QUANTITATIVE STUDY ON ANTI-PEST ACTIVITY OF NATURAL PRODUCTS BASED ON VISUALIZATION FRAMEWORK OF KNOWLEDGE GRAPH

doi:10.15302/J-FASE-2023488

Frontiers of Agricultural Science and Engineering

, Vol.

Issue (): 0 https://doi.org/10.15302/J-FASE-2023488

本期目录

QUANTITATIVE STUDY ON ANTI-PEST ACTIVITY OF NATURAL PRODUCTS BASED ON VISUALIZATION FRAMEWORK OF KNOWLEDGE GRAPH

Xing LI^1,^2,³, Chunyan GUO^2,^3,⁴, Yumei YAN¹, Lijuan LV⁵, Siqi LI¹, Wenxin GUO¹, Zhengnan LI⁶(

), Minhui LI^1,^2,^3,⁴(

)

¹. College of Pharmacy, Baotou Medical College, Baotou 014040, China
². Inner Mongolia Autonomous Region Hospital of Traditional Chinese Medicine, Hohhot 010110, China
³. Inner Mongolia Academy of Chinese and Mongolian Medicine, Hohhot 010010, China
⁴. College of Pharmacy, Qiqihar Medical University, Qiqihar 161000, China
⁵. Department of Basic Science, Tianjin Agricultural University, Tianjin 300384, China
⁶. Agricultural College, Inner Mongolia Agricultural University, Hohhot 010110, China

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Abstract：

● Using visual analysis to predict the trend of natural product pest resistance.

● Summarized the anti-insect activity and mechanism of natural products.

● Natural compounds insecticide will be the general trend.

To help in the prevention of large-scale loss of agricultural production caused by crop pests, a visual analysis was performed on the main research areas, key countries, organizational cooperation, citation sources and current trends in pest research by searching the literature of Web of Science database and using CiteSpace 5.8.R3 and VOSviewer 1.6.18 software. Additionally, the effects and mechanisms of natural products with anti-insect activity were summarized through visual analysis. According to the bibliometric analysis, keywords such as mortality (232 occurrences), natural enemy (232 occurrences) and spinosad (110 occurrences) were common, and insecticides and natural enemies of pests were the main methods for killing pests. However, pesticide use exhibits numerous limitations. Co-occurring terms in visualization analysis mainly included residue (193 occurrences), detection (153 occurrences), degradation (133 occurrences), recovery (103 occurrences), pyrethroid (97 occurrences) and pesticide residues (65 occurrences). Thus, pesticides cannot fundamentally solve food security; pesticides also pollute the environment and endanger human health. Therefore, green and efficient pesticides that can replace synthetic pesticides are urgently needed. Natural products have recently gained attention in Brazil, China, the USA and other countries because they are green and pollution-free, and new natural pesticides have been developed. This visual analysis combined data mining with literature review and summarize the anti-pest activities and mechanisms of action of natural products. This information provides a foundation and ideas for researchers to study the application and development of natural products in pest control.

Key words： anti-pest activity crop protection insect pest natural product visual analysis

收稿日期: 2022-09-07

Corresponding Author(s): Zhengnan LI,Minhui LI

引用本文:

. [J]. Frontiers of Agricultural Science and Engineering, 10.15302/J-FASE-2023488.
Xing LI, Chunyan GUO, Yumei YAN, Lijuan LV, Siqi LI, Wenxin GUO, Zhengnan LI, Minhui LI. QUANTITATIVE STUDY ON ANTI-PEST ACTIVITY OF NATURAL PRODUCTS BASED ON VISUALIZATION FRAMEWORK OF KNOWLEDGE GRAPH. Front. Agr. Sci. Eng. , , (): 0.

链接本文:

https://academic.hep.com.cn/fase/CN/10.15302/J-FASE-2023488
https://academic.hep.com.cn/fase/CN/Y/V/I/0

Fig.1

Fig.2

Fig.3

Fig.4

Natural product		Compound name	Source	Control target	Insecticidal activity	Positive control	Insecticidal activity	Reference
1	Terpenoids	Azadirachtin	Azadirachta indica A. Juss.	Tirathaba rufivena	LC₅₀ 28.8 mg·L^?1	?	?	[140]
2		Rhodojaponin-III	Rhododendron molle	Spodoptera litura	LC₅₀ 125 μg·mL^?1	Toosendanin	LC₅₀ 250 μg·mL^?1	[116]
3		Laurinterol	Laurencia nidifica	Reticulitermes speratus	LD₅₀ 2.20 μg per insect	Rotenone	LD₅₀ 0.11 μg per insect	[113]
4		Curcuphenol	Didiscus oxeata	Spodopteralittoralis	EC₅₀ 15.8 μg·cm^?2	Thymol	EC₅₀ 23.9 μg·cm^?2	[141]
5		10-Hydroxy-11-methoxy-dihydrocurcuphenol	Didiscus oxeata	Spodopteralittoralis	EC₅₀ 15.8 μg·cm^?2	Thymol	EC₅₀ 23.9 μg·cm^?2	[141]
6		Hydroxycolorenone	Nephthea chabrolii	Spodopteralittoralis	LC₅₀ 8.8 mg·L^?1	?	?	[142]
7		Methoxycolorenone	Nephthea chabrolii	Spodopteralittoralis	LC₅₀ 15.6 mg·L^?1	?	?	[142]
8		Chabrolene	Coral nephthea	Sitophiluszeamais	EC₅₀ 12.5 μg·cm^?2	?	?	[143]
9		3,4-Dihydroxybenzoic acid	Holothuria atra	Spodopteralitura	LC₅₀ 6.01 mg·mL^?1	?	?	[144]
10		4-Hydroxy-3-methoxy-benzaldehyde	Holothuria atra	Spodopteralitura	LC₅₀ 17.01 mg·mL^?1	?	?	[144]
11		Sporyzin A	Aspergillus oryzae	Artemia salina	61.9% mortality at 100 mg·L^?1	Huperzine A	98% mortality	[145]
12		Sporyzin B			42.9% mortality at 100 mg·L^?1
13		Sporyzin C			32.8% mortality at 100 mg·L^?1
14		JBIR-03			74.2% mortality at 100 mg·L^?1
15		Emindole SB			60.3% mortality at 100 mg·L^?1
16		Emeniveol			31.4% mortality at 100 mg·L^?1
17	Alkaloids	Coclaurine	Discaria chacaye	Drosophila melanogaster	LD₅₀ 78.2 μg·mL^?1	?	?	[146]
18		Boldine	Talguenea quinquenervia		LD₅₀ 70.8 μg·mL^?1	?	?
19		Pukateine	Peumus boldus		LD₅₀ 70.9 μg·mL^?1	?	?
20		Sophocarpine	Sophora alopecuroides	ACP	50 mg·mL^?1	N,N-Diethyl-meta-toluamide	30 mg·mL^?1	[83]
21		Sophoridine	Sophora alopecuroides	ACP	70 mg·mL^?1	N,N-Diethyl-meta-toluamide	30 mg·mL^?1	[83]
22		Curviflorain A	Corydalis curviflora Maxim.	Culex pipiens pallens, Aedes albopictus	LC₅₀ 15.9 μg·mL^?1, LC₅₀ 8.42 μg·mL^?1	Pyrethrin	LC₅₀ 4.36 μg·mL^?1, LC₅₀ 3.54 μg·mL^?1	[82]
23		Curviflorain B			LC₅₀ 16.1 μg·mL^?1, LC₅₀ 15.5 μg·mL^?1
24		Ambiguanine A			LC₅₀ 50.1 μg·mL^?1, LC₅₀ 86.0 μg·mL^?1
25		1,1-Dimethyl-6-methoxy-7-hydroxyl-1,2,3,4-tetrahydroisoquinoline			LC₅₀ 52.1 μg·mL^?1, LC₅₀ 76.9 μg·mL^?1
26		Hendersine B			LC₅₀ 23.3 μg·mL^?1, LC₅₀ 31.0 μg·mL^?1
27		Coryximine			LC₅₀ 54.29 μg·mL^?1, LC₅₀ 94.3 μg·mL^?1
28		Isochotensine			LC₅₀ 92.4 μg·mL^?1, LC₅₀ 99.8 μg·mL^?1
29		Bruceine D	Brucea Javanica (L.) Merr.	Plutella xylostella, Spodoptera exigua Hübner, Spodoptera litura Fabricius	Antifeedant effects 93.8%	Azadirachtin	Antifeedant effects 22.6%	[84]
30		Anisodine	Anisodus tanguticus (Maxim.) Pascher	Brevicoryne brassicae	LC₅₀ 3.16 mg·mL^?1	Rotenone	LC₅₀ 0.400 mg·mL^?1	[147]
31				Rhopalosiphum padi	LC₅₀ 3.67 mg·mL^?1		LC₅₀ 1.18 mg·mL^?1
32				Myzus persicae	LC₅₀ 4.16 mg·mL^?1		LC₅₀ 0.566 mg·mL^?1
33				Aphis craccivora	LC₅₀ 0.495 mg·mL^?1		LC₅₀ 0.617 mg·mL^?1
34				Aphis gossypii	LC₅₀ 0.429 mg·mL^?1		LC₅₀ 0.436mg·mL^?1
35				Sitobion miscanthi	LC₅₀ 0.881 mg·mL^?1		LC₅₀ 1.03 mg·mL^?1
36		Anisodamine		Brevicoryne brassicae	LC₅₀ 1.32 mg·mL^?1		LC₅₀ 0.400 mg·mL^?1
37				Rhopalosiphum padi	LC₅₀ 1.64 mg·mL^?1		LC₅₀ 1.18 mg·mL^?1
38				Myzus persicae	LC₅₀ 0.846 mg·mL^?1		LC₅₀ 0.566 mg·mL^?1
39				Aphis craccivora	LC₅₀ 1.95 mg·mL^?1		LC₅₀ 0.617 mg·mL^?1
40				Aphis gossypii	LC₅₀ 0.404 mg·mL^?1		LC₅₀ 0.436 mg·mL^?1
41				Sitobion miscanthi	LC₅₀ 1.164 mg·mL^?1		LC₅₀ 1.030 mg·mL^?1
42		Aloperine	Sophora alopecuroides	Bursaphelenchus xylophilus	Inhibition of reproduction 100%	?	?	[148]
43		Caulerpin	Caulerpa racemosa	Culex pipiens	LC₅₀ 0.86 mg·L^?1	Malathion	LC₅₀ 1.00 mg·L^?1	[149]
44		Caulerpinic acid	Caulerpa racemosa	Culex pipiens	LC₅₀ 1.69 mg·L^?1	Malathion	LC₅₀ 1.00 mg·L^?1	[149]
45		Hymenialdisine	Axinella carteri	Spodopteralittoralis	LD₅₀ 88 mg·L^?1	Precocene II	LD₅₀ 275 mg·L^?1	[150]
46		Debromohymenialdisine	Axinella carteri	Spodopteralittoralis	LD₅₀ 125 mg·L^?1	Precocene II	LD₅₀ 275 mg·L^?1	[150]
47		Manzamine A	Xestospongia ashmorica	Spodopteralittoralis	ED₅₀ 35 mg·L^?1	?	?	[151]
48		Amphitoxin	Amphimedoncompressa	Cylasformicarius	30% mortality at 1.2 mg·L^?1	?	?	[152]
49		Gelastatin A	Cymbastela sp.	Spodopteraexigua	LC₅₀ 20.3 mg·L^?1	Javelin WG	LC₅₀ 12 mg·L^?1	[153]
50		Gelastatin C	Cymbastela sp.	Spodopteraexigua	LC₅₀ 200 mg·L^?1	Javelin WG	LC₅₀ 12 mg·L^?1	[153]
51		Swinhoeiamide A	Theonella swinhoei	Spodopteralittoralis	LC₅₀ 2.98 mg·L^?1	?	?	[154]
52		Nortopsentin A	Spongosoritesruetzleri	Culex pipiens pallens	100% mortality at 10 mg·L^?1	Rotenone	100% mortality	[155]
53		Nortopsentin B			100% mortality at 10 mg·L^?1
54		Nortopsentin C			70% mortality at 10 mg·L^?1
55		Nortopsentin D			40% mortality at 10 mg·L^?1
56		Altemicidin	Streptomycessioyaensis	Artemia salina	LC₅₀ 3 mg·L^?1	Polynactin	LC₅₀ 4 mg·L^?1	[115]
57		Communesin B	Penicillium sp.	Bombyx mori	LD₅₀ 5 μg·g^?1	?	?	[156]
58		Communesin E	Penicillium sp.	Bombyx mori	LD₅₀ 80 μg·g^?1	?	?	[156]
59		Cristatumin B	Eurotium cristatum EN220	Artemia salina	LD₅₀ 74.4 μg·g^?1	?	?	[157]
60		Isoechinulin A			LD₅₀ 16.9 μg·g^?1	?	?
61		Variecolorin G			LD₅₀ 42.6 μg·g^?1	?	?
62		Cyclopentanepropanoic acid, 3,5-bis(acetyloxy)-2-(3-(methoxyimino)octyl),methyl ester	Streptomyces-VITSTK7 sp.	Culexquinquefasciatus	LC₅₀ 430.06 mg·L^?1	?	?	[158]
63		5-Azidomethyl-3-(2-ethoxycarbonyl-ethyl)-4-ethoxycarbo-nylmethyl-1H-pyrrole-2-carboxylic acid,ethyl ester	Streptomyces-VITSTK7 sp.	Culexquinquefasciatus	LC₅₀ 881.59 mg·L^?1	?	?	[158]
64		Chloramphenicol D1	Acremoniumvitellinum	Helicoverpaarmigera	LC₅₀ 930 mg·L^?1	Matrine	LC₅₀ 240 mg·L^?1	[159]
65		Chloramphenicol D2			LC₅₀ 560 mg·L^?1
66		Chloramphenicol D3			LC₅₀ 910 mg·L^?1
67		Okalaminei B	Aspergillus sp.	Spodopteraexigua	LD₅₀ 0.2 μg·g^?1	?	?	[160]
68	Flavonoids	Rotenone	Derris trifoliata Lour.	Derris trifoliata Lour.	LC₅₀ 9.51 mg·L^?1	?	?	[102]
69		Quercetin dihydrate	Rice	Eriosoma lanigerum	Mortality at 85.00%	Imidacloprid	Mortality at 88.3%	[103]
70		Naringin			Mortality at 86.7%
71		Rutin hydrate			Mortality at 93.3%
72		Neochamaejasmine A	Stellera chamaejasme	Aphidoidea	Rate of population decline 74.1%	Imidacloprid	Rate of population decline 71.1%	[104]
73		Quercetin	Hypericum ascyron	Calliptamus abbreviatus	Survival rate 42.3%	?	?	[140]
74	Others	Curcumin	Curcuma longa	Tetranychus cinnabarinus Boisduval	LC₅₀ 3060 mg·L^?1	Spirodiclofen	LC₅₀ 661 mg·L^?1	[161]
75		Matrine	Sophora flavescens		EC₅₀ 238 μg·mL^?1
76		Emodin	Cassia nigricans	Anopheles gambiaea	LC₈₅ 50 μg·mL^?1	?	?	[162]
77		Emodin	Cassia nigricans	Bemisia tabaci	LC₈₅ 25 μg·mL^?1	?	?	[162]
78		Penicixanthenes A	Ceriops tagal	Culex quinquefasciatus	LC₅₀ 38.5 μg·mL^?1	Azadirachtin	LC₅₀ 8.8 μg·mL^?1	[163]
79		Penicixanthenes B			LC₅₀ 80 μg·mL^?1
80		Penicixanthenes C			LC₅₀ 11.6 μg·mL^?1
81		Penicixanthenes D			LC₅₀ 23.5 μg·mL^?1

Tab.1

Fig.5

1	M, Ghorbanpour M, Omidvari P, Abbaszadeh-Dahaji R, Omidvar K Kariman . Mechanisms underlying the protective effects of beneficial fungi against plant diseases. Biological Control, 2018, 117: 147–157 https://doi.org/10.1016/j.biocontrol.2017.11.006
2	T J, Bruce L J, Wadhams C M Woodcock . Insect host location: a volatile situation. Trends in Plant Science, 2005, 10(6): 269–274 https://doi.org/10.1016/j.tplants.2005.04.003 pmid: 15949760
3	G, Lengai J W, Muthomi E R Mbega . Phytochemical activity and role of botanical pesticides in pest management for sustainable agricultural crop production. Scientific American, 2020, 7: e00239 https://doi.org/10.1016/j.sciaf.2019.e00239
4	S, Kumar G, Bhanjana A, Sharma M C, Sidhu N Dilbaghi . Synthesis, characterization and on field evaluation of pesticide loaded sodium alginate nanoparticles. Carbohydrate Polymers, 2014, 101(3): 1061–1067 https://doi.org/10.1016/j.carbpol.2013.10.025 pmid: 24299874
5	H M, Tahir T, Basheer S, Ali R, Yaqoob S, Naseem S Y Khan . Effect of pesticides on biological control potential of neoscona theisi (Araneae: Araneidae). Journal of Insect Science, 2019, 19(2): 17–22 https://doi.org/10.1093/jisesa/iez024 pmid: 30915446
6	R, Kodešová M, Kočárek V, Kodeš O, Drábek J, Kozák K Hejtmánková . Pesticide adsorption in relation to soil properties and soil type distribution in regional scale. Journal of Hazardous Materials, 2011, 186(1): 540–550 https://doi.org/10.1016/j.jhazmat.2010.11.040 pmid: 21144657
7	Y, Liang M C, Guo C, Fan H Q, Dong G L, Ding W B, Zhang G, Tang J L, Yang D D, Kong Y S Cao . Development of novel urease-responsive pendimethalin microcapsules using silica-IPTS-PEI as controlled release carrier materials. ACS Sustainable Chemistry & Engineering, 2017, 5(6): 4802–4810 https://doi.org/10.1021/acssuschemeng.7b00208
8	Y M Luo . Natural Medicinal Chemistry. Wuhan: Huazhong University of Science and Technology, 2011 (in Chinese)
9	A H, Mossa S M M, Mohafrash N Chandrasekaran . Safety of natural insecticides: toxic effects on experimental animals. BioMed Research International, 2018, 2018(10): 4308054 https://doi.org/10.1155/2018/4308054 pmid: 30410930
10	J, He Z Q, Ma X Zhang . Review of botanical pesticide. Journal of Northwest A & F University (Natural Science Edition), 2006, (9): 79−85 (in Chinese)
11	G, Benelli R, Pavela C, Giordani L, Casettari G, Curzi L, Cappellacci R, Petrelli F Maggi . Acute and sub-lethal toxicity of eight essential oils of commercial interest against the filariasis mosquito Culex quinquefasciatus and the housefly Musca domestica. Industrial Crops and Products, 2018, 112: 668−680
12	H, Qu M, Lv X, Yu X, Lian H Xu . Discovery of some piperine-based phenylsulfonylhydrazone derivatives as potent botanically narcotic agents. Scientific Reports, 2015, 5(1): 13077 https://doi.org/10.1038/srep13077 pmid: 26268805
13	R, Rizzo Verde G, Lo M, Sinacori F, Maggi L, Cappellacci R, Petrelli S, Vittori M R, Morshedloo N G B Y, Fofie G Benelli . Developing green insecticides to manage olive fruit flies? Ingestion toxicity of four essential oils in protein baits on Bactrocera oleae. Industrial Crops and Products, 2020, 143: 111884
14	G, Shi Z, Kang F, Ren Y, Zhou P Guo . Effects of quercetin on the growth and expression of immune-pathway-related genes in silkworm (Lepidoptera: Bombycidae). Journal of Insect Science, 2020, 20(6): ieaa124 https://doi.org/10.1093/jisesa/ieaa124 pmid: 33159528
15	N G, Kavallieratos M C, Boukouvala N, Ntalli A, Skourti E S, Karagianni E P, Nika D C, Kontodimas L, Cappellacci R, Petrelli K, Cianfaglione M R, Morshedloo L A, Tapondjou R, Rakotosaona F, Maggi G Benelli . Effectiveness of eight essential oils against two key stored-product beetles, Prostephanus truncatus (Horn) and Trogoderma granarium Everts. Food and Chemical Toxicology: an International Journal Published for the British Industrial Biological Research Association, 2020, 139: 111255 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/32165233 pmid: 32165233
16	R, Bibi R M, Tariq M Rasheed . Toxic assessment, growth disrupting and neurotoxic effects of red seaweeds’ botanicals against the dengue vector mosquito Aedes aegypti L. Ecotoxicology and Environmental Safety, 2020, 195: 110451 https://doi.org/10.1016/j.ecoenv.2020.110451 pmid: 32199214
17	G, Mao Y, Tian Z, Sun J, Ou H Xu . Bruceine D isolated from Brucea Javanica (L.) Merr. as a systemic feeding deterrent for three major Lepidopteran pests. Journal of Agricultural and Food Chemistry, 2019, 67(15): 4232–4239 https://doi.org/10.1021/acs.jafc.8b06511 pmid: 30901209
18	M H, Na C F, Li J, Ting C H, Zhang Z G, Yang M H Li . Research progress of botanical pesticide resources in Inner Mongolia. Modern Chinese medicine, 2017, 19(7): 907–916, 933 (in Chinese)
19	M, Gallo A, Formato D, Ianniello A, Andolf E, Conte M, Ciaravolo V, Varchetta D Naviglio . Supercritical fluid extraction of pyrethrins from pyrethrum flowers (Chrysanthemum cinerariifolium) compared to traditional maceration and cyclic pressurization extraction. Journal of Supercritical Fluids, 2017, 119: 104–112 https://doi.org/10.1016/j.supflu.2016.09.012
20	M, Reges E M, Marinho M M Marinho . Theoretical study of the natural insecticide rotenone clitoriacetal. International Journal of Recent Research and Review, 2019, 12(4): 1–5
21	R C, Bernardes W F, Barbosa G F, Martins M A P Lima . The reduced-risk insecticide azadirachtin poses a toxicological hazard to stingless bee Partamona helleri (Friese, 1900) queens. Chemosphere, 2018, 201: 550–556 https://doi.org/10.1016/j.chemosphere.2018.03.030 pmid: 29533804
22	M, Bajda A, Łoś M Merska . Effect of amphotericin B on the biochemical markers in the haemolymph of honey bees. Medycyna Weterynaryjna, 2014, 70(12): 766–769
23	Y P, Jing H, An S, Zhang N, Wang S Zhou . Protein kinase C mediates juvenile hormone-dependent phosphorylation of Na+/K+-ATPase to induce ovarian follicular patency for yolk protein uptake. Journal of Biological Chemistry, 2018, 293(52): 20112–20122 https://doi.org/10.1074/jbc.RA118.005692 pmid: 30385509
24	C C, Sheeja V V, Thushara L Divya . Caste-specific expression of Na+/K+-ATPase in the Asian weaver ant, Oecophylla smaragdina (Fabricius, 1775). Neotropical Entomology, 2018, 47(6): 763–768 https://doi.org/10.1007/s13744-018-0598-3 pmid: 29572631
25	R Feyereisen . Origin and evolution of the CYP4G subfamily in insects, cytochrome P450 enzymes involved in cuticular hydrocarbon synthesis. Molecular Phylogenetics and Evolution, 2020, 143: 106695 https://doi.org/10.1016/j.ympev.2019.106695 pmid: 31805344
26	T W, Harrop S, Denecke Y T, Yang J, Chan P J, Daborn T, Perry P Batterham . Evidence for activation of nitenpyram by a mitochondrial cytochrome P450 in Drosophila melanogaster. Pest Management Science, 2018, 74(7): 1616–1622 https://doi.org/10.1002/ps.4852 pmid: 29316188
27	L S, Bai C X, Zhao J J, Xu C, Feng Y Q, Li Y L, Dong Z Q Ma . Identification and biochemical characterization of carboxylesterase 001G associated with insecticide detoxification in Helicoverpa armigera. Pesticide Biochemistry and Physiology, 2019, 157: 69–79
28	B, Tang Y, Cheng Y, Li W, Li Y, Ma Q, Zhou K Lu . Adipokinetic hormone enhances CarE-mediated chlorpyrifos resistance in the brown planthopper. Nilaparvata lugens. Insect Molecular Biology, 2020, 29(6): 511–522 https://doi.org/10.1111/imb.12659 pmid: 32686884
29	J H, Cho K M, Lee Y I, Lee H G, Nam W B Jeon . Glutamate decarboxylase 67 contributes to compensatory insulin secretion in aged pancreatic islets. Islets, 2019, 11(2): 33–43 https://doi.org/10.1080/19382014.2019.1599708 pmid: 31084527
30	G, Liu H, Li J, Shi W, Wang K, Furuta D, Liu C, Zhao F, Ozoe X, Ju Y Ozoe . 4-Aryl-5-carbamoyl-3-isoxazolols as competitive antagonists of insect GABA receptors: synthesis, biological activity, and molecular docking studies. Bioorganic & Medicinal Chemistry, 2019, 27(2): 416–424 https://doi.org/10.1016/j.bmc.2018.12.018 pmid: 30579800
31	G, Romano N, Holodkov R, Klima F, Grilli C, Guarnaccia M, Nizzardo F, Rizzo R, Garcia F Feiguin . Downregulation of glutamic acid decarboxylase in Drosophila TDP-43-null brains provokes paralysis by affecting the organization of the neuromuscular synapses. Scientific Reports, 2018, 8(1): 1809 https://doi.org/10.1038/s41598-018-19802-3 pmid: 29379112
32	J Y, Zhang Q, Han Z Y, Jing H L, Li M F, Deng K, Zhu M J, Li H X Duan . Chitinase inhibitors and synthesis and agricultural bioactivity of thiazolidinones: a review. Chinese Journal of Pesticide Science, 2021, 23(3): 1−22 (in Chinese)
33	S, Caveney B C Donly . Neurotransmitter transporters in the insect nervous system. Advances in Insect Physiology, 2002, 29(2): 55–149 https://doi.org/10.1016/S0065-2806(02)29002-5
34	J A, Bigner S E, Fiester J W, Fulcher C M G, Schammel M E, Ward H E, Burney J F, Wheeler S K, Wheeler J M Teuber . Glyphosate and polyoxyethyleneamine ingestion leading to renal, hepatic, and pulmonary failure. American Journal of Forensic Medicine and Pathology, 2021, 42(3): 282–285 https://doi.org/10.1097/PAF.0000000000000660 pmid: 33491949
35	Y, Kamijo M, Takai T Sakamoto . A multicenter retrospective survey of poisoning after ingestion of herbicides containing glyphosate potassium salt or other glyphosate salts in Japan. Clinical Toxicology, 2016, 54(2): 147–151 https://doi.org/10.3109/15563650.2015.1121271 pmid: 26691886
36	J, Langrand I, Blanc-Brisset D, Boucaud-Maitre E, Puskarczyk P, Nisse R, Garnier C Pulce . Increased severity associated with tallowamine in acute glyphosate poisoning. Clinical Toxicology, 2020, 58(3): 201–203 https://doi.org/10.1080/15563650.2019.1623406 pmid: 31169038
37	Z, Che X, Guo Y, Li S, Zhang L, Zhu J, He D, Sun Y, Guo Y, Liu R, Wei X, Huang S, Liu G, Chen Y Tian . Synthesis of paeonol ester derivatives and their insecticidal, nematicidal, and anti-oomycete activities. Pest Management Science, 2022, 78(8): 3442–3455 https://doi.org/10.1002/ps.6985 pmid: 35567371
38	D, Li Z, Li W, Chen X Yang . Imaging and detection of carboxylesterase in living cells and zebrafish pretreated with pesticides by a new near-infrared fluorescence off-on probe. Journal of Agricultural and Food Chemistry, 2017, 65(20): 4209–4215 https://doi.org/10.1021/acs.jafc.7b00959 pmid: 28475833
39	T R, Bilbo D R, Owens J R, Golec J F Walgenbach . Impact of insecticide programs on pests, the predatory mite Phytoseiulus persimilis, and staked tomato profitability. Pest Management Science, 2022, 78(6): 2390–2397 https://doi.org/10.1002/ps.6866 pmid: 35277921
40	S J, Yu L, Cong Q, Pan L L, Ding S, Lei L Y, Cheng Y H, Fang Z T, Wei H Q, Liu C Ran . Whole genome sequencing and bulked segregant analysis suggest a new mechanism of amitraz resistance in the citrus red mite, Panonychus citri (Acari: Tetranychidae). Pest Management Science, 2021, 77(11): 5032–5048 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/34223705 pmid: 34223705
41	C, Bu B, Peng Y, Cao X, Wang Q, Chen J, Li G Shi . Novel and selective acetylcholinesterase inhibitors for Tetranychus cinnabarinus (Acari: Tetranychidae). Insect Biochemistry and Molecular Biology, 2015, 66: 129–135 https://doi.org/10.1016/j.ibmb.2015.10.012 pmid: 26520174
42	G A, Mueller L C, Pedersen J, Glesner L L, Edwards J, Zakzuk R E, London L K, Arruda M D, Chapman L, Caraballo A Pomés . Analysis of glutathione S-transferase allergen cross-reactivity in a North American population: relevance for molecular diagnosis. Journal of Allergy and Clinical Immunology, 2015, 136(5): 1369–1377 https://doi.org/10.1016/j.jaci.2015.03.015 pmid: 25930195
43	J, Carnés V, Iraola S H, Cho R E Esch . Mite allergen extracts and clinical practice. Annals of Allergy, Asthma & Immunology: Official Publication of the American College of Allergy, Asthma & Immunology, 2017, 118(3): 249–256
44	I B, Stanaway J C, Wallace A, Shojaie W C, Griffith S, Hong C S, Wilder F H, Green J, Tsai M, Knight T, Workman E M, Vigoren J S, McLean B, Thompson E M Faustman . Human oral buccal microbiomes are associated with farmworker status and azinphos-methyl agricultural pesticide exposure. Applied and Environmental Microbiology, 2016, 83(2): e02149-16 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/27836847 pmid: 27836847
45	M E, Moriarty T W, Vickers D L, Clifford D K, Garcelon P M, Gaffney K W, Lee J L, King C L, Duncan W M Boyce . Ear mite removal in the Santa Catalina Island fox (Urocyon littoralis catalinae): controlling risk factors for cancer development. PLoS One, 2015, 10(12): e0144271 https://doi.org/10.1371/journal.pone.0144271 pmid: 26641820
46	H, Abdel-Gawad F, Mahdy A, Hashad G H Elgemeie . Fate of 14C-ethion insecticide in the presence of deltamethrin and dimilin pesticides in cotton seeds and oils, removal of ethion residues in oils, and bioavailability of its bound residues to experimental animals. Journal of Agricultural and Food Chemistry, 2014, 62(51): 12287–12293 https://doi.org/10.1021/jf504010h pmid: 25420216
47	J B, Knaak C C, Dary X, Zhang R W, Gerlach R, Tornero-Velez D T, Chang R, Goldsmith J N Blancato . Parameters for pyrethroid insecticide QSAR and PBPK/PD models for human risk assessment. Reviews of Environmental Contamination and Toxicology, 2012, 219: 1–114 pmid: 22610175
48	Q, Lu Y, Sun I, Ares A, Anadón M, Martínez M R, Martínez-Larrañaga Z, Yuan X, Wang M A Martínez . Deltamethrin toxicity: a review of oxidative stress and metabolism. Environmental Research, 2019, 170: 260–281 https://doi.org/10.1016/j.envres.2018.12.045 pmid: 30599291
49	X, Wang M A, Martínez M, Dai D, Chen I, Ares A, Romero V, Castellano M, Martínez J L, Rodríguez M R, Martínez-Larrañaga A, Anadón Z Yuan . Permethrin-induced oxidative stress and toxicity and metabolism. A review. Environmental Research, 2016, 149: 86–104 https://doi.org/10.1016/j.envres.2016.05.003 pmid: 27183507
50	M G, Zoh J M, Bonneville J, Tutagata F, Laporte B K, Fodjo C S, Mouhamadou C G, Sadia J, McBeath F, Schmitt S, Horstmann S, Reynaud J P David . Experimental evolution supports the potential of neonicotinoid-pyrethroid combination for managing insecticide resistance in malaria vectors. Scientific Reports, 2021, 11(1): 19501 https://doi.org/10.1038/s41598-021-99061-x pmid: 34593941
51	X, Tu W Chen . Overview of analytical methods for the determination of neonicotinoid pesticides in honeybee products and honeybee. Critical Reviews in Analytical Chemistry, 2021, 51(4): 329–338 https://doi.org/10.1080/10408347.2020.1728516 pmid: 32072823
52	T, Luo X, Wang Y Jin . Low concentrations of imidacloprid exposure induced gut toxicity in adult zebrafish (Danio rerio). Comparative Biochemistry and Physiology, Toxicology & Pharmacology: CBP, 2021, 241: 108972 https://doi.org/10.1016/j.cbpc.2020.108972 pmid: 33418081
53	J L, Maino A, Cushen R, Valavi P A Umina . Spatial variation in Australian neonicotinoid usage and priorities for resistance monitoring. Journal of Economic Entomology, 2021, 114(6): 2524–2533 https://doi.org/10.1093/jee/toab192 pmid: 34871446
54	C, Negro Pérez-Cejuela H, Martínez E F, Simó-Alfonso J M, Herrero-Martínez R, Bruno D, Armentano J, Ferrando-Soria E Pardo . Highly efficient removal of neonicotinoid insecticides by thioether-based (multivariate) metal-organic frameworks. ACS Applied Materials & Interfaces, 2021, 13(24): 28424–28432 https://doi.org/10.1021/acsami.1c08833 pmid: 34121386
55	A J, Crossthwaite S, Rendine M, Stenta R Slater . Target-site resistance to neonicotinoids. Journal of Chemical Biology, 2014, 7(4): 125–128 https://doi.org/10.1007/s12154-014-0116-y pmid: 25320645
56	E M, Peterson F B, Green P N Smith . Toxic responses of blue orchard mason bees (Osmia lignaria) following contact exposure to neonicotinoids, macrocyclic lactones, and pyrethroids. Ecotoxicology and Environmental Safety, 2021, 208: 111681 https://doi.org/10.1016/j.ecoenv.2020.111681 pmid: 33396013
57	H A, Khan W, Akram S A Shad . Genetics, cross-resistance and mechanism of resistance to spinosad in a field strain of Musca domestica L. (Diptera: Muscidae). Acta Tropica, 2014, 130: 148–154 https://doi.org/10.1016/j.actatropica.2013.11.006 pmid: 24262668
58	N, Abbas H, Khan S A Shad . Cross-resistance, stability, and fitness cost of resistance to imidacloprid in Musca domestica L., (Diptera: Muscidae). Parasitology Research, 2015, 114(1): 247–255 https://doi.org/10.1007/s00436-014-4186-0 pmid: 25342464
59	Júnior E, Ferrari Santos J B A, Dos E D Caldas . Drugs, pesticides and metabolites in forensic post-mortem blood samples. Medicine, Science, and the Law, 2021, 61(2): 97–104 https://doi.org/10.1177/0025802420965006 pmid: 33081562
60	N N, Karpun E B, Yanushevskaya Y V, Mikhailova J, Díaz-Torrijo Y A, Krutyakov A A, Gusev A Neaman . Side effects of traditional pesticides on soil microbial respiration in orchards on the Russian Black Sea coast. Chemosphere, 2021, 275: 130040 https://doi.org/10.1016/j.chemosphere.2021.130040 pmid: 33647685
61	C J, Beringer K W, Goyne R N, Lerch E B, Webb D Mengel . Clothianidin decomposition in Missouri wetland soils. Journal of Environmental Quality, 2021, 50(1): 241–251 https://doi.org/10.1002/jeq2.20175 pmid: 33169408
62	M, Tudi Ruan H, Daniel L, Wang J, Lyu R, Sadler D, Connell C, Chu D T Phung . Agriculture development, pesticide application and its impact on the environment. International Journal of Environmental Research and Public Health, 2021, 18(3): 1112 https://doi.org/10.3390/ijerph18031112 pmid: 33513796
63	M, Lazarus Lovaković B, Tariba T, Orct A, Sekovanić N, Bilandžić M, Đokić Kolanović B, Solomun I, Varenina A, Jurič Lugomer M, Denžić D Bubalo . Difference in pesticides, trace metal(loid)s and drug residues between certified organic and conventional honeys from Croatia. Chemosphere, 2021, 266: 128954 https://doi.org/10.1016/j.chemosphere.2020.128954 pmid: 33250227
64	X S, He Y L, Zhang Z H, Liu D, Wei G, Liang H T, Liu B D, Xi Z B, Huang Y, Ma B S Xing . Interaction and coexistence characteristics of dissolved organic matter with toxic metals and pesticides in shallow groundwater. Environmental Pollution, 2020, 258: 113736 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/31877467 pmid: 31877467
65	K, Hage-Ahmed K, Rosner S Steinkellner . Arbuscular mycorrhizal fungi and their response to pesticides. Pest Management Science, 2019, 75(3): 583–590 https://doi.org/10.1002/ps.5220 pmid: 30255557
66	J, Riedo F E, Wettstein A, Rösch C, Herzog S, Banerjee L, Büchi R, Charles D, Wächter F, Martin-Laurent T D, Bucheli F, Walder der Heijden M G A van . Widespread occurrence of pesticides in organically managed agricultural soils-the ghost of a conventional agricultural past. Environmental Science & Technology, 2021, 55(5): 2919–2928 https://doi.org/10.1021/acs.est.0c06405 pmid: 33534554
67	J, Riedo C, Herzog S, Banerjee K, Fenner F, Walder der Heijden M G A, van T D Bucheli . Concerted evaluation of pesticides in soils of extensive grassland sites and organic and conventional vegetable fields facilitates the identification of major input processes. Environmental Science & Technology, 2022, 56(19): 13686–13695 https://doi.org/10.1021/acs.est.2c02413 pmid: 36099238
68	G, Romanazzi V, Mancini R, Foglia D, Marcolini M, Kavari S Piancatelli . Use of chitosan and other natural compounds alone or in different strategies with copper hydroxide for control of grapevine downy mildew. Plant Disease, 2021, 105(10): 3261–3268 https://doi.org/10.1094/PDIS-06-20-1268-RE pmid: 33206016
69	P M, Guarda A M S, Pontes R S, Domiciano L D S, Gualberto D B, Mendes E A, Guarda Silva J E C da . Assessment of ecological risk and environmental behavior of pesticides in environmental compartments of the Formoso River in Tocantins, Brazil. Archives of Environmental Contamination and Toxicology, 2020, 79(4): 524–536 https://doi.org/10.1007/s00244-020-00770-7 pmid: 33150460
70	N, Zhang L, Huang Y, Zhang L, Liu C, Sun X Lin . Sulfur deficiency exacerbates phytotoxicity and residues of imidacloprid through suppression of thiol-dependent detoxification in lettuce seedlings. Environmental Pollution, 2021, 291: 118221 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/34740294 pmid: 34740294
71	H, Zhao Y, Wang M, Guo Y, Liu H, Yu M Xing . Environmentally relevant concentration of cypermethrin or/and sulfamethoxazole induce neurotoxicity of grass carp: involvement of blood-brain barrier, oxidative stress and apoptosis. Science of the Total Environment, 2021, 762: 143054 https://doi.org/10.1016/j.scitotenv.2020.143054 pmid: 33127128
72	C, Song J, Yang M, Zhang G, Ding C, Jia J, Qin L Guo . Marine natural products: the important resource of biological insecticide. Chemistry & Biodiversity, 2021, 18(5): e2001020 https://doi.org/10.1002/cbdv.202001020 pmid: 33855815
73	A, Khursheed M A, Rather V, Jain A R, Wani S, Rasool R, Nazir N A, Malik S A Majid . Plant based natural products as potential ecofriendly and safer biopesticides: a comprehensive overview of their advantages over conventional pesticides, limitations and regulatory aspects. Microbial Pathogenesis, 2022, 173(Pt A): 105854
74	B C, Gerwick T C Sparks . Natural products for pest control: an analysis of their role, value and future. Pest Management Science, 2014, 70(8): 1169–1185 https://doi.org/10.1002/ps.3744 pmid: 24478254
75	M I, Christodoulou J, Tchoumtchoua A L, Skaltsounis A, Scorilas M Halabalaki . Natural alkaloids intervening the insulin pathway: new hopes for anti-diabetic agents. Current Medicinal Chemistry, 2019, 26(32): 5982–6015 https://doi.org/10.2174/0929867325666180430152618 pmid: 29714135
76	C, Liu S, Yang K, Wang X, Bao Y, Liu S, Zhou H, Liu Y, Qiu T, Wang H Yu . Alkaloids from traditional Chinese medicine against hepatocellular carcinoma. Biomedicine & Pharmacotherapy, 2019, 120: 109543 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/31655311 pmid: 31655311
77	S B, Symington A, Zhang W, Karstens Houten J, Van Clark J Marshall . Characterization of pyrethroid action on ciliary calcium channels in paramecium tetraurelia. Pesticide Biochemistry and Physiology, 1999, 65(3): 181–193 https://doi.org/10.1006/pest.1999.2444
78	A T, Coimbra S, Ferreira A P Duarte . Genus Ruta: a natural source of high value products with biological and pharmacological properties. Journal of Ethnopharmacology, 2020, 260: 113076 https://doi.org/10.1016/j.jep.2020.113076 pmid: 32534112
79	W, Gao J, Guo L, Xie C, Peng L, He X, Wan R Hou . Washing fresh tea leaves before picking decreases pesticide residues in tea. Journal of the Science of Food and Agriculture, 2020, 100(13): 4921–4929 https://doi.org/10.1002/jsfa.10553 pmid: 32472940
80	T, Manimegalai K, Raguvaran M, Kalpana R Maheswaran . Green synthesis of silver nanoparticle using Leonotis nepetifolia and their toxicity against vector mosquitoes of Aedes aegypti and Culex quinquefasciatus and agricultural pests of Spodoptera litura and Helicoverpa armigera. Environmental Science and Pollution Research International, 2020, 27(34): 43103–43116
81	M, Tudi Ruan H, Daniel L, Wang J, Lyu R, Sadler D, Connell C, Chu D T Phung . Agriculture development, pesticide application and its impact on the environment. International Journal of Environmental Research and Public Health, 2021, 18(3): 1112 https://doi.org/10.3390/ijerph18031112 pmid: 33513796
82	J, Xia Y, Liu Y, Zhou J, Zhang C, Li X, Yin X, Tian X Zhang . Two novel alkaloids from Corydalis curviflora Maxim. and their insecticidal activity. Pest Management Science, 2020, 76(7): 2360–2367 https://doi.org/10.1002/ps.5772 pmid: 32020760
83	S A H, Rizvi S, Ling F, Tian J, Liu X Zeng . Interference mechanism of Sophora alopecuroides L. alkaloids extract on host finding and selection of the Asian citrus psyllid Diaphorina citri Kuwayama (Hemiptera: Psyllidae). Environmental Science and Pollution Research International, 2019, 26(2): 1548–1557 https://doi.org/10.1007/s11356-018-3733-0 pmid: 30430450
84	T, Ma X, Shi S, Ma Z, Ma X Zhang . Evaluation of physiological and biochemical effects of two Sophora alopecuroides alkaloids on pea aphids Acyrthosiphon pisum. Pest Management Science, 2020, 76(12): 4000–4008
85	T Y, Wang Q, Li K S Bi . Bioactive flavonoids in medicinal plants: structure, activity and biological fate. Asian Journal of Pharmaceutical Sciences, 2018, 13(1): 12–23 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/32104374 pmid: 32104374
86	S J, Maleki J F, Crespo B Cabanillas . Anti-inflammatory effects of flavonoids. Food Chemistry, 2019, 299: 125124 https://doi.org/10.1016/j.foodchem.2019.125124 pmid: 31288163
87	R, Kaur K, Kaur R, Arora B, Saini S Arora . Natural fused heterocyclic flavonoids: potent candidates as anti-inflammatory and anti-allergic agents in the treatment of asthma. Current Bioactive Compounds, 2021, 17(1): 28–40 https://doi.org/10.2174/1573407215666191120125608
88	D, Raffa B, Maggio M V, Raimondi F, Plescia G Daidone . Recent discoveries of anticancer flavonoids. European Journal of Medicinal Chemistry, 2017, 142: 213–228 https://doi.org/10.1016/j.ejmech.2017.07.034 pmid: 28793973
89	Y, Wang Y, Gao H, Ding S, Liu X, Han J, Gui D Liu . Subcritical ethanol extraction of flavonoids from Moringa oleifera leaf and evaluation of antioxidant activity. Food Chemistry, 2017, 218: 152–158 https://doi.org/10.1016/j.foodchem.2016.09.058 pmid: 27719892
90	T Y, Chou M J, Yang S K, Tseng S S, Lee C C Chang . Tea silkworm droppings as an enriched source of tea flavonoids. Journal of Food and Drug Analysis, 2018, 26(1): 41–46 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/29389582 pmid: 29389582
91	M, Li X, Gao M, Lan X, Liao F, Su L, Fan Y, Zhao X, Hao G, Wu X Ding . Inhibitory activities of flavonoids from Eupatorium adenophorum against acetylcholinesterase. Pesticide Biochemistry and Physiology, 2020, 170: 104701 https://doi.org/10.1016/j.pestbp.2020.104701 pmid: 32980054
92	W T, Hay R W, Behle M A, Berhow A C, Miller G W Selling . Biopesticide synergy when combining plant flavonoids and entomopathogenic baculovirus. Scientific Reports, 2020, 10(1): 6806 https://doi.org/10.1038/s41598-020-63746-6 pmid: 32321975
93	P L D, Silva G, Cordeiro C R D, Silva R A, Barros C R D, Silva J C, Zanuncio W G, Campos M G A Oliveira . Does mechanical damage on soybean induces the production of flavonoids. Anais da Academia Brasileira de Ciências, 2018, 90(4): 3415–3422 https://doi.org/10.1590/0001-3765201820170850 pmid: 30365711
94	N, Devrnja I, Kostić J, Lazarević J, Savić D Ćalić . Evaluation of tansy essential oil as a potential “green” alternative for gypsy moth control. Environmental Science and Pollution Research International, 2020, 27(11): 11958–11967 https://doi.org/10.1007/s11356-020-07825-1 pmid: 31983003
95	L H, Jin B A, Song S, Yang D Y Hu . The recent progress of natural product as plant virucides. Agrochemicals, 2003, 42(4): 10−12 (in Chinese)
96	Z X, Hu J B, Zou Q, An P, Yi C M, Yuan W, Gu L J, Huang H Y, Lou L H, Zhao X J Hao . Anti-tobacco mosaic virus (TMV) activity of chemical constituents from the seeds of Sophora tonkinensis. Journal of Asian Natural Products Research, 2021, 23(7): 644–651
97	J Y, Zeng T M, Vuong J H, Shi Z B, Shi J X, Guo G C, Zhang B Bi . Avermectin stress varied structure and function of gut microbial community in Lymantria dispar asiatica (Lepidoptera: Lymantriidae) larvae. Pesticide Biochemistry and Physiology, 2020, 164: 196–202 https://doi.org/10.1016/j.pestbp.2020.01.013 pmid: 32284127
98	G, Zhang H, Zou N, Geng N, Ding Y, Wang J, Zhang C Zou . Fenoxycarb and methoxyfenozide (RH-2485) affected development and chitin synthesis through disturbing glycometabolism in Lymantria dispar larvae. Pesticide Biochemistry and Physiology, 2020, 163: 64–75 https://doi.org/10.1016/j.pestbp.2019.10.009 pmid: 31973871
99	M, Bisbal M, Remedi G, Quassollo A, Cáceres M Sanchez . Rotenone inhibits axonogenesis via an Lfc/RhoA/ROCK pathway in cultured hippocampal neurons. Journal of Neurochemistry, 2018, 146(5): 570–584 https://doi.org/10.1111/jnc.14547 pmid: 29972689
100	K, Lu Y, Cheng Y, Li W, Li R, Zeng Y Song . Phytochemical flavone confers broad-spectrum tolerance to insecticides in Spodoptera litura by activating ROS/CncC-mediated xenobiotic detoxification pathways. Journal of Agricultural and Food Chemistry, 2021, 69(26): 7429–7445 https://doi.org/10.1021/acs.jafc.1c02695 pmid: 34169724
101	J L, Rodríguez-Chávez V, Egas E, Linares R, Bye T, Hernández F J, Espinosa-García G Delgado . Mexican Arnica (Heterotheca inuloides Cass. Asteraceae: Astereae): ethnomedical uses, chemical constituents and biological properties. Journal of Ethnopharmacology, 2017, 195: 39–63 https://doi.org/10.1016/j.jep.2016.11.021 pmid: 27847336
102	R R, Wen L, Ma W Y, Dong B Y Wang . Toxic effect of rotenone on gypsy moth. Journal of Northeast Forestry University, 2016, 44(9): 103–105, 111 (in Chinese)
103	A, Mazen A R, Saeid A D Mohmmad . Impact of flavonoids against woolly apple aphid, Eriosoma lanigerum (Hausmann) and its sole parasitoid, Aphelinus mali (Hald.). Journal of Agricultural Science, 2012, 4(2): 227–236
104	L W, Song X H, Zhang H M Shen . Comparison of different actions of 1.6% daphneantoxin EW on four vegetable pest. Plant Protection, 2017, 43(1): 218−223 (in Chinese)
105	A, Konarska B Łotocka . Glandular trichomes of Robinia viscosa Vent. var. hartwigii (Koehne) Ashe (Faboideae, Fabaceae)-morphology, histochemistry and ultrastructure. Planta, 2020, 252(6): 102 https://doi.org/10.1007/s00425-020-03513-z pmid: 33180181
106	D Tholl . Biosynthesis and biological functions of terpenoids in plants. Advances in Biochemical Engineering/Biotechnology, 2015, 148: 63–106 https://doi.org/10.1007/10_2014_295 pmid: 25583224
107	J Grassmann . Terpenoids as plant antioxidants. Vitamins and Hormones, 2005, 72: 505–535 https://doi.org/10.1016/S0083-6729(05)72015-X pmid: 16492481
108	S B, Ateba M A, Mvondo S T, Ngeu J, Tchoumtchoua C F, Awounfack D, Njamen L Krenn . Natural terpenoids against female breast cancer: a 5-year recent research. Current Medicinal Chemistry, 2018, 25(27): 3162–3213 https://doi.org/10.2174/0929867325666180214110932 pmid: 29446727
109	A, Ahmad R K, Tiwari I A Ansari . Revisiting the antiviral efficacy of terpenoids: plausible adjunct therapeutics for novel SARS-CoV-2. Endocrine, Metabolic & Immune Disorders Drug Targets, 2021, 21(12): 2119–2130 https://doi.org/10.2174/1871530321666210520102042 pmid: 34061008
110	S A, Zacchino E, Butassi M D, Liberto M, Raimondi A, Postigo M Sortino . Plant phenolics and terpenoids as adjuvants of antibacterial and antifungal drugs. Phytomedicine, 2017, 37: 27–48 https://doi.org/10.1016/j.phymed.2017.10.018 pmid: 29174958
111	D Tholl . Biosynthesis and biological functions of terpenoids in plants. Advances in Biochemical Engineering/Biotechnology, 2015, 148: 63–106 https://doi.org/10.1007/10_2014_295 pmid: 25583224
112	I, Arberas-Jiménez S, García-Davis A, Rizo-Liendo I, Sifaoui M, Reyes-Batlle O, Chiboub R L, Rodríguez-Expósito A R, Díaz-Marrero J E, Piñero J J, Fernández J Lorenzo-Morales . Laurinterol from Laurencia johnstonii eliminates Naegleria fowleri triggering PCD by inhibition of ATPases. Scientific Reports, 2020, 10(1): 17731 https://doi.org/10.1038/s41598-020-74729-y pmid: 33082417
113	T, Ishii T, Nagamine B Nguyen . Insecticidal and repellent activities of laurinterol from the okinawan red alga Laurencia nidifica. Records of Natural Products, 2017, 11(1): 63–68
114	Q, Jia H, Zeng J, Zhang S, Gao N, Xiao J, Tang X, Dong W Xie . The crystal structure of the Spodoptera litura chemosensory protein CSP8. Insects, 2021, 12(7): 602 https://doi.org/10.3390/insects12070602 pmid: 34357261
115	C G, Webster H, Park A F, Ennis J Hong . Synthetic efforts toward the bicyclo[3.2.1]octane fragment of rhodojaponin III. Tetrahedron Letters, 2021, 71: 153055 https://doi.org/10.1016/j.tetlet.2021.153055 pmid: 34054153
116	D M, Cheng Z X, Zhang M Y Hu . Study on the control effect of the crude extract of rhododendron molle and rhodojaponin-III to the larvae of Spodoptera litura larvae. Journal of Changjiang Vegetables, 2007, 4(5): 47−49 (in Chinese)
117	K A, Neelam A, Khatkar K K Sharma . Phenylpropanoids and its derivatives: biological activities and its role in food, pharmaceutical and cosmetic industries. Critical Reviews in Food Science and Nutrition, 2020, 60(16): 2655–2675 https://doi.org/10.1080/10408398.2019.1653822 pmid: 31456411
118	A, Devi V K, Das D Deka . Evaluation of the eectiveness of potato peel extract as a natural antioxidanton biodiesel oxidation stability. Industrial Crops and Products, 2018, 123: 454–460 https://doi.org/10.1016/j.indcrop.2018.07.022
119	G U, Seong I W, Hwang S K Chung . Antioxidant capacities and polyphenolics of Chinese cabbage (Brassica rapa L. ssp. Pekinensis) leaves. Food Chemistry, 2016, 199: 612–618 https://doi.org/10.1016/j.foodchem.2015.12.066 pmid: 26776015
120	A, Hematpoor S Y, Liew M S, Azirun K Awang . Insecticidal activity and the mechanism of action of three phenylpropanoids isolated from the roots of Piper sarmentosum Roxb. Scientific Reports, 2017, 7(1): 12576 https://doi.org/10.1038/s41598-017-12898-z pmid: 28974710
121	A, Pengsook A, Puangsomchit T, Yooboon V, Bullangpoti W Pluempanupat . Insecticidal activity of isolated phenylpropanoids from Alpinia galanga rhizomes against Spodoptera litura. Natural Product Research, 2021, 35(23): 5261–5265
122	J H, Yi H, Perumalsamy K, Sankarapandian B R, Choi Y J Ahn . Fumigant toxicity of phenylpropanoids identified in Asarum sieboldii aerial parts to Lycoriella ingenua (Diptera: Sciaridae) and Coboldia fuscipes (Diptera: Scatopsidae). Journal of Economic Entomology, 2015, 108(3): 1208–1214 https://doi.org/10.1093/jee/tov064 pmid: 26470247
123	T, Xiaorong H Taiping . Separation and identification of botanical insecticide 7-hydroxycoumarin and its biological activity against Aphis craccivora and Culex pipiens pallens. Natural Product Research, 2008, 22(4): 365–370 https://doi.org/10.1080/14786410701856009 pmid: 18322853
124	M, Maleck P O, Hollanda M T, Serdeiro R O, Soares N A, Honório C G Silva . Toxicity and larvicidal activity of podophyllum-based lignans against Aedes aegypti (Diptera: Culicidae). Journal of Medical Entomology, 2017, 54(1): 159–166 https://doi.org/10.1093/jme/tjw130 pmid: 28082643
125	C, Niculaes A, Abramov L, Hannemann M Frey . Plant protection by benzoxazinoids—Recent insights into biosynthesis and function. Agronomy, 2018, 8(8): 143 https://doi.org/10.3390/agronomy8080143
126	J M, Mwendwa P A, Weston J D, Weidenhamer I S, Fomsgaard H, Wu S, Gurusinghe L A Weston . Metabolic profiling of benzoxazinoids in the roots and rhizosphere of commercial winter wheat genotypes. Plant and Soil, 2021, 466(1−2): 467−489
127	Y, Wang X Y, Mei Y X, Liu F, Du M, Yang Y Q Zu . Research progress of benzoxazinoids as defense related substances in plants. Journal of Plant Physiology, 2021, 57(4): 767−779 (in Chinese)
128	F C, Wouters B, Blanchette J, Gershenzon D G Vassão . Plant defense and herbivore counter-defense: benzoxazinoids and insect herbivores. Phytochemistry Reviews : Proceedings of the Phytochemical Society of Europe, 2016, 15(6): 1127–1151 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/27932939 pmid: 27932939
129	S, Ahmad N, Veyrat R, Gordon-Weeks Y, Zhang J, Martin L, Smart G, Glauser M, Erb V, Flors M, Frey J Ton . Benzoxazinoid metabolites regulate innate immunity against aphids and fungi in maize. Plant Physiology, 2011, 157(1): 317–327 https://doi.org/10.1104/pp.111.180224 pmid: 21730199
130	G, Glauser G, Marti N, Villard G A, Doyen J L, Wolfender T C, Turlings M Erb . Induction and detoxification of maize 1,4-benzoxazin-3-ones by insect herbivores. The Plant Journal: for Cell and Molecular Biology, 2011, 68(5): 901–911 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/21838747 pmid: 21838747
131	L N, Meihls V, Handrick G, Glauser H, Barbier H, Kaur M M, Haribal A E, Lipka J, Gershenzon E S, Buckler M, Erb T G, Köllner G Jander . Natural variation in maize aphid resistance is associated with 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one glucoside methyltransferase activity. Plant Cell, 2013, 25(6): 2341–2355 https://doi.org/10.1105/tpc.113.112409 pmid: 23898034
132	Z S, Batyrshina B, Yaakov R, Shavit A, Singh V Tzin . Comparative transcriptomic and metabolic analysis of wild and domesticated wheat genotypes reveals differences in chemical and physical defense responses against aphids. BMC Plant Biology, 2020, 20(1): 19 https://doi.org/10.1186/s12870-019-2214-z pmid: 31931716
133	J, Guo J, Guo K, He S, Bai T, Zhang J, Zhao Z Wang . Physiological responses induced by Ostrinia furnacalis (Lepidoptera: Crambidae) feeding in maize and their effects on O. furnacalis performance. Journal of Economic Entomology, 2017, 110(2): 739–747 https://doi.org/10.1093/jee/tox060 pmid: 28334193
134	V, Handrick C A, Robert K R, Ahern S, Zhou R A, Machado D, Maag G, Glauser F E, Fernandez-Penny J N, Chandran E, Rodgers-Melnik B, Schneider E S, Buckler W, Boland J, Gershenzon G, Jander M, Erb T G Köllner . Biosynthesis of 8-O-methylated benzoxazinoid defense compounds in maize. Plant Cell, 2016, 28(7): 1682–1700 https://doi.org/10.1105/tpc.16.00065 pmid: 27317675
135	C, Zhang J, Li S, Li C, Ma H, Liu L, Wang J, Qi J Wu . ZmMPK6 and ethylene signalling negatively regulate the accumulation of anti-insect metabolites DIMBOA and DIMBOA-Glc in maize inbred line A188. New Phytologist, 2021, 229(4): 2273–2287 https://doi.org/10.1111/nph.16974 pmid: 32996127
136	D, Maag C, Dalvit D, Thevenet A, Köhler F C, Wouters D G, Vassão J, Gershenzon J L, Wolfender T C J, Turlings M, Erb G Glauser . 3-β-D-Glucopyranosyl-6-methoxy-2-benzoxazolinone (MBOA-N-Glc) is an insect detoxification product of maize 1,4-benzoxazin-3-ones. Phytochemistry, 2014, 102: 97–105 https://doi.org/10.1016/j.phytochem.2014.03.018 pmid: 24713572
137	A, Kulmatiski K H, Beard J R, Stevens S M Cobbold . Plant-soil feedbacks: a meta-analytical review. Ecology Letters, 2008, 11(9): 980–992 https://doi.org/10.1111/j.1461-0248.2008.01209.x pmid: 18522641
138	S, Cadot V, Gfeller L, Hu N, Singh A, Sánchez-Vallet G, Glauser D, Croll M, Erb der Heijden M G A, van K Schlaeppi . Soil composition and plant genotype determine benzoxazinoid-mediated plant-soil feedbacks in cereals. Plant, Cell & Environment, 2021, 44(12): 3502–3514 https://doi.org/10.1111/pce.14184 pmid: 34505297
139	L, Hu C A M, Robert S, Cadot X, Zhang M, Ye B, Li D, Manzo N, Chervet T, Steinger der Heijden M G A, van K, Schlaeppi M Erb . Root exudate metabolites drive plant-soil feedbacks on growth and defense by shaping the rhizosphere microbiota. Nature Communications, 2018, 9(1): 2738 https://doi.org/10.1038/s41467-018-05122-7 pmid: 30013066
140	B, Zhong C, Lv W Qin . Effectiveness of the botanical insecticide azadirachtin against Tirathaba rufivena (Lepidoptera: Pyralidae). Florida Entomologist, 2017, 100(2): 215–218 https://doi.org/10.1653/024.100.0215
141	H, Gaspar C, Moiteiro J, Sardinha A González-Coloma . Bioactive semisynthetic dervatives of (S)-(+)-curcuphenol. Natural Product Communications, 2008, 3(9): 1457–1464 https://doi.org/10.1177/1934578X0800300911
142	D, Handayani R A, Edrada P, Proksch V, Wray L, Witte Ofwegen L, van A Kunzmann . New oxygenated sesquiterpenes from the indonesian soft coral nephthea chabrolii. Journal of Natural Products, 1997, 60(7): 716–718 https://doi.org/10.1021/np960699f
143	T, Ishii T, Kamada C S, Phan C S Vairappan . Chabrolene, a novel norditerpene from the bornean soft coral Nephthea sp. Sains Malaysiana, 2018, 47(2): 319–322
144	S, Nobsathian T, Ruttanaphan V Bullangpoti . Insecticidal effects of triterpene glycosides extracted from Holothuria atra (echinodermata: holothuroidea) against Spodoptera litura (Lepidoptera: Noctuidae). Journal of Economic Entomology, 2019, 112(4): 1683–1687 https://doi.org/10.1093/jee/toz075 pmid: 30968940
145	M F, Qiao N Y, Ji X H, Liu K, Li Q M, Zhu Q Z Xue . Indoloditerpenes from an algicolous isolate of Aspergillus oryzae. Bioorganic & Medicinal Chemistry Letters, 2010, 20(19): 5677–5680
146	S, Quiroz-Carreño E, Pastene-Navarrete C, Espinoza-Pinochet E, Muñoz-Núñez L, Devotto-Moreno C L, Céspedes-Acuña J Alarcón-Enos . Assessment of insecticidal activity of benzylisoquinoline alkaloids from Chilean Rhamnaceae plants against fruit-fly Drosophila melanogaster and the Lepidopteran crop pest Cydia pomonella. Molecules, 2020, 25(21): 5094
147	Y L, Wang Z J, Guo G F, Hu G F, Li S J, Niu F Zhao . Separation, identification and pesticidal activity of alkaloids from Anisodus tanguticus (Maxim.). Plant Protection, 2019, 45(04): 190–194, 204 (in Chinese)
148	B G, Zhao Z W, Zhao H G Wang . Inhibitory effects of alkaloids of Sophora alopecuroides on pine wood nematode (Bursaphelenchus xylophilus). Journal of Nanjing Forestry University (Natural Sciences Edition), 2006, 30(06): 129−131
149	W M, Alarif Z S, Abou-Elnaga S E N, Ayyad S S Al-Lihaibi . Insecticidal metabolites from the green alga Caulerpa racemosa. Clean, 2010, 38(5−6): 548−557
150	A, Supriyono B, Schwarz V, Wray L, Witte W E, Müller Soest R, van W, Sumaryono P Proksch . Bioactive alkaloids from the tropical marine sponge Axinella carteri. Zeitschrift für Naturforschung C, 1995, 50(9–10): 669–674
151	R A, Edrada P, Proksch V, Wray L, Witte W E, Müller Soest R W Van . Four new bioactive manzamine-type alkaloids from the Philippine marine sponge Xestospongia ashmorica. Journal of Natural Products, 1996, 59(11): 1056–1060
152	M N, Thompson W A, Gallimore M M, Townsend N A, Chambers L A Williams . Bioactivity of amphitoxin, the major constituent of the Jamaican sponge Amphimedon compressa. Chemistry & Biodiversity, 2010, 7(8): 1904–1910
153	T W, Hong D R, Jímenez T F Molinski . Agelastatins C and D, new pentacyclic bromopyrroles from the sponge Cymbastela sp., and potent arthropod toxicity of (−)-agelastatin A. Journal of Natural Products, 1998, 61(1): 158–161 https://doi.org/10.1021/np9703813 pmid: 9461668
154	R A, Edrada R, Ebel A, Supriyono V, Wray P, Schupp K, Steube Soest R, van P Proksch . Swinhoeiamide A, a new highly active calyculin derivative from the marine sponge Theonella swinhoei. Journal of Natural Products, 2002, 65(8): 1168–1172
155	X, Ji J, Guo Y, Liu A, Lu Z, Wang Y, Li S, Yang Q Wang . Marine-natural-product development: first discovery of nortopsentin alkaloids as novel antiviral, anti-phytopathogenic-fungus, and insecticidal agents. Journal of Agricultural and Food Chemistry, 2018, 66(16): 4062–4072 https://doi.org/10.1021/acs.jafc.8b00507 pmid: 29630371
156	Z, Zuo D Ma . Synthetic studies toward communesins. Israel Journal of Chemistry, 2011, 51(3−4): 434−441
157	F Y, Du X M, Li C S, Li Z, Shang B G Wang . Cristatumins A–D, new indole alkaloids from the marine-derived endophytic fungus Eurotium cristatum EN-220. Bioorganic & Medicinal Chemistry Letters, 2012, 22(14): 4650–4653 https://doi.org/10.1016/j.bmcl.2012.05.088 pmid: 22727636
158	M, Thenmozhi J V, Gopal K, Kannabiran G, Rajakumar K, Velayutham A A Rahuman . Eco-friendly approach using marine actinobacteria and its compounds to control ticks and mosquitoes. Parasitology Research, 2013, 112(2): 719–729 https://doi.org/10.1007/s00436-012-3192-3 pmid: 23180127
159	D, Chen P, Zhang T, Liu X F, Wang Z X, Li W, Li F L Wang . Insecticidal activities of chloramphenicol derivatives isolated from a marine alga-derived endophytic fungus, Acremonium vitellinum, against the cotton bollworm, Helicoverpa armigera (Hübner) (Lepidoptera: Noctuidae). Molecules, 2018, 23(11): 2995 https://doi.org/10.3390/molecules23112995 pmid: 30453532
160	B, Jia Y M, Ma Z, Chen P, Chem Y Hu . Studies on structure and biological activity of indole diketopiperazine alkaloids. Progress in Chemistry, 2018, 30(08): 1067−1081 (in Chinese)
161	C X, Li Y Q, Zhang D, Wang B C, Zhang J X, Lou W Ding . Effects of curcumin and scopoletin on morphological change and water loss of Tetranychus cinnabarinus boisduval (Acarina: Tetranychidae). Journal of Southwest University (Natural Science Edition), 2017, 39(11): 10−15 (in Chinese)
162	K, Georges B, Jayaprakasam S S, Dalavoy M G Nair . Pest-managing activities of plant extracts and anthraquinones from Cassia nigricans from Burkina Faso. Bioresource Technology, 2008, 99(6): 2037–2045 https://doi.org/10.1016/j.biortech.2007.02.049 pmid: 17478091
163	M, Bai C J, Zheng X H, Nong X M, Zhou Y P, Luo G Y Chen . Four new insecticidal xanthene derivatives from the mangrove-derived fungus Penicillium sp. jy246. Marine Drugs, 2019, 17(12): 649 https://doi.org/10.3390/md17120649 pmid: 31756930
164	C, Cui Y, Yang T, Zhao K, Zou C, Peng H, Cai X, Wan R Hou . Insecticidal activity and insecticidal mechanism of total saponins from Camellia oleifera. Molecules, 2019, 24(24): 4518
165	X F, Yang H T, Zhang X X, Chen X Y, Fan Y Zhou . Study on the germicidal effect of four natural products on Helicoverpa armiger. Heilongjiang Grain, 2022, 277(4): 57−63 (in Chinese)
166	Company Monsanto . Determination of nonregulated status for insect resistant cotton. Federal Register, 2021, 86(011): 5130–5131
167	K M, Meepagala U, Bernier C, Burandt S O Duke . Natural products from plants and their synthetic analogs against pests. Planta Medica, 2012, 78(11): PL27 https://doi.org/10.1055/s-0032-1321361
168	Z W, Pan S N, Liu Y C, Chen Y D, Wang Q, Gu D F Song . As natural phytocide: biomarker assessment of Litsea cubeba (Lour.) Persoon essential oil against Drosophila suzukii Matsumura (Diptera: Drosophilidae.). Industrial Crops and Products, 2022, 187: 115421–115426 https://doi.org/10.1016/j.indcrop.2022.115421
169	J Y, Liang Y Y, Yang Y, An Y Z, Shao C Y, He J, Zhang L Y Jia . Insecticidal and acetylcholine esterase inhibition activity of Rhododendron thymifolium essential oil and its main constituent against two stored product insects. Journal of Environmental Science and Health. Part B: Pesticides, Food Contaminants, and Agricultural Wastes, 2021, 56(4): 423–430 https://doi.org/10.1080/03601234.2021.1894888 pmid: 33678144
170	Cropscience Bayer . Patent issued for insect resistant cotton plants and methods for identifying same (USPTO 10356996). Agriculture Week, 2019
171	P P, Kumar S S, Bawani D U, Anandhi K V H Prashanth . Rotenone mediated developmental toxicity in Drosophila melanogaster. Environmental Toxicology and Pharmacology, 2022, 93: 103892
172	M, Díaz C E, Díaz R G, Álvarez A, González L, Castillo A, González-Coloma G, Seoane C Rossini . Differential anti-insect activity of natural products isolated from Dodonaea viscosa Jacq. (Sapindaceae). Journal of Plant Protection Research, 2015, 55(2): 172–178 https://doi.org/10.1515/jppr-2015-0023
173	H, Ikeda N, Yonemochi R, Mikami M, Abe M, Kawamura R, Natsume K, Sakimura J L, Waddington J Kamei . Central dopamine D2 receptors regulate plasma glucose levels in mice through autonomic nerves. Scientific Reports, 2020, 10(1): 22347 https://doi.org/10.1038/s41598-020-79292-0 pmid: 33339892
174	B, Kiss I, Laszlovszky B, Krámos A, Visegrády A, Bobok G, Lévay B, Lendvai V Román . Neuronal dopamine D3 receptors: translational implications for preclinical research and CNS disorders. Biomolecules, 2021, 11(1): 104 https://doi.org/10.3390/biom11010104 pmid: 33466844
175	G, Mao Y, Tian Z, Sun J, Ou H Xu . Bruceine D isolated from Brucea Javanica (L.) Merr. as a systemic feeding deterrent for three major lepidopteran pests. Journal of Agricultural and Food Chemistry, 2019, 67(15): 4232–4239 https://doi.org/10.1021/acs.jafc.8b06511 pmid: 30901209
176	J J, Zhu G J, Brewer D J, Boxler K, Friesen D B Taylor . Comparisons of antifeedancy and spatial repellency of three natural product repellents against horn flies, Haematobia irritans (Diptera: Muscidae). Pest Management Science, 2015, 71(11): 1553–1560 https://doi.org/10.1002/ps.3960 pmid: 25491886
177	I, Coldham S, Dufour T F N, Haxell G P Vennall . Dynamic resolution of N-alkyl-2-lithiopyrrolidines with the chiral ligand (−)-sparteine. Tetrahedron, 2005, 61(13): 3205–3220 https://doi.org/10.1016/j.tet.2005.01.096
178	D, Qin Y, Zhou P, Zhang B, Liu Q, Zheng Z Zhang . Azadirachtin downregulates the expression of the CREB gene and protein in the brain and directly or indirectly affects the cognitive behavior of the Spodoptera litura fourth-instar larvae. Pest Management Science, 2021, 77(4): 1873–1885 https://doi.org/10.1002/ps.6212 pmid: 33284470
179	C S, Vieira M B, Figueiredo C D S, Moraes S B, Pereira P, Dyson C B, Mello D P, Castro P Azambuja . Azadirachtin interferes with basal immunity and microbial homeostasis in the Rhodnius prolixus midgut. Developmental and Comparative Immunology, 2021, 114: 103864 https://doi.org/10.1016/j.dci.2020.103864 pmid: 32918931
180	X B, Huang X C, Wang H Li . Effects of quercetin on the growth and development and detoxification enzymeactivities of Calliptamus abbreviatus. Journal of Northern Agriculture, 2021, 49(2): 71−77 (in Chinese)
181	X, Shao D, Lai W, Xiao W, Yang Y, Yan S Kuang . The botanical eurycomanone is a potent growth regulator of the diamondback moth. Ecotoxicology and Environmental Safety, 2021, 208: 111647 https://doi.org/10.1016/j.ecoenv.2020.111647 pmid: 33396167
182	G, Sharma V Mathur . Modulation of insect-induced oxidative stress responses by microbial fertilizers in Brassica juncea. FEMS Microbiology Ecology, 2020, 96(4): fiaa040
183	B, Cui X, Huang S, Li K, Hao B H, Chang X, Tu B, Pang Z Zhang . Quercetin affects the growth and development of the grasshopper Oedaleus asiaticus (Orthoptera: Acrididae). Journal of Economic Entomology, 2019, 112(3): 1175–1182 https://doi.org/10.1093/jee/toz050 pmid: 30916750
184	J, Dampc M, Kula-Maximenko M, Molon R Durak . Enzymatic defense response of apple aphid Aphis pomi to increased temperature. Insects, 2020, 11(7): 436 https://doi.org/10.3390/insects11070436 pmid: 32664609
185	S Q, Ling B, He D Q, Zeng W W Tang . Effects of botanical pesticide itol A against the tobacco cutworm, Spodoptera litura (Fab.). Environmental Science and Pollution Research International, 2020, 27(11): 12181–12191 https://doi.org/10.1007/s11356-020-07824-2 pmid: 31989496
186	X L, Zhang Y, Wang D, Xu B, Liu H H, Zhang H, Ao G Y Sun . Effect of 1-DNJ from mulberry leaves on the growth and protective enzymes of Spodoptera exigua. Chinese Agricultural Science Bulletin, 2014, 30(22): 316−320 (in Chinese)
187	E, Elzayyat N, Elleboudy A, Moustafa A Ammar . Insecticidal, oxidative, and genotoxic activities of Syzygium aromaticum and Eucalyptus globulus on Culex pipiens adults and larvae. Turkiye Parazitolojii Dergisi, 2018, 42(3): 213–222 https://doi.org/https://pubmed.ncbi.nlm.nih.gov/30280694 pmid: 30280694
188	K, Magierowicz E, Górska-Drabik C Sempruch . The insecticidal activity of Satureja hortensis essential oil and its active ingredient—Carvacrol against Acrobasis advenella (Zinck.) (Lepidoptera, Pyralidae). Pesticide Biochemistry and Physiology, 2019, 153: 122–128 https://doi.org/10.1016/j.pestbp.2018.11.010 pmid: 30744885
189	K A, Bandara V, Kumar U, Jacobsson L P Molleyres . Insecticidal piperidine alkaloid from Microcos paniculata stem bark. Phytochemistry, 2000, 54(1): 29–32 https://doi.org/10.1016/S0031-9422(00)00025-X pmid: 10846743
190	Z, Liu Q, Zhang X, Wu W, Yu S Guo . Insecticidal mechanism of wintergreen oil against the health pest Paederus fuscipes (Coleoptera: Staphylinidae). Journal of Medical Entomology, 2018, 55(1): 155–162 https://doi.org/10.1093/jme/tjx162 pmid: 29029320
191	S, Thapa M, Lv H Xu . Acetylcholinesterase: a primary target for drugs and insecticides. Mini-Reviews in Medicinal Chemistry, 2017, 17(17): 1665–1676 https://doi.org/10.2174/1389557517666170120153930 pmid: 28117022
192	M, Mardani-Talaee V, Rahimi A Zibaee . Effects of host plants on digestive enzymatic activities and some components involved in intermediary metabolism of Chrysodeixis chalcites (Lepidoptera: Noctuidae). Journal of Entomological and Acarological Research, 2014, 46(3): 96–101 https://doi.org/10.4081/jear.2014.3224
193	S, Ranganathan D R, Ampasala B K, Palaka A V, Ilavarasi I, Patidar L P, Poovadan T D Sapam . In silico binding profile analysis and in vitro investigation on chitin synthase substrate and inhibitors from maize stem borer. Chilo partellus. Current Computer-aided Drug Design, 2021, 17(7): 881–895 https://doi.org/10.2174/1573409916666201013150920 pmid: 33109065
194	X, Song C, Liu P, Chen H, Zhang R Sun . Natural product-based pesticide discovery: design, synthesis and bioactivity studies of n-amino-maleimide derivatives. Molecules, 2018, 23(7): 1521 https://doi.org/10.3390/molecules23071521 pmid: 29937519
195	V, Bullangpoti S, Visetson M, Milne J, Milne S, Pornbanlualap C, Sudthongkongs S Tayapat . The novel botanical insecticide for the control brown planthopper (Nilaparvata lugens Stal.). Communications in Agricultural and Applied Biological Sciences, 2006, 71(2 Pt B): 475–481
196	S Q, Li J H, Su Z N Zhang . Effects of rotenone on oviposition and feeding of Monochamus alternatus Hope (Coleoptera: Cerambycidae). Acta Entomologica Sinica, 2005, 48(5): 687−691 (in Chinese)
197	Z Z, Zhou W W You . Progress in the study of rotenone derivatives. Chinese Journal of Organic Chemistry, 2008, 11: 1849−1856 (in Chinese)
198	Y, Zhang Y X, Yuan M, Goto L L, Guo X N, Li S L, Morris-Natschke K H, Lee X J Hao . Taburnaemines A−I, cytotoxic vobasinyl-iboga-type bisindole alkaloids from Tabernaemontana corymbosa. Journal of Natural Products, 2018, 81(3): 562–571
199	U A, Schneider P, Havlík E, Schmid H, Valin A, Mosnier M, Obersteiner H, Böttcher R, Skalský J, Balkovič T, Sauer S Fritz . Impacts of population growth, economic development, and technical change on global food production and consumption. Agricultural Systems, 2011, 104(2): 204–215 https://doi.org/10.1016/j.agsy.2010.11.003
200	C, Rodingpuia H Lalthanzara . An insight into black cutworm (Agrotis ipsilon): a glimpse on globally important crop pest. Science Vision, 2021, 21(2): 36–42 https://doi.org/10.33493/scivis.21.02.02
201	Z R, Song Z Q, Gao J H, He L, Wang X U Qiang . A review of researching present situation and application of pesticides. Journal of Agricultural Mechanization Research, 2007, (7): 10−13 (in Chinese)
202	P, Nicolopoulou-Stamati S, Maipas C, Kotampasi P, Stamatis L Hens . Chemical pesticides and human health: the urgent need for a new concept in agriculture. Frontiers in Public Health, 2016, 4: 148 https://doi.org/10.3389/fpubh.2016.00148 pmid: 27486573
203	C X, Yang J Wang . Research progress in controlled release of pesticides from natural polysaccharides. Hans Journal of Medicinal Chemistry, 2021, 9(2): 62−66 (in Chinese)
204	M, Tudi Ruan H, Daniel L, Wang J, Lyu R, Sadler D, Connell C, Chu D T Phung . Agriculture development, pesticide application and its impact on the environment. International Journal of Environmental Research and Public Health, 2021, 18(3): 1112 https://doi.org/10.3390/ijerph18031112 pmid: 33513796
205	Mojzer E, Brglez Hrnčič M, Knez M, Škerget Ž, Knez U Bren . Polyphenols: extraction methods, antioxidative action, bioavailability and anticarcinogenic effects. Molecules, 2016, 21(7): 901 https://doi.org/10.3390/molecules21070901 pmid: 27409600
206	L, Hu J, Ying M, Zhang X, Qiu Y Lu . Antitumor potential of marine natural products: a mechanistic investigation. Anti-cancer Agents in Medicinal Chemistry, 2018, 18(5): 702–718 https://doi.org/10.2174/1871520617666170918142811 pmid: 28925876
207	R, Kaur R, Sharma G K Chahal . Synthesis of lignin-based hydrogels and their applications in agriculture: a review. Chemical Papers, 2021, 75(9): 4465–4478 https://doi.org/10.1007/s11696-021-01712-w
208	K H, Wei L X, Li Y C, Hang M Y, Wang C, Li J H Miao . Tissue culture of Sophora tonkinensis Gapnep. and its quality evaluation. Pharmacognosy Magazine, 2013, 9(36): 323–330 https://doi.org/10.4103/0973-1296.117828 pmid: 24124284

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