent with the hydrogen bond interaction when using fluopyram. Considering the excellent fungicidal activity and structural characteristics of fluopyram and the target compound I-9, combined with the docking results, it was concluded that the presence of the amide and its ortho-fluorinated groups had an important role in the fungicidal activity. On the other hand, the introduction of different aromatic rings in the aromatic sulfide moiety and the change in the length of the amide bridge had a great influence on the biological activity

《4. Conclusion》

4. Conclusion

In summary, 24 novel target compounds were designed and synthesized by introducing sulfide and sulfone substructures into fluopyram. The bioassays indicated that the structural modification of the target compounds had different effects on the compounds’ nematicidal and fungicidal activities. Although the synthetic routes for the target compounds were optimized through the introduction of sulfide and sulfone, the biological activities were greatly affected. Through the replacement of various heterocycles, compounds I-11 and II-6 with good nematicidal activity and compound I-9 with excellent fungicidal activity were discovered; combined with the molecular docking results, these results provide important guidance for further structural optimization.



This work was financially supported by the Natural Science Foundation of Shandong Province, China (ZR2017BC053), and the Doctoral Research Startup Foundation of Liaocheng University (318051625).

《Compliance with ethics guidelines》

Compliance with ethics guidelines

Xuewen Hua, Nannan Liu, Sha Zhou, Leilei Zhang, Hao Yin, Guiqing Wang, Zhijin Fan, and Yi Ma declare that they have no conflict of interest or financial conflicts to disclose.

《Appendix A. Supplementary data》

Appendix A. Supplementary data

Supplementary data to this article can be found online at https://doi.org/10.1016/j.eng.2019.09.011.