36 results on '"Geng ZF"'
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2. Chemical constituents isolated from stems of Schisandra chinensis and their antifeedant activity against Tribolium castaneum .
- Author
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Guo SS, Pang X, Wang Y, Geng ZF, Cao JQ, Liang JY, Deng ZW, and Du SS
- Subjects
- Animals, Cyclooctanes analysis, Cyclooctanes isolation & purification, Dioxoles isolation & purification, Lignans analysis, Lignans isolation & purification, Polycyclic Compounds isolation & purification, Sesquiterpenes analysis, Sesquiterpenes isolation & purification, Structure-Activity Relationship, Triterpenes analysis, Triterpenes isolation & purification, Cyclooctanes chemistry, Feeding Behavior drug effects, Lignans chemistry, Plant Stems chemistry, Schisandra chemistry, Tribolium drug effects
- Abstract
One new sesquiterpene (α-iso-cubebenol acetate, 8 ), together with 9 known compounds (1-7, 9, 10) were isolated from the stems of Schisandra chinensis (Turcz.) Baill. by repeated silica gel column chromatography. Based on the results of MS, NMR spectra and comparing with literature data, the six dibenzocyclooctadiene lignans were identified as schizandrin A to C (1-3), schizandrin (4), schisantherin A (5) and gomisin J (6), the two sesquiterpenes were identified as α-iso-cubebenol (7) and α-iso-cubebenol acetate (8), while the two triterpenic acids were identified as ganwuweizic acid (9) and kadsuric acid (10). The antifeedant activity of the 10 compounds against Tribolium castaneum adults was tested. Gomisin J (6) exhibited activity at 1500 ppm concentration with 40.3% antifeeding index percentages. As for the dibenzocyclooctene lignans (compounds 1-3 , 6 ), the number of methylenedioxies and the position of hydroxyl groups were the main factors to affect their antifeedant activities.
- Published
- 2020
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3. Contact toxicity and repellent efficacy of Valerianaceae spp. to three stored-product insects and synergistic interactions between two major compounds camphene and bornyl acetate.
- Author
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Feng YX, Wang Y, Geng ZF, Zhang D, Almaz B, and Du SS
- Subjects
- Animals, Coleoptera, Gas Chromatography-Mass Spectrometry, Insect Repellents analysis, Insecta, Insecticides analysis, Oils, Volatile chemistry, Bicyclic Monoterpenes chemistry, Camphanes chemistry, Insect Repellents toxicity, Valerianaceae
- Abstract
In this work, the essential oil (EO) and supercritical CO
2 fluid extract (SF extract) of four Valerianaceae plants (Valeriana officinalis L., Valeriana officinalis L. var. latifolia Miq., Valeriana jatamansi Jones and Nardostachys chinensis Bat.) were chemically characterized. GC-MS analysis identified 74 compounds, representing 35.2%-82.4% of the total EOs and SF extracts. The EO was dominated by low-molecular-weight components while the SF extract was rich in fatty acids. Bornyl acetate and camphene were the characteristic compounds in EO and SF extracts. The efficacy of six extracts against three stored-product insects was investigated. In contact assays, V. officinalis exhibited strongest toxicity to red flour beetle (LD50 = 10.0 μg/adult), and V. jatamansi EO was the most active one against the cigarette beetle (LD50 = 17.6 μg/adult), while V. officinalis var. latifolia EO showed outstanding efficacy against the booklouse (LD50 = 40.2 μg/cm2 ). Binary mixtures of two major compounds (camphene and bornyl acetate) were assessed for the contact toxicity to the red flour beetle. Additive effect existed in the natural proportion of V. officinalis, and synergism was observed in that of V. officinalis var. latifolia. This work confirmed the insecticidal efficacy of the species of the Valerianaceae family, and it would offer some information for the development of botanical insecticide., (Copyright © 2019 The Author(s). Published by Elsevier Inc. All rights reserved.)- Published
- 2020
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4. Insecticidal and repellent efficacy against stored-product insects of oxygenated monoterpenes and 2-dodecanone of the essential oil from Zanthoxylum planispinum var. dintanensis.
- Author
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Wang Y, Zhang LT, Feng YX, Guo SS, Pang X, Zhang D, Geng ZF, and Du SS
- Subjects
- Acyclic Monoterpenes, Animals, Coleoptera drug effects, Gas Chromatography-Mass Spectrometry, Insect Repellents chemistry, Insecticides chemistry, Lethal Dose 50, Monoterpenes analysis, Oxidation-Reduction, Tribolium chemistry, Insect Repellents pharmacology, Insecticides analysis, Monoterpenes chemistry, Oils, Volatile chemistry, Terpenes chemistry, Zanthoxylum chemistry
- Abstract
Essential oils (EOs) extracted from leaves (EL) and fruit pericarp (EFP) of Zanthoxylum planispinum var. dintanensis were analyzed for their chemical composition by GC-MS technique and evaluated for their fumigant, contact toxicity and repellency against three stored-product insects, namely Tribolium castaneum, Lasioderma serricorne, and Liposcelis bostrychophila adults. Results of GC-MS analysis manifested that EL and EFP of Z. planispinum var. dintanensis were mainly composed of oxygenated monoterpenes. Major components included linalool, sylvestrene and terpinen-4-ol. The obvious variation observed between two oil samples was that EL contained 2-dodecanone (11.52%) in addition to the above mentioned components, while this constituent was not detected in EFP. Bioassays of insecticidal and repellent activities were performed for EL, EFP as well as some of their individual compounds (linalool, terpinen-4-ol and 2-dodecanone). Testing results indicated that EL, EFP, linalool, terpinen-4-ol and 2-dodecanone exhibited potent insecticidal and repellent activities against the three target insects selected. Among the three individual compounds, 2-dodecanone was significantly toxic to T. castaneum (LD
50 = 5.21 μg/adult), L. serricorne (LD50 = 2.54 μg/adult) and L. bostrychophila (LD50 = 23.41 μg/cm2 ) in contact assays and had beneficial repellent effects on L. serricorne at 2 and 4 h post-exposure. The anti-insect efficacy of Z. planispinum var. dintanensis EO suggests it has potential to be used as botanical insecticide or repellent to control pest damage in warehouses and grain stores.- Published
- 2019
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5. Seven herbs against the stored product insect: Toxicity evidence and the active sesquiterpenes from Atractylodes lancea.
- Author
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Guo SS, Wang Y, Pang X, Geng ZF, Cao JQ, and Du SS
- Subjects
- Animals, Gas Chromatography-Mass Spectrometry, Insect Repellents chemistry, Insect Repellents isolation & purification, Oils, Volatile, Sesquiterpenes chemistry, Sesquiterpenes isolation & purification, Atractylodes chemistry, Drugs, Chinese Herbal chemistry, Insecticides chemistry, Insecticides isolation & purification, Tribolium
- Abstract
In this work, the essential oils (EO) were extracted from seven typical Chinese herbs, and their repellent and contact toxicities against Tribolium castaneum adults (red flour beetles) were evaluated. The experimental results showed that the above EOs presented the various levels of repellent and contact toxicities. The EOs extracted from A. lancea and A argyi of the Compositae (Asteraceae) family presented obvious repellent effects (Repellency Percentage > 90% at 3.15 nL/cm
2 after 4 h exposure) and strong contact toxicity with LD50 values of 5.78 and 3.09 μg/adult respectively. Based on literature researches and screening results, the EO from A. lancea was analyzed by GC-MS and chosen for further identification of bioactive components. Altogether 59 chemical components were identified and 17 of them were recognized as sesquiterpene compounds, accounting for 57.8% of the total weight of the EO. From the identified sesquiterpenes, three individual compounds (β-eudesmol, hinesol, valencene) were selected for the laboratory bioassays of the toxicity against red flour beetles. It was found that all the three compounds expressed some repellent effects. Although β-eudesmol (31.2%) and hinesol (5.1%) were identified as main constituents and had been considered to be symbolic characteristics of high medicinal value, valencene (0.3%) showed strong repellent property which could be comparable to that of DEET (N, N‑diethyl‑3‑methylbenzamide), a powerful commercial pesticides, and it had best toxicity with LD50 values of 3.25 (μg/adult) in the contact test. This work may provide toxicity evidence of seven common herbs against red flour beetles, add the information for the development and comprehensive utilization of A. lancea, and will contribute to the application of grain preservation., (Copyright © 2018 Elsevier Inc. All rights reserved.)- Published
- 2019
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6. Toxicity and repellency of essential oil from Evodia lenticellata Huang fruits and its major monoterpenes against three stored-product insects.
- Author
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Cao JQ, Guo SS, Wang Y, Pang X, Geng ZF, and Du SS
- Subjects
- Animals, Fruit, Gas Chromatography-Mass Spectrometry, Insect Repellents analysis, Insect Repellents pharmacology, Insecticides analysis, Insecticides pharmacology, Monoterpenes analysis, Monoterpenes pharmacology, Oils, Volatile analysis, Oils, Volatile pharmacology, Phytochemicals analysis, Phytochemicals pharmacology, Evodia, Insect Repellents toxicity, Insecticides toxicity, Monoterpenes toxicity, Neoptera drug effects, Oils, Volatile toxicity, Phytochemicals toxicity
- Abstract
In this work, the essential oil (EO) was extracted from the fruits of Evodia lenticellata, and the fumigant toxicity, contact toxicity and repellency against three stored-product insect species were evaluated for the obtained EO and several of its chemical components. The target insects were the adults of Tribolium castaneum (Coleoptera: Tenebrionidae), Lasioderma serricorne (Coleoptera: Anobiidae) and Liposcelis bostrychophila (Psocoptera: Liposcelididae). The EO was obtained with hydrodistillation and its chemical components were analyzed with the gas chromatography-mass spectrometry (GC-MS). Twenty-seven compounds, accounting for 83.1% of the total amount of the oil, were identified from the EO sample. The main compounds included linalool (12.0%), β-pinene (11.5%), 3-carene (9.6%), caryophyllene oxide (8.7%) and β-caryophyllene (7.9%). Among them, the amounts of monoterpenes and sesquiterpenes were as high as 52.7% and 22.7% to the total amount of EO respectively. The results of bioactivity test showed that the EO and its testing compounds had interspecific toxicity and repellent activity. So that, it might be expected that the EO extracted from the fruits of E. lenticellata could be developed to a new type of eco-friendly natural insecticide or repellent for the control of stored-product insects., (Copyright © 2018 Elsevier Inc. All rights reserved.)
- Published
- 2018
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7. Supercritical carbon dioxide extract of Cinnamomum cassia bark: toxicity and repellency against two stored-product beetle species.
- Author
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Wang Y, Dai PP, Guo SS, Cao JQ, Pang X, Geng ZF, Sang YL, and Du SS
- Subjects
- Animals, Carbon Dioxide, Chromatography, Supercritical Fluid, Gas Chromatography-Mass Spectrometry, Plant Bark chemistry, Plant Extracts chemistry, Cinnamomum aromaticum chemistry, Insect Repellents analysis, Insecticides analysis, Tribolium
- Abstract
The extract from Cinnamomum cassia Presl bark was obtained with supercritical CO
2 fluid extraction (SFE). Chemical components of the SFE extract were characterized by GC-MS spectrometry. The repellency and contact toxicity of the SFE extract were evaluated against the adults of Tribolium castaneum and Lasioderma serricorne along with those of its two main compounds. The results of GC-MS analysis indicated that 33 volatile constituents were identified from the extract. The main components included trans-cinnamaldehyde (32.1%), 3,3-dimethylhexane (10.6%) and 2,4-di-tert-butylphenol (7.9%). Testing results showed that the SFE extract had potent contact toxicity against T. castaneum and L. serricorne with LD50 values of 3.96 and 23.89 μg/adult, respectively. LD50 values of trans-cinnamaldehyde against T. castaneum and L. serricorne were 5.78 and 3.24 μg/adult, respectively. Additionally, percentage repellency values of the SFE extract and trans-cinnamaldehyde against T. castaneum and L. serricorne were rather high (PR = 100% and PR > 90%, respectively) at 78.63 and 15.73 nL/cm2 at 2 h post-exposure. 2,4-Di-tert-butylphenol showed some repellency against both beetle species. Considering its insecticidal and repellent effects, the SFE extract from C. cassia bark might be used in integrated pest management programs for T. castaneum and L. serricorne.- Published
- 2018
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8. Contact Toxicity and Repellency of the Essential Oils of Evodia lenticellata Huang and Evodia rutaecarpa (Juss.) Benth. Leaves against Three Stored Product Insects.
- Author
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Cao JQ, Guo SS, Wang Y, Pang X, Geng ZF, and Du SS
- Subjects
- Acyclic Monoterpenes, Alkenes analysis, Alkenes toxicity, Animals, Bicyclic Monoterpenes, Distillation methods, Gas Chromatography-Mass Spectrometry, Monoterpenes analysis, Monoterpenes toxicity, Oils, Volatile isolation & purification, Polycyclic Sesquiterpenes, Sesquiterpenes analysis, Sesquiterpenes toxicity, Coleoptera drug effects, Evodia chemistry, Insect Repellents, Oils, Volatile chemistry, Oils, Volatile toxicity, Plant Leaves chemistry, Tribolium drug effects
- Abstract
The essential oils (EOs) extracted from Evodia lenticellata Huang and Evodia rutaecarpa (Juss.) Benth. leaves are screened to evaluate their contact toxicity and repellency towards Tribolium castaneum (Coleoptera: Tenebrionidae), Lasioderma serricorne (Coleoptera: Anobiidae) and Liposcelis bostrychophila (Psocoptera: Liposcelididae) adults. The EOs are obtained by hydrodistillation and analyzed by gas chromatography-mass spectrometry (GC-MS). The principal components in the E. lenticellata EO are identified to be caryophyllene oxide (28.5%), β-caryophyllene (23.1%), β-elemene (14.5%), and β-cubebene (4.7%), while the main components of the E. rutaecarpa EO are α-pinene (39.4%), β-elemene (13.5%), α-ocimene (7.6%), and α-selinene (4.0%). These two kinds of EOs and their individual compounds all showed different levels of contact toxicity and repellent activity against three stored-product insects.
- Published
- 2018
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9. Fumigant and repellent activities of essential oil extracted from Artemisia dubia and its main compounds against two stored product pests.
- Author
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Liang JY, Guo SS, Zhang WJ, Geng ZF, Deng ZW, Du SS, and Zhang J
- Subjects
- Animals, Cyclohexane Monoterpenes, Cyclohexenes pharmacology, Food Storage, Insect Control methods, Insect Repellents chemistry, Limonene, Terpenes pharmacology, Artemisia chemistry, Insect Repellents pharmacology, Oils, Volatile chemistry, Phthiraptera drug effects, Tribolium drug effects
- Abstract
The major chemical constituents of the essential oil extracted from Artemisia dubia wall. ex Bess. (Family: Asteraceae) were found as terpinolene (19.02%), limonene (17.40%), 2,5-etheno[4.2.2]propella-3,7,9-triene (11.29%), isoelemicin (11.05%) and p-cymene-8-ol (5.93%). Terpinolene and limonene were separated as main components from the essential oil. The essential oil showed fumigant toxicity against Tribolium castaneum and Liposcelis bostrychophila with LC
50 values of 49.54 and 0.74 mg/L, respectively. The essential oil and isolated compounds of A. dubia showed repellency activities against both insects. Terpinolene and limonene showed the fumigant toxicity against T. castaneum. Terpinolene showed obvious fumigant toxicity against L. bostrychophila. The results indicated that the essential oil of A. dubia had potential to be developed into natural insecticides for controlling stored product pests.- Published
- 2018
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10. Chemical Constituents of Murraya tetramera Huang and Their Repellent Activity against Tribolium castaneum.
- Author
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You CX, Guo SS, Zhang WJ, Geng ZF, Liang JY, Lei N, Du SS, and Deng ZW
- Subjects
- Animals, Magnetic Resonance Spectroscopy, Molecular Structure, Insect Repellents chemistry, Insect Repellents pharmacology, Murraya chemistry, Plant Extracts chemistry, Tribolium drug effects
- Abstract
Sixteen compounds were isolated from the leaves and stems of Murraya tetramera Huang. Based on the NMR and MS spectral results, the structures were determined. It was confirmed that the isolated compounds included three new compounds ( 9 , 10 and 13 ) and one new natural product ( 8 ), which were identified asmurratetra A ( 9 ), murratetra B ( 10 ), murratetra C ( 13 ) and [2-(7-methoxy-2-oxochromen-8-yl)-3-methylbut-2-enyl]3-methylbut-2-enoate ( 8 ), respectively. Meanwhile, the repellent activity against Tribolium castaneum was investigated for 13 of these isolated compounds. The results showed that the tested compounds had various levels of repellent activity against T. castaneum . Among them, compounds 1 (4(15)-eudesmene-1β,6α-diol), 11 (isoferulic acid) and 16 (2,3-dihydroxypropyl hexadecanoate) showed fair repellent activity against T. castaneum . They might be considered as potential leading compounds for the development of natural repellents., Competing Interests: The authors declare no conflict of interest.
- Published
- 2017
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11. Kinetic studies of the strengthening effect on liquid hot water pretreatments by organic acids.
- Author
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Lyu H, Lv C, Zhang M, Liu J, Meng F, and Geng ZF
- Subjects
- Hydrolysis, Kinetics, Water, Acetic Acid metabolism, Xylose metabolism
- Abstract
The liquid hot water (LHW) pretreatments would be accelerated by the organic acids produced from the process. In the study, the organic acids included not only acetic acid but also lactic acid during LHW hydrolysis of reeds, at 180-220°C and for 15-135min. The lactic acid was presumably produced from xylose degradation in the pretreatment process. The different organic acids, such as acetic acid, lactic acid and acetic-lactic acids, were used to strengthen the LHW pretreatments for increasing xylose production. Moreover, the work presented kinetic models of xylose and hemicellulose at different conditions, considering the generation of lactic acid. The experimental and kinetic results both indicated that acetic-lactic acids had synergistic catalytic effect on the reaction, which could not only inhibit the degradation of xylose, but also promote the hydrolysis of hemicellulose. Besides, the highest concentration of xylose of 7.323g/L was obtained at 200°C, for 45min and with 1wt% acetic-lactic acids., (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Published
- 2017
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12. Repellence of the main components from the essential oil of Glycosmis lucida Wall. ex Huang against two stored product insects.
- Author
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Guo SS, Zhang WJ, Yang K, Liang JY, You CX, Wang CF, Li YP, Geng ZF, Deng ZW, and Du SS
- Subjects
- Allylbenzene Derivatives, Animals, Anisoles pharmacology, Oils, Volatile analysis, Tribolium, Insect Repellents pharmacology, Oils, Volatile pharmacology, Rutaceae chemistry
- Abstract
A screening of Chinese medicinal herbs and wild plants for agrochemicals was carried out; the essential oil of Glycosmis lucida leaves was found to possess significant repellent activity against Tribolium castaneum and Liposcelis bostrychophila. It was found that the main components included elixene (19.81%), spathulenol (10.68%), anethole (12.05%), verbenone (10.32%) followed by β-caryophyllene (6.87%). The essential oil, anethole and verbenone were strongly repellent against T. castaneum (96, 86 and 94%, respectively, at 15.73 nL cm
-2 ) and L. bostrychophila (100, 68 and 72%, respectively, at 31.58 nL cm-2 ) after a 2h treatment. The results indicate that anethole and verbenone had the potential to be developed as natural repellents for control of stored product insects.- Published
- 2017
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13. NMR solution structure study of one saturated sulphur-containing amides from Glycosmis lucida.
- Author
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Geng ZF, Yang K, Li YP, Guo SS, You CX, Zhang WJ, Zhang Z, and Du SS
- Subjects
- Amides chemistry, Magnetic Resonance Spectroscopy methods, Mass Spectrometry, Molecular Structure, Sulfonamides chemistry, Sulfur chemistry, Rutaceae chemistry
- Abstract
One sulphur-containing amide (N-[2-(4-Hydroxyphenyl)-ethyl]-3-methanesulfonyl-N-methyl-propionamide) which was isolated from Glycosmis lucida Wall ex Huang had a different NMR profile with this kind of compounds' normal case. Based on the information obtained by nuclear magnetic resonance pectroscopy (NMR) and mass spectrometry (MS), its configurations in solution were investigated. The results indicated that the compound would have two stable configurations in solution as the double bond switched between C-N and C-O in an appropriate rate. This phenomenon was clearly exposed by the one dimension selective NOE (1D-NOE) experiments. This conclusion would play an active role in the structure analysis work of this kind of compounds.
- Published
- 2017
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14. 1 H and 13 C NMR spectral assignments of a new cyclic peptide from Glycosmis lucida Wall. Ex Huang.
- Author
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Geng ZF, Yang K, Guo SS, Zhang WJ, You CX, Liang JY, Deng ZW, and Du SS
- Subjects
- Chromatography, High Pressure Liquid, Plant Leaves chemistry, Protein Conformation, Carbon-13 Magnetic Resonance Spectroscopy methods, Peptides, Cyclic chemistry, Proton Magnetic Resonance Spectroscopy methods, Rutaceae chemistry
- Published
- 2016
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15. Chemical Composition of Essential Oils from Zanthoxylum bungeanum Maxim. and Their Bioactivities against Lasioderma serricorne.
- Author
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Zhang WJ, Guo SS, You CX, Geng ZF, Liang JY, Deng ZW, Wang CF, Du SS, and Wang YY
- Subjects
- Animals, Chromatography, Supercritical Fluid, Distillation, Fatty Acids analysis, Fatty Acids isolation & purification, Gas Chromatography-Mass Spectrometry, Monoterpenes analysis, Monoterpenes isolation & purification, Sesquiterpenes analysis, Sesquiterpenes isolation & purification, Coleoptera drug effects, Insect Repellents analysis, Insect Repellents isolation & purification, Insecticides analysis, Insecticides isolation & purification, Plant Oils analysis, Plant Oils isolation & purification, Zanthoxylum chemistry
- Abstract
Two essential oil samples were obtained from the pericarp of Zanthoxylum bungeanum with the methods of hydrodistillation (HD) and supercritical fluid CO
2 extraction (SFE), their chemical components were identified, and their bioactivities against Lasioderma serricorne adults were evaluated. In the process of testing, the two samples showed significant bioactivities against Lasioderma serricorne adults. For an example, the SFE-sample expressed relatively stronger fumigant toxicity on Lasioderma serricorne adults (LC50 = 3.99 μg/mL air) than that of the HD-sample (LC50 = 12.54 μg/mL air). According to GC-MS analysis, the chemical components between two samples were different. The major chemical components for HD included linalool (25.99%), limonene (19.34%), linalyl anthranilate (12.22%), 4-terpinenol (10.49%), eucalyptol (6.53%) and α-terpineol (5.02%), while for SFE included nonanoic acid (21.43%), γ-terpinene (14.51%), eucalyptol (13.45%), α-terpineol (5.83%) and caryophyllene oxide (5.48%). The results showed that different chemical components result in different bioactivities. This work provides theoretical basis for traditional Chinese concept of antagonistic storage, and it also provides important information for the development and comprehensive utilization of Zanthoxylum bungeanum.- Published
- 2016
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16. Chemical Constituents and Insecticidal Activities of Ajania fruticulosa Essential Oil.
- Author
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Liang JY, Guo SS, You CX, Zhang WJ, Wang CF, Geng ZF, Deng ZW, Du SS, and Zhang J
- Subjects
- Animals, Dose-Response Relationship, Drug, Insecticides chemical synthesis, Insecticides chemistry, Oils, Volatile chemical synthesis, Oils, Volatile chemistry, Asteraceae chemistry, Insecta drug effects, Insecticides pharmacology, Oils, Volatile pharmacology
- Abstract
The insecticidal activity and chemical constituents of the essential oil from Ajania fruticulosa were investigated. Twelve constituents representing 91.0% of the essential oil were identified, and the main constituents were 1,8-cineole (41.40%), (+)-camphor (32.10%), and myrtenol (8.15%). The essential oil exhibited contact toxicity against Tribolium castaneum and Liposcelis bostrychophila adults with LD50 values of 105.67 μg/adult and 89.85 μg/cm(2) , respectively. The essential oil also showed fumigant toxicity against two species of insect with LC50 values of 11.52 and 0.65 mg/l, respectively. 1,8-Cineole exhibited excellent fumigant toxicity (LC50 = 5.47 mg/l) against T. castaneum. (+)-Camphor showed obvious fumigant toxicity (LC50 = 0.43 mg/l) against L. bostrychophila. Myrtenol showed contact toxicity (LD50 = 29.40 μg/cm(2) ) and fumigant toxicity (LC50 = 0.50 mg/l) against L. bostrychophila. 1,8-Cineole and (+)-camphor showed strong insecticidal activity to some important insects, and they are main constituents of A. fruticulosa essential oil. The two compounds may be related to insecticidal activity of A. fruticulosa essential oil against T. castaneum and L. bostrychophila., (© 2016 Wiley-VHCA AG, Zürich.)
- Published
- 2016
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17. Chemical Constituents and Activity of Murraya microphylla Essential Oil against Lasioderma serricorne.
- Author
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You CX, Guo SS, Zhang WJ, Yang K, Wang CF, Geng ZF, Du SS, Deng ZW, and Wang YY
- Subjects
- Animals, Insect Repellents chemistry, Insecticides chemistry, Oils, Volatile chemistry, Plant Oils chemistry, Coleoptera drug effects, Insect Repellents pharmacology, Insecticides pharmacology, Murraya chemistry, Oils, Volatile pharmacology, Plant Oils pharmacology
- Abstract
The chemical composition, contact and repellent activities of the essential oil from Murraya microphylla branches and leaves against Lasioderma serricorne adults were determined and six compounds from the essential oil were isolated as well. The essential oil of M microphylla obtained by hydrodistillation was analyzed by gas chromatography-mass spectrometric (GC-MS) analysis; 22 compounds were identified. The main constituents of the essential oil included β-caryophyllene (18.0%), α-pinene (13.8%), spathulenol (9.5%), α-humulene (6.0%), γ-elemene (5.1%) and zingiberene (4.6%), followed by α-cadinol (3.9%) and caryophyllene oxide (3.8%). Six of these compounds were isolated and fully identified as α-pinene, β-caryophyllene, α-humulene, caryophyllene oxide, spathulenol and α-cadinol. L. serricorne adults had different sensitivities to the crude essential oil and isolated compounds. α-Humulene exhibited the strongest contact activity against L. serricorne, showing an LD50 value of 13.1 µg adult(-1). However, spathulenol, the crude essential oil and α-cadinol showed stronger contact activity against L. serricorne than caryophyllene oxide and β-caryophyllene. The essential oil, α-humulene and spathulenol showed comparable repellency against L. serricorne adults at 2 h after exposure, relative to the positive control, DEET. The results demonstrate that the essential oil and isolated compounds exhibited important contact and repellent activities against L. serricorne. Thus, they could become potential natural insecticides or repellents for control of insects in stored products.
- Published
- 2015
18. Chemical Composition and Bioactivities of the Essential Oil from Etlingera yunnanensis against Two Stored Product Insects.
- Author
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Guo SS, You CX, Liang JY, Zhang WJ, Geng ZF, Wang CF, Du SS, and Lei N
- Subjects
- Animals, Insect Repellents chemistry, Insect Repellents pharmacology, Insecticides chemistry, Insecticides pharmacology, Rhizome chemistry, Insecta drug effects, Oils, Volatile analysis, Oils, Volatile pharmacology, Zingiberaceae chemistry
- Abstract
The chemical composition of the essential oil of Etlingera yunnanensis rhizomes and its contact and repellent activities against Tribolium castaneum (Herbst) and Liposcelis bostrychophila (Badonnel) were investigated. The essential oil obtained from E. yunnanensis rhizomes with hydrodistillation was performed by gas chromatography-flame ionization detection and gas chromatography-mass spectrometry. The main components of the essential oil were identified to be estragole (65.2%), β-caryophyllene (6.4%), 1,8-cineole (6.4%), limonene (5.2%), and α-pinene (2.4%). It was found that the essential oil of E. yunnanensis rhizomes possessed contact toxicity against T. castaneum and L. bostrychophila (LD50 = 23.33 μg/adult and LD50 = 47.38 μg/cm², respectively). Estragole, 1,8-cineole, and limonene exhibited stronger contact toxicity (LD50 values of 20.41, 18.86, and 13.40 μg/adult, respectively) than β-caryophyllene (LD50 = 41.72 μg/adult) against T. castaneum adults. Estragole possessed stronger contact toxicity (LD50 = 30.22 µg/cm²) than β-caryophyllene, 1,8-cineole, and limonene (LD50 values of 74.11, 321.20, and 239.62 μg/adult, respectively) against L. bostrychophila adults. Repellency of the crude oil was also evaluated. The essential oil and constituents possessed strong repellent activity against T. castaneum adults. The four individual constituents showed weaker repellent activity than the essential oil against L. bostrychophila adults. The results indicated that the essential oil of E. yunnanensis rhizomes and the individual constituents had the potential to be developed as a natural insecticide and repellent for the control of T. castaneum and L. bostrychophila.
- Published
- 2015
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19. Contact Toxicity and Repellency of the Main Components From the Essential Oil of Clausena anisum-olens Against Two Stored Product Insects.
- Author
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You CX, Jiang HY, Zhang WJ, Guo SS, Yang K, Lei N, Ma P, Geng ZF, and Du SS
- Subjects
- Animals, Coleoptera, Clausena chemistry, Insect Repellents, Insecta, Insecticides, Oils, Volatile
- Abstract
The essential oil of Clausena anisum-olens (Blanco) Merr. showed strong contact toxicity and repellency against Lasioderma serricorne and Liposcelis bostrychophila adults. The components of the essential oil obtained by hydrodistillation were determined by gas chromatography-mass spectrometry. It was found that the main components were myristicin (36.87%), terpinolene (13.26%), p-cymene-8-ol (12.38%), and 3-carene (3.88%). Myristicin and p-cymene-8-ol were separated by silica gel column chromatography, and their molecular structures were confirmed by means of physicochemical and spectrometric analysis. Myristicin and p-cymene-8-ol showed strong contact toxicity against L. serricorne (LD50 = 18.96 and 39.68 μg per adult) and Li. bostrychophila (LD50 = 20.41 and 35.66 μg per adult). The essential oil acting against the two grain storage insects showed LD50 values of 12.44 and 74.46 μg per adult, respectively. Myristicin and p-cymene-8-ol have strong repellent toxicity to Li. bostrychophila., (© The Author 2015. Published by Oxford University Press on behalf of the Entomological Society of America.)
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- 2015
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20. Contact Toxicity and Repellency of the Essential Oil of Dictamnus dasycarpus Roots from China against Two Stored-Product Insects.
- Author
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Yang K, Guo SS, Geng ZF, Du SS, Wang CF, and Deng ZW
- Subjects
- Animals, China, Dose-Response Relationship, Drug, Insect Repellents chemistry, Insect Repellents isolation & purification, Insecticides chemistry, Insecticides isolation & purification, Molecular Structure, Oils, Volatile chemistry, Oils, Volatile isolation & purification, Structure-Activity Relationship, Coleoptera drug effects, Dictamnus chemistry, Insect Repellents pharmacology, Insecticides pharmacology, Oils, Volatile pharmacology, Plant Roots chemistry
- Abstract
During our screening program for new agrochemicals from traditional medicinal herbs, Dictamnus dasycarpus was found to possess contact toxicity and repellent activity against the cigarette beetle Lasioderma serricorne and the booklouse Liposcelis bostrychophila. The essential oil obtained by hydrodistillation of D. dasycarpus roots was characterized by GC-FID and GC/MS analyses, and the main components identified were syn-7-hydroxy-7-anisylnorbornene (1, 49.9%), 1,3,4,5,6,7-hexahydro-2H-inden-2-one (2, 11.6%), 5,6-diethenyl-1-methylcyclohexene (3, 7.4%), and 3,9-dimethyltricyclo[4.2.1.1(2,5)]dec-3-en-9-ol (4, 6.35%). The D. dasycarpus root oil exhibited strong contact toxicity against L. serricorne adults and L. bostrychophila, with LD50 values of 12.4 μg/adult and 27.2 μg/cm(2), respectively. Moreover, the essential oil also showed strong repellency against both stored-product insects tested., (Copyright © 2015 Verlag Helvetica Chimica Acta AG, Zürich.)
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- 2015
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21. Bioactivity of Essential Oil of Zingiber purpureum Rhizomes and Its Main Compounds against Two Stored Product Insects.
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Wang Y, You CX, Yang K, Wu Y, Chen R, Zhang WJ, Liu ZL, Du SS, Deng ZW, Geng ZF, and Han J
- Subjects
- Animals, Plant Extracts chemistry, Rhizome chemistry, Coleoptera, Insecticides, Oils, Volatile, Zingiberaceae chemistry
- Abstract
The insecticidal and repellent activities of the essential oil extracted from Zingiber purpureum Roscoe rhizomes were evaluated against Tribolium castaneum (Herbst) and Lasioderma serricorne (L.) adults. During our screening program for agrochemicals from Chinese medicinal herbs and wild plants, the essential oil of Z. purpureum rhizomes was found to possess strong contact toxicity against T. castaneum and L. serricorne adults, with LD50 values of 39.0 and 16.3 µg per adult, respectively, and also showed strong fumigant toxicity against the two grain storage insects with LC50 values of 13.6 and 9.3 mg/liter of air, respectively. The essential oil obtained by hydrodistillation was investigated by gas chromatography-mass spectrometry. The main components of the essential oil were identified to be sabinene (48.1%), terpinen-4-ol (25.1%), and γ-terpinene (6.7%), followed by α-terpinene (4.3%), β-thujene (3.4%), and α-phellandrene (2.7%). Sabinene, terpinen-4-ol, and γ-terpinene were separated and purified by silica gel column chromatography and preparative thin-layer chromatography. Terpinen-4-ol showed the strongest contact toxicity against T. castaneum and L. serricorne (LD50=19.7 and 5.4 µg per adult, respectively) and also the strongest fumigant toxicity against T. castaneum and L. serricorne (LC50=3.7 and 1.3 mg/liter of air, respectively). Otherwise, sabinene and terpinen-4-ol were strongly repellent against T. castaneum as well as the essential oil, while γ-terpinene exhibited weaker repellency against T. castaneum compared with the positive control, DEET (N, N-diethyl-3-methylbenzamide). Moreover, only the essential oil exhibited strong repellency against L. serricorne, the three compounds exhibited weaker repellency against L. serricorne relative to DEET., (© The Authors 2015. Published by Oxford University Press on behalf of Entomological Society of America. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
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- 2015
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22. Chemical Composition and Insecticidal Activity of Essential Oils from Zanthoxylum dissitum Leaves and Roots against Three Species of Storage Pests.
- Author
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Wang CF, Yang K, You CX, Zhang WJ, Guo SS, Geng ZF, Du SS, and Wang YY
- Subjects
- Animals, Insect Repellents chemistry, Insect Repellents pharmacology, Monocyclic Sesquiterpenes, Polycyclic Sesquiterpenes, Sesquiterpenes chemistry, Sesquiterpenes pharmacology, Sesquiterpenes, Germacrane chemistry, Sesquiterpenes, Germacrane pharmacology, Terpenes chemical synthesis, Terpenes chemistry, Terpenes pharmacology, Coleoptera drug effects, Insecticides chemistry, Insecticides pharmacology, Oils, Volatile chemistry, Oils, Volatile pharmacology, Plant Leaves chemistry, Plant Roots chemistry, Zanthoxylum chemistry
- Abstract
This work aimed to investigate chemical composition of essential oils obtained from Zanthoxylum dissitum leaves and roots and their insecticidal activities against several stored product pests, namely the cigarette beetle (Lasioderma serricorne), red flour beetle (Tribolium castaneum) and black carpet beetle (Attagenus piceus). The analysis by GC-MS of the essential oils allowed the identification of 28 and 22 components, respectively. It was found that sesquiterpenoids comprised a fairly high portion of the two essential oils, with percentages of 74.0% and 80.9% in the leaves and roots, respectively. The main constituents identified in the essential oil of Z. dissitum leaves were δ-cadinol (12.8%), caryophyllene (12.7%), β-cubebene (7.9%), 4-terpineol (7.5%) and germacrene D-4-ol (5.7%), while humulene epoxide II (29.4%), caryophyllene oxide (24.0%), diepicedrene-1-oxide (10.7%) and Z,Z,Z-1,5,9,9-tetramethyl-1,4,7-cycloundecatriene (8.7%) were the major components in the essential oil of Z. dissitum roots. The insecticidal activity results indicated that the essential oil of Z. dissitum roots exhibited moderate contact toxicity against three species of storage pests, L. serricorne,T. castaneum and A. piceus, with LD50 values of 13.8, 43.7 and 96.8 µg/adult, respectively.
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- 2015
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23. Contact toxicity and repellency of the essential oil from Mentha haplocalyx Briq. against Lasioderma serricorne.
- Author
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Zhang WJ, Yang K, You CX, Wang CF, Geng ZF, Su Y, Wang Y, Du SS, and Deng ZW
- Subjects
- Animals, Dose-Response Relationship, Drug, Gas Chromatography-Mass Spectrometry, Insect Repellents chemistry, Insecticides chemistry, Insecticides isolation & purification, Oils, Volatile chemistry, Oils, Volatile isolation & purification, Plant Oils chemistry, Plant Oils isolation & purification, Coleoptera drug effects, Insect Repellents toxicity, Insecticides toxicity, Mentha chemistry, Oils, Volatile toxicity, Plant Oils toxicity
- Abstract
The chemical composition of the essential oil obtained by hydrodistillation from the aerial parts of Mentha haplocalyx was investigated by GC-FID and GC/MS analyses. In sum, 23 components, representing 92.88% of the total oil composition, were identified, and the main compounds were found to be menthol (59.71%), menthyl acetate (7.83%), limonene (6.98%), and menthone (4.44%). By bioassay-guided fractionation (contact toxicity), three compounds were obtained from the essential oil and identified as menthol, menthyl acetate, and limonene. The essential oil and the three isolated compounds exhibited potent contact toxicity against Lasioderma serricorne adults, with LD50 values of 16.5, 7.91, 5.96, and 13.7 μg/adult, respectively. Moreover, the oil and its isolated compounds also exhibited strong repellency against L. serricorne adults. At the lower concentrations tested and at 2 h after exposure, menthol showed even significantly stronger repellency than the positive control DEET. The study revealed that the bioactivity properties of the essential oil can be attributed to the synergistic effects of its diverse major and minor components, which indicates that the M. haplocalyx oil and its isolated compounds have potential for the development as natural insecticides and/or repellents to control insects in stored grains and traditional Chinese medicinal materials., (Copyright © 2015 Verlag Helvetica Chimica Acta AG, Zürich.)
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- 2015
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24. Insecticidal and repellant activities of polyacetylenes and lactones derived from Atractylodes lancea rhizomes.
- Author
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Chen HP, Zheng LS, Yang K, Lei N, Geng ZF, Ma P, Cai Q, Du SS, and Deng ZW
- Subjects
- Animals, Dose-Response Relationship, Drug, Drug Evaluation, Preclinical methods, Furans pharmacology, Insect Repellents chemistry, Insecticides chemistry, Lactones pharmacology, Magnetic Resonance Spectroscopy, Rhizome chemistry, Sesquiterpenes pharmacology, Structure-Activity Relationship, Tribolium drug effects, Atractylodes chemistry, Insect Repellents pharmacology, Insecticides pharmacology, Polyynes chemistry, Polyynes pharmacology
- Abstract
During a screening program for new agrochemicals from Chinese medicinal herbs and local wild plants, the petroleum ether (PE) extract of Atractylodes lancea (Thunb.) rhizomes was found to possess repellent and contact activities against Tribolium castaneum adults. Bioactivity-directed chromatographic separation of PE extract on repeated silica-gel columns led to the isolation of two polyacetylenes, atractylodin and atractylodinol (1 and 2, resp.), and two lactones, atractylenolides II and III (3 and 4, resp.). The structures of the compounds were elucidated based on NMR spectra. The four isolated compounds were evaluated for their insecticidal and repellent activities against T. castaneum. Atractylodin exhibited strong contact activity against T. castaneum adults with a LD50 value of 1.83 μg/adult. Atractylodin and atractylenolide II also possessed strong repellenct activities against T. castaneum adults. After 4-h exposure, >90% repellency was achieved with atractylodin at a low concentration of 0.63 μg/cm(2) . The results indicated that atractylodin (1) and atractylenolide II (3) have a good potential as a source for natural repellents, and 1 has the potential to be developed as natural insecticide., (Copyright © 2015 Verlag Helvetica Chimica Acta AG, Zürich.)
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- 2015
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25. Insecticidal Constituents of Essential Oil Derived from Zanthoxylum armatum against Two Stored-Product Insects.
- Author
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Wang CF, Zhang WJ, You CX, Guo SS, Geng ZF, Fan L, Du SS, Deng ZW, and Wang YY
- Subjects
- Animals, Chromatography, Gas, Dose-Response Relationship, Drug, Flame Ionization, Food Contamination prevention & control, Food Storage, Fumigation, Gas Chromatography-Mass Spectrometry, Oils, Volatile chemistry, Oils, Volatile isolation & purification, Oils, Volatile toxicity, Plant Oils chemistry, Plant Oils isolation & purification, Plant Oils toxicity, Coleoptera drug effects, Insecticides, Oils, Volatile pharmacology, Plant Oils pharmacology, Zanthoxylum chemistry
- Abstract
In the course of our search for natural bioactive chemicals and investigations on their insecticidal activities from some medicinal plants growing in China, the essential oil derived from the twigs of Zanthoxylum armatum (Rutaceae) was found to possess strong insecticidal activities against two stored-product insects, Lasioderma serricorne and Tribolium castaneum. A total of 32 constituents of the essential oil were identified by GC and GC-MS analysis, and it revealed (E)-anethole (20.5%), 1,8-cineole (14.0%), 2-tridecanone (12.5%), limonene (9.0%) and piperitone (8.0%) as major components, followed by β-phellandrene (6.3%), β-pinene (5.1%) and 4-terpineol (4.4%). From the essential oil, five compounds were isolated and identified as (E)-anethole, 1,8-cineole, 2-tridecanone, limonene and piperitone. The results of insecticidal bioassays showed that the essential oil of Z. armatum exhibited strong fumigant toxicity towards L. serricorne and T. castaneum with LC50 values of 13.83 and 4.28 mg/L air, respectively, and also possessed contact toxicity against two insect species with LD50 values of 18.74 and 32.16 μg/adult, respectively. Among the active compounds, piperitone performed the strongest fumigant toxicity against L. serricorne (LC50 = 1.21 mg/L air) and contact toxicity against T. castaneum (LD50 = 3.16 μg/adult). 1,8-Cineole, limonene and piperitone showed similar fumigant toxicity against T. castaneum with LC50 values of 5.47, 6.21 and 7.12 mg/L air, respectively. Meanwhile, L. serricorne was the most sensitive to 2-tridecanone (LD50 = 5.74 μg/adult) in the progress of contact toxicity assay.
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- 2015
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26. Bioactivity of essential oil from Artemisia stolonifera (Maxim.) Komar. and its main compounds against two stored-product insects.
- Author
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Zhang WJ, Yang K, You CX, Wang Y, Wang CF, Wu Y, Geng ZF, Su Y, Du SS, and Deng ZW
- Subjects
- Animals, Bicyclic Monoterpenes, Bridged Bicyclo Compounds isolation & purification, Bridged Bicyclo Compounds toxicity, Camphor isolation & purification, Camphor toxicity, Chromatography, Gas, Crops, Agricultural parasitology, Cyclohexanols isolation & purification, Cyclohexanols toxicity, Dose-Response Relationship, Drug, Eucalyptol, Flame Ionization, Food Storage, Gas Chromatography-Mass Spectrometry, Monoterpenes isolation & purification, Monoterpenes toxicity, Oils, Volatile analysis, Terpenes isolation & purification, Terpenes toxicity, Artemia chemistry, Insecticides, Oils, Volatile toxicity, Tribolium drug effects
- Abstract
Artemisia stolonifera, a perennial herb, is widely distrbuted in China. The aim of this study was to analyze the essential oil from the aerial parts of Artemisia stolonifera, as well as to evaluate the bioactivity of the oil and its main constituents. The essential oil was analyzed by gas chromatography-flame ionization detector and gas chromatography-mass spectrometry that allowed characterizing 22 compounds. The main components were eucalyptol (32.93%), β-pinene (8.18%), camphor (6.12%) and terpinen-4-ol (6.11%), and obtained from the essential oil after a further isolation. During the contact toxicity tests, the essential oil (LD50 = 8.60 μg/adult) exhibited stronger toxicity against Tribolium castaneum adults than those isolated constituents, however, camphor and terpinen-4-ol showed 1 and 2 times toxicity against Lasioderma serricorne adults than the essential oil (LD50 = 12.68 μg/adult) with LD50 values of 11.30 and 5.42 μg/adult, respectively. In the fumigant toxicity tests, especially on Tribolium castaneum, the essential oil (LC50 = 1.86 mg/L air) showed almost the same level toxicity as positive control, methyl bromide (LC50 = 1.75 mg/L air). Moreover, the essential oil and its four isolated constituents also exhibited strong repellency against two stored-product insects.
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- 2015
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27. Chemical Composition and Bioactivity of Essential Oil of Atalantia guillauminii against Three Species Stored Product Insects.
- Author
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Yang K, You CX, Wang CF, Lei N, Guo SS, Geng ZF, Du SS, Ma P, and Deng ZW
- Subjects
- Animals, Dose-Response Relationship, Drug, Lethal Dose 50, Monoterpenes analysis, Oils, Volatile isolation & purification, Plant Leaves chemistry, Pyrogallol analogs & derivatives, Pyrogallol analysis, Sesquiterpenes analysis, Sesquiterpenes, Eudesmane analysis, Coleoptera drug effects, Crops, Agricultural parasitology, Insect Repellents, Oils, Volatile chemistry, Oils, Volatile toxicity, Rutaceae chemistry
- Abstract
The toxic and repellent activities of the essential oil extracted from the leaves of Atalantia guillauminii Swingle were evaluated against three stored product insects, red flour beetles (Tribolium castaneum), cigarette beetles (Lasioderma serricorne) and booklice (Liposcelis bostrychophila). The essential oil obtained by hydrodistillation was investigated by GC-MS. The main constituents of the essential oil were β-thujene (27.18%), elemicin (15.03%), eudesma-3, 7(11)-diene (9.64%), followed by (-)-4-terpeniol (6.70%) and spathulenol (5.25%). The crude oil showed remarkable contact toxicity against T. castaneum, L. serricorne adults and L. bostrychophila with LD50 values of 17.11, 24.07 µg/adult and 55.83 µg/cm(2) respectively and it also displayed strong fumigant toxicity against T. castaneum, L. serricorne adults with LC50 values of 17.60 and 12.06 mg/L respectively, while weak fumigant toxicity against L. bostrychophila with a LC50 value of 16.75 mg/L. Moreover, the essential oil also exhibited the same level repellency against the three stored product insects, relative to the positive control, DEET. At the same concentrations, the essential oil was more repellent to T. castaneum than to L. serricorne. Thus, the essential oil of A. guillauminii may be potential to be developed as a new natural fumigant/repellent in the control of stored product insects.
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- 2015
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28. Bioactivity and chemical constituents of the essential oil from Dendranthema indicum (L.) Des Moul. against two stored insects.
- Author
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Zhang WJ, You CX, Yang K, Wang Y, Su Y, Geng ZF, Du SS, Wang CF, Deng ZW, and Wang YY
- Subjects
- Animals, Azulenes isolation & purification, Azulenes pharmacology, Cyclohexanols isolation & purification, Drugs, Chinese Herbal, Edible Grain parasitology, Eucalyptol, Food Storage, Gas Chromatography-Mass Spectrometry, Insect Repellents analysis, Insect Repellents pharmacology, Insecticides analysis, Insecticides pharmacology, Monoterpenes isolation & purification, Oils, Volatile isolation & purification, Polycyclic Sesquiterpenes, Sesquiterpenes isolation & purification, Sesquiterpenes, Germacrane isolation & purification, Asteraceae chemistry, Coleoptera drug effects, Oils, Volatile analysis, Oils, Volatile pharmacology
- Abstract
Dendranthema indicum (L.) Des Moul. is a perennial herb commonly used as a traditional Chinese medicine for a long time. In this work, we took Dendranthema indicum as a target plant and two stored insects which include Tribolium castaneum and Stegobium paniceum adults as target insects. Essential oil obtained from Dendranthema indicum was analyzed by gas chromatography-mass spectrometry (GC-MS). A total of 31 components representing 92.44% of the oil were identified and the main compounds were found to be chamazulene (15.93%), β-caryophyllene (13.78%), germacrene D (9.11%), and b-cis-farnesene (6.59%). With a further isolation, three constituents were obtained from the essential oil and identified as chamazulene, β-caryophyllene and eucalyptol. Significantly, in the progress of assay, it showed that the essential oil and chamazulene exhibited stronger insecticidal and repellent activities against Stegobium paniceum than Tribolium castaneum. The results indicate that additional to its traditional use as Chinese medicinal herb, the essential oil of Dendranthema indicum aerial parts and isolated compounds have potential to be developed into natural insecticides or repellents for control of insects in stored grains.
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- 2015
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29. Essential Oil of Amomum maximum Roxb. and Its Bioactivities against Two Stored-Product Insects.
- Author
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Guo SS, You CX, Liang JY, Zhang WJ, Yang K, Geng ZF, Wang CF, Du SS, and Lei N
- Subjects
- Animals, Asia, Southeastern, Bicyclic Monoterpenes, Bridged Bicyclo Compounds analysis, Bridged Bicyclo Compounds isolation & purification, Bridged Bicyclo Compounds pharmacology, Bridged Bicyclo Compounds toxicity, China, Distillation methods, Flame Ionization methods, Fruit chemistry, Fumigation, Gas Chromatography-Mass Spectrometry, Lethal Dose 50, Monoterpenes analysis, Monoterpenes isolation & purification, Monoterpenes pharmacology, Monoterpenes toxicity, Oils, Volatile analysis, Oils, Volatile toxicity, Plant Oils analysis, Plant Oils toxicity, Polycyclic Sesquiterpenes, Sesquiterpenes analysis, Sesquiterpenes isolation & purification, Sesquiterpenes pharmacology, Sesquiterpenes toxicity, Amomum chemistry, Insect Repellents, Insecticides, Oils, Volatile isolation & purification, Oils, Volatile pharmacology, Plant Oils isolation & purification, Plant Oils pharmacology, Tribolium drug effects
- Abstract
Amomum maximum Roxb. is a perennial herb distributed in South China and Southeast Asia. The objective of this work was to analyze the chemical constituents and assess insecticidal and repellent activities of the essential oil from Amomum maximum fruits against Tribolium castaneum (Herbst) and Liposcelis bostrychophila (Badonnel). The essential oil was obtained by hydrodistillation and analyzed by gas chromatography-flame ionization detector and gas chromatography-mass spectrometry. The main components of the essential oil were identified to be β-pinene (23.39%), β-caryophyllene (16.43%), α-pinene (7.55%), sylvestrene (6.61%) and ç-cadinene (4.19%). It was found that the essential oil of A. maximum fruits possessed contact and fumigant toxicities against T. castaneum adults (LD50 = 29.57 μg/adult and LC(50) = 23.09 mg/L air, respectively) and showed contact toxicity against L. bostrychophila (LD(50) = 67.46 μg/cm(2)). Repellency of the crude oil was also evaluated. After 2 h treatment, the essential oil possessed 100% repellency at 78.63 nL/cm(2) against T. castaneum and 84% repellency at 63.17 nL/cm(2) against L. bostrychophila. The results indicated that the essential oil of A. maximum fruits had the potential to be developed as a natural insecticide and repellent for control of T. castaneum and L. bostrychophila.
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- 2015
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30. Chemical constituents and activities of the essential oil from Myristica fragrans against cigarette beetle Lasioderma serricorne.
- Author
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Du SS, Yang K, Wang CF, You CX, Geng ZF, Guo SS, Deng ZW, and Liu ZL
- Subjects
- Animals, Chromatography, Gas, Gas Chromatography-Mass Spectrometry, Coleoptera drug effects, Myristicaceae chemistry, Oils, Volatile chemistry, Oils, Volatile pharmacology
- Abstract
Essential oil extracted from nutmeg seeds (Myristica fragrans Houtt.) by hydrodistillation was subjected to GC/MS and GC analysis. A total of 27 constituents were identified, of which eugenol (19.9%), methylisoeugenol (16.8%), methyleugenol (16.7%), sabinene (11.8%), and terpinen-4-ol (8.5%) were the major components. The essential oil was tested against Lasioderma serricorne for insecticidal and repellent activity, the LD50 value at the end of 24 h exposure period was 19.3 μg/adult. Six active compounds were isolated by bioassay-guided fractionation. They were identified as eugenol (1), methyleugenol (2), methylisoeugenol (3), elemicin (4), myristicin (5), and safrole (6). Among these isolates, 4 showed the strongest contact toxicity against L. serricorne adults with an LD50 value of 9.8 μg/adult. Repellency of crude oil and active compounds were also determined. Compounds 1, 2, 4, and 5 were strongly repellent against the cigarette beetle and exhibited the same level of repellency compared with the positive control, DEET. The results indicate that the essential oil of M. fragrans and its active constituents have potential for development as natural insecticides and repellents to control L. serricorne., (Copyright © 2014 Verlag Helvetica Chimica Acta AG, Zürich.)
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- 2014
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31. Cytotoxic compounds isolated from Murraya tetramera Huang.
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You CX, Yang K, Wang CF, Zhang WJ, Wang Y, Han J, Fan L, Du SS, Geng ZF, and Deng ZW
- Subjects
- Cell Line, Tumor, Humans, Neoplasms pathology, Plant Extracts chemistry, Plant Extracts classification, Drug Screening Assays, Antitumor, Murraya chemistry, Neoplasms drug therapy, Plant Extracts administration & dosage
- Abstract
A new compound and seven known compounds were isolated from Murraya tetramera Huang for the first time, and they were identified with NMR and MS spectral analysis. It was confirmed that the new compound was 10-methoxy-7-methyl-2H-benzo[g]chromen-2-one (3) and the others were β-eudesmol (1), trans-3β-(1-hydroxy-1-methylethyl)-8aβ-methyl-5-methylenedecalin-2-one (2), 5,7-dimethoxy-8-[(Z)-3'-methyl-butan-1',3'-dienyl]coumarin (4), 7-geranyloxy-6-methoxycoumarin (5), 5,7-dimethoxy-8-(3-methyl-2-oxo-butyl)coumarin (6), murrangatin acetate (7) and toddalenone (8). Furthermore, the cytotoxic activity against human lung adenocarcinoma (A549), human hepatocellular carcinoma cells (SMMC-7721), human bladder tumor cells (EJ), human cervical carcinoma cells (HeLa), and human B-lineage acute lymphoblastic leukemia 1 cells (BALL-1) was evaluated for all compounds. It was found that five of them displayed various degrees of cytotoxicity against different testing targets. Compound 1 showed significant cytotoxic activity against the five cell lines (A549, SMMC-7721, EJ, Hela and BALL-1). Compounds 2 and 5 showed significant cytotoxicity against three cell lines (A549, SMMC-7721 and BALL-1). Compound 4 showed significant cytotoxicity against three cell lines (A549, EJ and BALL-1). However, compound 3 only showed fair cytotoxicity against the BALL-1 cell line. The structure-active relationships were investigated as well. These active compounds might be potential lead compounds for the treatment of cancer.
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- 2014
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32. Bioactivity of essential oil of Artemisia argyi Lévl. et Van. and its main compounds against Lasioderma serricorne.
- Author
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Zhang WJ, You CX, Yang K, Chen R, Wang Y, Wu Y, Geng ZF, Chen HP, Jiang HY, Su Y, Lei N, Ma P, Du SS, and Deng ZW
- Subjects
- Animals, Dose-Response Relationship, Drug, Lethal Dose 50, Oils, Volatile chemistry, Artemisia chemistry, Coleoptera drug effects, Insecticides chemistry, Oils, Volatile isolation & purification, Oils, Volatile pharmacology
- Abstract
Artemisia argyi Lévl. et Van., a perennial herb with a strong volatile odor, is widely distrbuted in the world. Essential oil obtained from Artemisia argyi was analyzed by gas chromatography-mass spectrometry (GC-MS). A total of 32 components representing 91.74% of the total oil were identified and the main compounds in the oil were found to be eucalyptol (22.03%), β-pinene (14.53%), β-caryophyllene (9.24%) and (-)-camphor (5.45%). With a further isolation, four active constituents were obtained from the essential oil and identified as eucalyptol, β-pinene, β-caryophyllene and camphor. The essential oil and the four isolated compounds exhibited potential bioactivity against Lasioderma serricorne adults. In the progress of assay, it showed that the essential oil, camphor, eucalyptol, β-caryophyllene and β-pinene exhibited strong contact toxicity against L. serricorne adults with LD50 values of 6.42, 11.30, 15.58, 35.52, and 65.55 μg/adult, respectively. During the fumigant toxicity test, the essential oil, eucalyptol and camphor showed stronger fumigant toxicity against L. serricorne adults than β-pinene (LC50 = 29.03 mg/L air) with LC50 values of 8.04, 5.18 and 2.91 mg/L air. Moreover, the essential oil, eucalyptol, β-pinene and camphor also exhibited the strong repellency against L. serricorne adults, while, β-caryophyllene exhibited attracting activity relative to the positive control, DEET. The study revealed that the bioactivity properties of the essential oil can be attributed to the synergistic effects of its diverse major and minor components. The results indicate that the essential oil of A. argyi and the isolated compounds have potential to be developed into natural insecticides, fumigants or repellents in controlling insects in stored grains and traditional Chinese medicinal materials.
- Published
- 2014
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33. Composition and repellency of the essential oils of Evodia calcicola Chun ex Huang and Evodia trichotoma (Lour.) Pierre against three stored product insects.
- Author
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Yang K, You CX, Wang CF, Guo SS, Li YP, Wu Y, Geng ZF, Deng ZW, and Du SS
- Subjects
- Animals, Distillation methods, Oils, Volatile chemistry, Oils, Volatile isolation & purification, Coleoptera drug effects, Evodia chemistry, Insect Repellents, Insecticides, Oils, Volatile pharmacology, Phthiraptera drug effects, Plant Leaves chemistry, Tribolium drug effects
- Abstract
During our screening program for agrochemicals from Chinese medicinal herbs and wild plants, the essential oils of Evodia calcicola and Evodia trichotoma leaves were found to possess strong repellency against the red flour beetle Tribolium castaneum adults, the cigarette beetle Lasioderma serricorne adults and the booklouse Liposcelis bostrychophila. The two essential oils obtained by hydrodistillation were investigated by GC-MS. The main components of E. calcicola essential oil were identified to be (-)-β-pinene (44.02%), β-phellandrene (20.93%), ocimene (16.49%), and D-limonene (9.87%). While the main components of the essential oil of E. trichotoma were D-limonene (69.55%), 1R-a-pinene (11.48%), caryophyllene (2.80%) and spathulenol (2.24%). Data showed that T. castaneum was the most sensitive than other two stored product insects. Compared with the positive control, DEET (N, N-diethyl-3- methylbenzamide), the two essential oils showed the same level repellency against the red flour beetle. However, the essential oil of E. trichotoma showed the same level repellency against the cigarette beetle, while E. calcicola essential oil possessed the less level repellency against L. serricorne, relative to the positive control, DEET. Moreover, the two crude oils also exhibited strong repellency against L. bostrychophila, but lesser level repellency than the positive control, DEET. Thus, the essential oils of E. calcicola and E. trichotoma may be potential to be developed as a new natural repellent in the control of stored product insects.
- Published
- 2014
- Full Text
- View/download PDF
34. Chemical constituents and insecticidal activities of the essential oil from Amomum tsaoko against two stored-product insects.
- Author
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Wang Y, You CX, Wang CF, Yang K, Chen R, Zhang WJ, Du SS, Geng ZF, and Deng ZW
- Subjects
- Animals, Cyclohexanols isolation & purification, Cyclohexanols pharmacology, Cyclohexenes isolation & purification, Cyclohexenes pharmacology, Edible Grain parasitology, Eucalyptol, Food Parasitology, Food Storage, Gas Chromatography-Mass Spectrometry, Insecticides isolation & purification, Lethal Dose 50, Limonene, Monoterpenes isolation & purification, Monoterpenes pharmacology, Oils, Volatile isolation & purification, Terpenes isolation & purification, Terpenes pharmacology, Tribolium, Amomum chemistry, Coleoptera drug effects, Insecticides chemistry, Insecticides pharmacology, Oils, Volatile chemistry, Oils, Volatile pharmacology
- Abstract
The aim of this research was to determine the chemical constituents and toxicities of the essential oil derived from Amomum tsaoko Crevost et Lemarie fruits against Tribolium castaneum (Herbst) and Lasioderma serricorne (Fabricius). Essential oil of A. tsaoko was obtained from hydrodistillation and was investigated by gas chromatography-mass spectrometry (GC-MS). GC-MS analysis of the essential oil resulted in the identification of 43 components, of which eucalyptol (23.87%), limonene (22.77%), 2-isopropyltoluene (6.66%) and undecane (5.74%) were the major components. With a further isolation, two active constituents were obtained from the essential oil and identified as eucalyptol and limonene. The essential oil and the two isolated compounds exhibited potential insecticidal activities against two storedproduct insects. Limonene showed pronounced contact toxicity against both insect species (LD50 = 14.97 μg/adult for T. castaneum; 13.66 μg/adult for L. serricorne) and was more toxic than eucalyptol (LD50 = 18.83 μg/adult for T. castaneum; 15.58 μg/adult for L. serricorne). The essential oil acting against the two species of insects showed LD50 values of 16.52 and 6.14 μg/adult, respectively. Eucalyptol also possessed strong fumigant toxicity against both insect species (LC50 = 5.47 mg/L air for T. castaneum; 5.18 mg/L air for L. serricorne) and was more toxic than limonene (LC50 = 6.21 mg/L air for T. castaneum; 14.07 mg/L air for L. serricorne), while the crude essential oil acting against the two species of insects showed LC50 values of 5.85 and 8.70 mg/L air, respectively. These results suggested that the essential oil of A. tsaoko and the two compounds may be used in grain storage to combat insect pests.
- Published
- 2014
- Full Text
- View/download PDF
35. Cytotoxic constituents from the stems of Clausena lansium (Lour.) Skeels.
- Author
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Jiang HY, Wang CF, Fan L, Yang K, Feng JB, Geng ZF, Xu J, Deng ZW, Du SS, and Yin HB
- Subjects
- Aldehydes isolation & purification, Antineoplastic Agents, Phytogenic isolation & purification, Carbazoles isolation & purification, Doxorubicin pharmacology, Drug Screening Assays, Antitumor, HeLa Cells, Heterocyclic Compounds, 3-Ring isolation & purification, Humans, Inhibitory Concentration 50, K562 Cells, Plant Extracts isolation & purification, Aldehydes pharmacology, Antineoplastic Agents, Phytogenic pharmacology, Carbazoles pharmacology, Clausena chemistry, Heterocyclic Compounds, 3-Ring pharmacology, Plant Extracts pharmacology, Plant Stems chemistry
- Abstract
Six compounds were isolated from the stems of Clausena lansium (Lour.) Skeels by repeated sillica gel column chromatography. Their chemical structures were elucidated on the basic of physicochemical and spectroscopic data. Among them, 8-geranyloxypsolaren (3) and 2-methoxy-1-(3-methyl-buten-1-yl)-9H-carbazole-3-carbaldehyde (6) were isolated for the first time from this plant. These compounds were screened for cytotoxicity in human cervical cancer (Hela), leukemia (K562), lung cancer (A549), non-small lung carcinoma (H1299) and liver cancer (SMMC-7721). Within the series of cytotoxic tests, compounds 4-6 displayed potent cytotoxic activity against H1299 and SMMC-7721, with the IC₅₀ values of 6.19 to 26.84 μg/mL.
- Published
- 2013
- Full Text
- View/download PDF
36. Feeding deterrents against two grain storage insects from Euphorbia fischeriana.
- Author
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Geng ZF, Liu ZL, Wang CF, Liu QZ, Shen SM, Liu ZM, Du SS, and Deng ZW
- Subjects
- Animals, Diterpenes chemistry, Magnetic Resonance Spectroscopy, Molecular Structure, Pesticides chemistry, Coleoptera physiology, Diterpenes pharmacology, Euphorbia parasitology, Feeding Behavior drug effects, Pesticides pharmacology
- Abstract
The screening of several Chinese medicinal herbs for insecticidal principles showed that Euphorbia fischeriana roots possessed significant feeding deterrent activity against two stored-product insects (Tribolium castaneum and Sitophilus zeamais). From ethanol extract, four feeding deterrents were isolated by bioassay-guided fractionation. The compounds were identified as jolkinolide B, 12-deoxyphorbol 13-(9Z)-octadecenoate 20-acetate, 17-hydroxyjolkinolide A and B on the basis of their phytochemical and spectral data. Jolkinolide B and 17-hydroxyjolkinolide B possessed strong feeding deterrent activities against S. zeamais (EC₅₀ = 342.1 and 543.9 ppm, respectively) and T. castaneum adults (E₅₀ = 361.4 and 551.5 ppm, respectively). 17-Hydroxyjolkinolide A and 12-deoxyphorbol 13-(9Z)-octadecenoate 20-acetate A also exhibited feeding deterrent activity against the two grain storage insects with EC₅₀ values of 631.9 and 884.3 ppm for S. zeamais and 656.5 and 1058.4 ppm for T. castaneum adults.
- Published
- 2011
- Full Text
- View/download PDF
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