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1.
Org Lett ; 25(22): 4150-4155, 2023 Jun 09.
Article in English | MEDLINE | ID: mdl-37252906

ABSTRACT

A convenient and efficient approach was developed to synthesize α-Kdo O-glycosides based on the Tf2O/(p-Tol)2SO preactivation strategy using peracetylated Kdo thioglycoside as a donor. Under the optimized reaction conditions, several O-glycoside products, including α-(2 → 1)-, α-(2 → 2)-, α-(2 → 3)-, and α-(2 → 6)-Kdo products, were stereoselectively synthesized in high yields. Remarkably, a series of aromatic α-Kdo O-glycosides were first and successfully constructed in high yields. An SN2-like mechanism was revealed by DFT calculations and experimental results.


Subject(s)
Cardiac Glycosides , Glycosides , Glycosylation , Sugar Acids , Lipopolysaccharides
2.
ACS Omega ; 6(39): 25497-25505, 2021 Oct 05.
Article in English | MEDLINE | ID: mdl-34632207

ABSTRACT

By implementing NMR, inductively coupled plasma-atomic emission spectrometry (ICP-AES), and the UV-vis spectroscopic techniques, metabolites, mineral elements, and antioxidant activities (DPPH) of Peganum harmala L. samples from Manasi and Fuhai of Xinjiang were studied in this research to investigate the geographical environment impact at the molecular level. First of all, partial least squares discriminant analysis was conducted to explore differential endogenous metabolites. A total of 18 metabolites were identified, and 14 mineral element contents were calculated quantitatively, which displayed diverse changing trends from these two origins. Valine, succinic acid, betaine, sucrose, and vasicine exhibited significant differences between these two groups as well as mineral nutrient profiles (Mg, Cu, N, K, Na, P, Zn, C) and DPPH antioxidant activities (EC50). The obvious different characteristics of chemical components and antioxidant activities in these two groups were further verified by heat map cluster analysis. Pearson correlation analysis also revealed the remarkable relationship of chemical components and antioxidant activities, which are strongly associated with the regional environment. This study showed that the combination of methodologies proposed will be highly useful in evaluating the environmental variation and diversity in terrestrial ecosystems.

3.
Nat Prod Res ; 34(18): 2595-2601, 2020 Sep.
Article in English | MEDLINE | ID: mdl-30623674

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.


Subject(s)
Cyclooctanes/chemistry , Feeding Behavior/drug effects , Lignans/chemistry , Plant Stems/chemistry , Schisandra/chemistry , Tribolium , 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 , Tribolium/drug effects , Triterpenes/analysis , Triterpenes/isolation & purification
4.
Ecotoxicol Environ Saf ; 190: 110106, 2020 Mar 01.
Article in English | MEDLINE | ID: mdl-31877546

ABSTRACT

In this work, the essential oil (EO) and supercritical CO2 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.


Subject(s)
Bicyclic Monoterpenes/chemistry , Camphanes/chemistry , Insect Repellents/toxicity , Valerianaceae , Animals , Coleoptera , Gas Chromatography-Mass Spectrometry , Insect Repellents/analysis , Insecta , Insecticides/analysis , Oils, Volatile/chemistry
5.
Environ Sci Pollut Res Int ; 26(24): 24988-24997, 2019 Aug.
Article in English | MEDLINE | ID: mdl-31240663

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 (LD50 = 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.


Subject(s)
Insect Repellents/pharmacology , Insecticides/analysis , Monoterpenes/chemistry , Oils, Volatile/chemistry , Terpenes/chemistry , Zanthoxylum/chemistry , Acyclic Monoterpenes , Animals , Coleoptera/drug effects , Gas Chromatography-Mass Spectrometry , Insect Repellents/chemistry , Insecticides/chemistry , Lethal Dose 50 , Monoterpenes/analysis , Oxidation-Reduction , Tribolium/chemistry
6.
Ecotoxicol Environ Saf ; 169: 807-813, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30597779

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/cm2 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 (ß-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 ß-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, N­diethyl­3­methylbenzamide), 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.


Subject(s)
Atractylodes/chemistry , Drugs, Chinese Herbal/chemistry , Insecticides , Tribolium , Animals , Gas Chromatography-Mass Spectrometry , Insect Repellents/chemistry , Insect Repellents/isolation & purification , Insecticides/chemistry , Insecticides/isolation & purification , Oils, Volatile , Sesquiterpenes/chemistry , Sesquiterpenes/isolation & purification
7.
J Anal Methods Chem ; 2018: 6532789, 2018.
Article in English | MEDLINE | ID: mdl-30581649

ABSTRACT

A nuclear magnetic resonance- (NMR-) based metabolomics method was used to identify differential metabolites of methanol extracts obtained from six parts of Peganum harmala L. (P. harmala), namely, the root, stem, leaf, flower, testa, and seed. Two multivariate statistical analysis methods, principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA), were combined to clearly distinguish among the P. harmala samples from the six different parts. Eleven differential components were screened by the PLS-DA loading plot, and the relative contents were calculated by univariate analysis of variance. Chemometric results showed significant differences in the metabolites of the different parts of P. harmala. The seeds contained large amounts of harmaline, harmine, and vasicine compared to other organs. The acetic acid, proline, lysine, and sucrose contents of the roots were significantly higher than those of the other parts. In the testa, the vasicine, asparagine, choline, and 4-hydroxyisoleucine contents were clearly dominant. The obtained data revealed the distribution characteristics of the metabolomes of the different P. harmala parts and provided fundamental knowledge for the rational development of its medicinal parts.

8.
R Soc Open Sci ; 5(7): 171722, 2018 Jul.
Article in English | MEDLINE | ID: mdl-30109044

ABSTRACT

Xerophytes play an active role in preventing soil denudation and desertification in arid and semi-arid areas. Peganum harmala L. (Zygophyllaceae family), a seasonally growing, poisonous and drought-tolerant plant, is widely distributed in the Xinjiang Uygur Autonomous Region and used as a traditional herbal medicine as well as, in winter, a fodder source. Previous research has focused on the pharmacological activity of isolated compounds and stress responses to growth environments. However, the metabolic profile of P. harmala and variations in its metabolites, including medicinally active and stress resistance components, have not been illustrated during different growth stages. Here, we collected plant samples in May, August, October and December. We determined the metabolic composition of methanol extracts using NMR spectroscopy, and comparisons of four growth stages were accomplished by applying statistical analysis. The results showed that vasicine, choline and sucrose were significantly elevated in samples harvested in May. Significantly higher amounts of betaine, lysine, 4-hydroxyisoleucine and proline were found in samples collected in August than in samples collected in other months, and the concentrations of phosphorylcholine, glucose, acetic acid and vasicinone were highest in December. The relationships between differential biomarkers and plant physiological states affected by diverse growth environmental factors were discussed. Our result deepened the understanding of metabolic mechanisms in plant development and confirmed the advantage of using NMR-based metabolomic treatments in quality evaluation when P. harmala is used for different purposes.

9.
Molecules ; 23(9)2018 Aug 24.
Article in English | MEDLINE | ID: mdl-30149520

ABSTRACT

Toxic and repellent effects of the essential oil from Asarum heterotropoides Fr. Schmidt var. mandshuricum (Maxim.) Kitag. were evaluated against Lasioderma serricorne and Liposcelis bostrychophila. The essential oils (EOs) from roots (ER) and leaves (EL) of A. heterotropoides were obtained separately by hydrodistillation and characterized by gas chromatography-mass spectrometry (GC-MS) analysis. Major components of ER and EL included methyleugenol, safrole, and 3,5-dimethoxytoluene. Both ER and EL of A. heterotropoides showed certain toxicity and repellency against L. serricorne and L. bostrychophila. 3,5-Dimethoxytoluene, methyleugenol, and safrole were strongly toxic via fumigation to L. serricorne (LC50 = 4.99, 10.82, and 18.93 mg/L air, respectively). Safrole and 3,5-dimethoxytoluene possessed significant fumigant toxicity against L. bostrychophila (LC50 = 0.83 and 0.91 mg/L air, respectively). The three compounds all exhibited potent contact toxicity against the two insect species. Here, the EL of A. heterotropoides was confirmed to have certain toxicity and repellency against stored product insects, providing a novel idea for the comprehensive use of plant resources.


Subject(s)
Asarum/chemistry , Coleoptera/drug effects , Plant Extracts/chemistry , Plant Extracts/pharmacology , Propanols/chemistry , Propanols/pharmacology , Volatile Organic Compounds/chemistry , Volatile Organic Compounds/pharmacology , Animals , Gas Chromatography-Mass Spectrometry , Insect Repellents/chemistry , Insect Repellents/pharmacology , Insecta/drug effects , Oils, Volatile/chemistry , Phytochemicals/chemistry , Plant Roots/chemistry
10.
J Oleo Sci ; 67(8): 1027-1034, 2018 Aug 01.
Article in English | MEDLINE | ID: mdl-30012895

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%), ß-caryophyllene (23.1%), ß-elemene (14.5%), and ß-cubebene (4.7%), while the main components of the E. rutaecarpa EO are α-pinene (39.4%), ß-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.


Subject(s)
Coleoptera/drug effects , Evodia/chemistry , Insect Repellents , Oils, Volatile/chemistry , Oils, Volatile/toxicity , Plant Leaves/chemistry , Tribolium/drug effects , 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
11.
Ecotoxicol Environ Saf ; 160: 342-348, 2018 Sep 30.
Article in English | MEDLINE | ID: mdl-29857238

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%), ß-pinene (11.5%), 3-carene (9.6%), caryophyllene oxide (8.7%) and ß-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.


Subject(s)
Evodia , Insect Repellents/toxicity , Insecticides/toxicity , Monoterpenes/toxicity , Neoptera/drug effects , Oils, Volatile/toxicity , Phytochemicals/toxicity , 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
12.
Environ Sci Pollut Res Int ; 25(22): 22236-22243, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29804253

ABSTRACT

The extract from Cinnamomum cassia Presl bark was obtained with supercritical CO2 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.


Subject(s)
Cinnamomum aromaticum/chemistry , Insect Repellents/analysis , Insecticides/analysis , Tribolium , Animals , Carbon Dioxide , Chromatography, Supercritical Fluid , Gas Chromatography-Mass Spectrometry , Plant Bark/chemistry , Plant Extracts/chemistry
13.
Molecules ; 23(3)2018 Mar 09.
Article in English | MEDLINE | ID: mdl-29522428

ABSTRACT

The speciation of a methanolic extract of Zanthoxylum armatum stem bark has enabled the isolation and characterization of 11 known lignans. Among them, five compounds (6, 8-11) are reported in this plant for the first time. All of the chemical structures were elucidated on the basis of NMR spectral analysis. Additionally, their antifeedant activities against Tribolium castaneum were evaluated scientifically. Among them, asarinin (1), with an EC50 of 25.64 ppm, exhibited a much stronger antifeedant activity than the positive control, toosendanin (EC50 = 71.69 ppm). Moreover, fargesin (2), horsfieldin (3), and magnolone (10), with EC50 values of 63.24, 68.39, and 78.37 ppm, showed almost the same antifeedant activity as the positive control. From the perspective of structure-effectiveness relationship, compounds with the chemical group of methylenedioxy exhibited higher antifeedant activities and have potential to be developed into novel antifeedants or potential lead compounds to protect food and crops in storage.


Subject(s)
Lignans/chemistry , Lignans/pharmacology , Plant Bark/chemistry , Plant Extracts/chemistry , Plant Extracts/pharmacology , Plant Stems/chemistry , Tribolium/drug effects , Zanthoxylum/chemistry , Animals , Molecular Structure , Phytochemicals/chemistry
14.
Nat Prod Res ; 32(10): 1234-1238, 2018 May.
Article in English | MEDLINE | ID: mdl-28532258

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 LC50 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.


Subject(s)
Artemisia/chemistry , Insect Repellents/pharmacology , Oils, Volatile/chemistry , Phthiraptera/drug effects , Tribolium/drug effects , Animals , Cyclohexane Monoterpenes , Cyclohexenes/pharmacology , Food Storage , Insect Control/methods , Insect Repellents/chemistry , Limonene , Terpenes/pharmacology
15.
Molecules ; 22(8)2017 Aug 20.
Article in English | MEDLINE | ID: mdl-28825643

ABSTRACT

Sixteen compounds were isolated from the leaves and stems of Murrayatetramera 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-1ß,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.


Subject(s)
Insect Repellents/chemistry , Insect Repellents/pharmacology , Murraya/chemistry , Plant Extracts/chemistry , Tribolium/drug effects , Animals , Magnetic Resonance Spectroscopy , Molecular Structure
16.
Molecules ; 22(4)2017 Apr 18.
Article in English | MEDLINE | ID: mdl-28420198

ABSTRACT

Alpinia officinarum has been confirmed to possess bioactivities against some pests. In this work, a sample was obtained from A. officinarum rhizomes by supercritical fluid CO2 extraction (SFE). According to GC-MS analysis, the main chemical components for SFE-sample included benzylacetone (26.77%), 1,7-diphenyl-5-hydroxy-3-heptanone (17.78%), guaiacylacetone (10.03%) and benzenepropanal (7.42%). The essential oil of A. officinarum rhizomes (LD50 = 20.71 µg/adult) exhibited more contact toxicity than SFE extract (LD50 = 82.72 µg/adult) against Tribolium castaneum. From SFE extracts, one new compound, 1-phenyl-4-(16,17-dimethyl-9,13-octadiene)-5-isopentenyl-7-(4"-methoxyl-3"-hydroxyl-phenyl)-3-heptanone (3), together with five known compounds identified as 5-hydroxy-1,7-diphenyl-3-heptanone (1), 1,7-diphenyl-4-hepten-3-one (2), galangin (4), galangin-3-methyl ether (5) and pinocembrin (6), were isolated and their feeding deterrent activities against T. castaneum adults were assessed. It was found that compounds 1-6 had feeding deterrent activities against T. castaneum with feeding deterrent indices of 18.21%, 18.94%, 19.79%, 26.99%, 20.34%, and 35.81%, respectively, at the concentration of 1500 ppm. Hence, the essential oil and SFE extracts/compounds of A. officinarum rhizomes represent promising alternatives in the control of T. castaneum adults.


Subject(s)
Alpinia/chemistry , Insecticides/chemistry , Insecticides/pharmacology , Plant Extracts/chemistry , Plant Extracts/pharmacology , Tribolium/drug effects , Animals , Gas Chromatography-Mass Spectrometry , Magnetic Resonance Spectroscopy , Molecular Structure , Phytochemicals/chemistry
17.
Nat Prod Res ; 31(10): 1201-1204, 2017 May.
Article in English | MEDLINE | ID: mdl-27563800

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 ß-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.


Subject(s)
Insect Repellents/pharmacology , Oils, Volatile/pharmacology , Rutaceae/chemistry , Allylbenzene Derivatives , Animals , Anisoles/pharmacology , Oils, Volatile/analysis , Tribolium
18.
Nat Prod Res ; 31(7): 791-796, 2017 Apr.
Article in English | MEDLINE | ID: mdl-27739326

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.


Subject(s)
Rutaceae/chemistry , Amides/chemistry , Magnetic Resonance Spectroscopy/methods , Mass Spectrometry , Molecular Structure , Sulfonamides/chemistry , Sulfur/chemistry
19.
Int J Mol Sci ; 17(11)2016 Nov 04.
Article in English | MEDLINE | ID: mdl-27827929

ABSTRACT

To investigate the chemical composition and insecticidal activity of the essential oils of certain Chinese medicinal herbs and spices, the essential oils were extracted from the stem barks, leaves, and fruits of Cinnamomum camphora (L.) Presl, which were found to possess strong fumigant toxicity against Tribolium castaneum and Lasioderma serricorne adults. The essential oils of the plants were extracted by the method of steam distillation using a Clavenger apparatus. Their composition was determined by gas chromatography/mass spectrometric (GC-MS) analyses (HP-5MS column), and their insecticidal activity was measured by seal-spaced fumigation. D-camphor (51.3%), 1,8-cineole (4.3%), and α-terpineol (3.8%), while D-camphor (28.1%), linalool (22.9%), and 1,8-cineole (5.3%) were the main constituents of its fruits. The essential oils of the C. camphora all showed fumigant and contact toxicity. Other compounds exhibited various levels of bioactivities. The results indicate that the essential oils of C. camphora and its individual compounds can be considered a natural resource for the two stored-product insect management.


Subject(s)
Cinnamomum camphora/chemistry , Insecticides/chemistry , Monoterpenes/chemistry , Oils, Volatile/chemistry , Acyclic Monoterpenes , Animals , Camphor/chemistry , Camphor/isolation & purification , Coleoptera , Cyclohexane Monoterpenes , Cyclohexenes/chemistry , Cyclohexenes/isolation & purification , Fruit/chemistry , Gas Chromatography-Mass Spectrometry , Insecticides/isolation & purification , Lethal Dose 50 , Liquid-Liquid Extraction/methods , Monoterpenes/isolation & purification , Oils, Volatile/isolation & purification , Plant Bark/chemistry , Plant Extracts/chemistry , Plant Leaves/chemistry , Tribolium
20.
J Oleo Sci ; 65(10): 871-879, 2016 Oct 01.
Article in English | MEDLINE | ID: mdl-27628733

ABSTRACT

Two essential oil samples were obtained from the pericarp of Zanthoxylum bungeanum with the methods of hydrodistillation (HD) and supercritical fluid CO2 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.


Subject(s)
Coleoptera/drug effects , Insect Repellents , Insecticides , Plant Oils , Zanthoxylum/chemistry , Animals , Chromatography, Supercritical Fluid , Distillation , Fatty Acids/analysis , Fatty Acids/isolation & purification , Gas Chromatography-Mass Spectrometry , Insect Repellents/analysis , Insect Repellents/isolation & purification , Insecticides/analysis , Insecticides/isolation & purification , Monoterpenes/analysis , Monoterpenes/isolation & purification , Plant Oils/analysis , Plant Oils/isolation & purification , Sesquiterpenes/analysis , Sesquiterpenes/isolation & purification
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