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Piperidinyl amides with insecticidal activity from the maritime plant Otanthus maritimus.

Two new piperidine amides, N-[(2E,4E,8Z)-tetradecatrienoyl]piperidine (1) and N-[(2E,4E,8Z,11Z)-tetradecatetrenoyl]piperidine (2), along with the known metabolites N-[(2E,4E)-tetradecadienoyl]piperidine (3), N-isobutyl-(2E,4E,)-tetradecadienamide (4), N-isobutyl-(2E,4E,8Z)-tetradecatrienamide (5), N-isobutyl-(2E,4E,8Z,11Z)-tetradecatetraenamide (6), sesamine (7), pinoresinol (8), and espeletone (9), were isolated from the dichloromethane/methanol extracts of the plant Otanthus maritimus Hoffman & Link collected from coastal areas in Greece. Pinoresinol (8) and espeletone (9) are reported for the first time as metabolites of O. maritimus. The structures of the new natural products were elucidated by interpretation of their NMR and high-resolution mass spectral measurements. The insecticidal properties of the crude extracts, essential oil, and isolated metabolites 1-9 were evaluated on Crematogaster scutellaris (Olivier) ants and Reticulitermes balkanensis (Clement) termites, showing significant levels of activity.

Alkenes↗

Fumigant activity of plant essential oils and components from garlic (Allium sativum) and clove bud (Eugenia caryophyllata) oils against the Japanese termite (Reticulitermes speratus Kolbe).

Plant essential oils from 29 plant species were tested for their insecticidal activities against the Japanese termite, Reticulitermes speratus Kolbe, using a fumigation bioassay. Responses varied with plant material, exposure time, and concentration. Good insecticidal activity against the Japanese termite was achived with essential oils of Melaleuca dissitiflora, Melaleuca uncinata, Eucalyptus citriodora, Eucalyptus polybractea, Eucalyptus radiata, Eucalyptus dives, Eucalyptus globulus, Orixa japonica, Cinnamomum cassia, Allium cepa, Illicium verum, Evodia officinalis, Schizonepeta tenuifolia, Cacalia roborowskii, Juniperus chinensis var. horizontalis, Juniperus chinensis var. kaizuka, clove bud, and garlic applied at 7.6 microL/L of air. Over 90% mortality after 3 days was achieved with O. japonica essential oil at 3.5 microL/L of air. E. citriodora, C. cassia, A. cepa, I. verum, S. tenuifolia, C. roborowskii, clove bud, and garlic oils at 3.5 microL/L of air were highly toxic 1 day after treatment. At 2.0 microL/L of air concentration, essential oils of I. verum, C. roborowskik, S. tenuifolia, A. cepa, clove bud, and garlic gave 100% mortality within 2 days of treatment. Clove bud and garlic oils showed the most potent antitermitic activity among the plant essential oils. Garlic and clove bud oils produced 100% mortality at 0.5 microL/L of air, but this decreased to 42 and 67% after 3 days of treatment at 0.25 microL/L of air, respectively. Analysis by gas chromatography-mass spectrometry led to the identification of three major compounds from garlic oil and two from clove bud oils. These five compounds from two essential oils were tested individually for their insecticidal activities against Japanese termites. Responses varied with compound and dose. Diallyl trisulfide was the most toxic, followed by diallyl disulfide, eugenol, diallyl sulfide, and beta-caryophyllene. The essential oils described herein merit further study as potential fumigants for termite control.

Animals↗

Synthetic approach toward the total synthesis of kempane diterpenes via transannular Diels-Alder strategy.

Total syntheses of two new (+/-)-kempane derivatives 30 and 47 were achieved with transannular Diels-Alder reaction (TADA) serving as the key step for the stereoselective formation of tricyclic [6.6.5] system 3. This synthetic approach also reveals that the geometry of the C3 group of such a tricyclic system plays an important role for the formation of the seven-membered kempane skeleton.

Animals↗

Synthetic approach to exo-endo cross-conjugated cyclohexadienones and its application to the syntheses of dehydrobrachylaenolide, isodehydrochamaecynone, and trans-isodehydrochamaecynone.

Methodology for synthesis of exo-endo cross-conjugated dienones with trans- and cis-decalin systems has been reported. Bromination of the silyl enol ether of alpha'-methyl alpha,beta-unsaturated ketones with PTAB and successive dehydrobromination of the resulting alpha'-bromo-alpha'-methyl alpha,beta-unsaturated ketones under three conditions (DBU/PhH; TBAF/THF; Li(2)CO(3), LiBr/DMF) gave the desired exo-endo cross-conjugated dienones in good yield. This method was applied to the syntheses of dehydrobrachylaenolide (1), isodehydrochamaecynone (5c), and trans-isodehydrochamaecynone (11) starting from tuberiferine (7), chamaecynone (5a), and trans-chamaecynone (9). Eudesmanolides possessing an alpha-methylene gamma-lactone moiety, i.e., 1, 7, and 13, exhibited significant inhibitory activity toward the induction of the intercellular adhesion molecule-1 (ICAM-1). Compound 1 showed greater activity than 7 and 13. All compounds possessing an ethynyl group, 5d, 9, 11, and 14, showed the same degree of termiticidal activity, and the exo-endo cross-conjugated dienone structure in 11 had no influence on the activity.

Animals↗

Trinervitene diterpenes from soldiers of two Nasutitermes species from French Guyana.

Methanolic extracts of soldiers of Nasutitermes guayanae and N. surinamensis have been shown to contain complex mixtures of diterpenes and monoterpenes. Eighteen diterpenes have been isolated and identified; twelve of them are previously known nasute termite diterpenes, while six are new trinervitene diterpenes. 2alpha,9beta-Dihydroxy-3beta,8beta-oxido-1(15)-trinervitene has been isolated from N. guayanae, while 3alpha,14alpha-diacetoxy-2beta-hydroxy-1(15),8(19),9-trinervitatriene, 14alpha-acetoxy-2beta,3alpha-dihydroxy-1(15),8(19),9-trinervitatriene, 2beta,3alpha-diacetoxy-11beta,14alpha-dihydroxy-1(15),8(19)-trinervitadiene, 9alpha,14alpha-diacetoxy-2beta,3alpha-dihydroxy-1(15),8(19)-trinervitadiene, and 2beta,9alpha,14alpha-triacetoxy-3alpha-hydroxy-1(15),8(19)-trinervitadiene have been isolated from N. surinamensis. Their structures were determined on the basis of their spectroscopic properties.

Animals↗

The first total synthesis of (-) and (+)-2-hydroxy-24-oxooctacosanolide using an effective lactonization.

[structure: see text] An effective method for the total synthesis of 2-hydroxy-24-oxooctacosanolide, a defensive salivary secretion of the African termite Pseudacanthotermes spiniger, has been developed. The key lactonization to form a 29-membered ring lactone core is performed using 2-methyl-6-nitrobenzoic anhydride with a catalytic amount of 4-(dimethylamino)pyridine N-oxide.

Animals↗

Influence of minerals on the aetiology of geophagia in periurban dairy cattle in the derived savannah of Nigeria.

The aetiology of geophagia in periurban dairy cattle in Nigeria was assessed in relation to the mineral status of the serum, the herbage consumed, and the soil from where the herbage was consumed. The study was carried out using nine herds in the derived savannah zone during both the wet and dry seasons. Generally, the Na, Ca, Fe, Zn and Cu levels in the samples were adequate. However, the forages were low in Ca and the serum was deficient in P. Forage, soil and termite hill samples were also deficient in P. The low levels of P in the soil and termite hill samples showed that the consumption of sand by the cattle did not have any positive impact on their P intake. A seasonal effect was apparent (p < 0.05) on the serum Na+, PO4(3-), Cu2+ and Fe2+ concentrations but not on Ca2+ and Zn2+ concentrations. A seasonal effect was also significant (p < 0.05) on the minerals in the forage. There were also seasonal differences in most of the soil and termite hill minerals. Most samples had higher (p < 0.05) mineral levels in the dry season. Herd size and farming activity had no apparent influence on the aetiology of geophagia as they did not affect (p > 0.05) the concentration of P in the serum, the reported cause of geophagia. Geophagia is probably caused by a marginal level of P in the serum and low levels in the forage and soil. Experimental trials will be required to confirm these observations.

Animal Feed↗

Thin-layer chromatography assessing feeding stimulation by labial gland secretion compared to synthetic chemicals in the subterranean termite Reticulitermes santonensis.

The labial gland of the French subterranean termite Reticulitermes santonensis De Feytaud contains a polar, heat-resistent, and persistent chemical signal that is released onto the food during food exploitation and stimulates feeding in nestmates. Separation of the labial gland secretion by thin-layer chromatography on cellulose plates revealed that the secretion contains components with reducing and amino groups. In feeding bioassays conducted on the cellulose plate after TLC, termites preferred the area between Rf 0.46 and 0.88 (biologically active zone) for feeding, indicating the location of the feeding-stimulating signal. Thirty-five synthetic chemicals with similar chemical properties as the feeding-stimulating signal were analyzed with TLC. None of them covered the biologically active zone. Therefore, all chemical classes tested, such as sugars, amino acids, and salts, are unlikely as possible sources for the signal structure. In feeding choice tests with synthetic chemicals, termites showed clear feeding preference only for sugarlike components with physiologically excessive concentrations of 10 mmol and 100 mmol. Amino acids induced only light feeding preference. The intensity of feeding stimulation by the natural signal from the labial gland as compared to synthetic phagostimulants is discussed.

Animals↗

Survey of termite-inhabited soil and mosquito breeding sites in Lucknow, India for potential mycopathogens of Anopheles stephensi.

During a short survey of soil and mosquito breeding sites in Lucknow, India for potential mycopathogen from a period of August-October 1996, 11 species of fungi in 5 genera were isolated using live mosquito larvae as host, Aspergillus flavus, A. fumigatus and Fusarium semitectum were the most frequently isolated species. Other fungi recorded were A. niger, A. ochraceus, A. terreus, A. versicolor, Geotrichum candidum, Penicillium verrucosum, Paecilomyces sp. and Fusarium sp. (Liseola/Elegans complex). Insect cell walls are known to contain chitin, so fungal isolates were tested for their chitinase activity on semi synthetic medium containing colloidal chitin. High chitinolytic activities were observed with A. flavus and A. ochraceus. Chitinase producers can be considered as potential pathogens. However, the higher incidence of F. semitectum could not be explained by inability to utilize chitin.

Animals↗

Application of 13C NMR to investigate the transformations and biodegradation of organic materials by wood- and soil-feeding termites, and a coprophagous litter-dwelling dipteran larva.

Solid-state 13C nuclear magnetic resonance spectroscopy has been used to characterize the C in samples of the food (wood), gut contents and faeces from the wood-feeding termite, Microcerotermes parvus; soil in the guts and mound material from the soil-feeding termite, Thoracotermes macrothorax; and the food and faeces from the litter-feeding, coprophagous larvae of the dipteran fly, Bibio marci. Spectra from the wood-feeding termite indicated preferential loss of polysaccharide and accumulation of lignin with some modification to the O-aromatic-C and methoxyl-C (O-methyl-C) components during passage through the gut. Spectra for the soil-feeding termite indicated little change in the distribution of 13C between resonances following passage through the gut, except for some evidence of preferential polysaccharide loss. Interpretation of the spectra from these organisms was restricted by the relatively low C content of the soils and mound material, and by the large contribution to the NMR spectra from the gut tissue rather than the gut contents. Spectra for the litter-feeding dipteran larvae indicated preferential feeding on the polysaccharide-rich component of the litter and then overall loss of polysaccharide-C and accumulation of both aromatic-C and methoxyl-C in the gut. These changes were greater for the second passage than for the first passage through the gut, suggesting that principally mechanical and physical changes occurred initially and that chemical digestion was prevalent during the second passage.

Animals↗

Nootkatone is a repellent for Formosan subterranean termite (Coptotermes formosanus).

We examined the behavior of Formosan subterranean termites toward one of the components of vetiver grass oil, the roots of which manufacture insect repellents. We found nootkatone, a sesquiterpene ketone, isolated from vetiver oil is a strong repellent and toxicant to Formosan subterranean termites. The lowest effective concentration tested was 10 micrograms/g substrate. This is the first report of nootkatone being a repellent to insects.

Animals↗

Correspondence of soldier defense secretion mixtures with cuticular hydrocarbon phenotypes for chemotaxonomy of the termite genus Reticulitermes in North America.

Soldier defense secretions from samples of Reticulitermes collected in California, Nevada, Arizona, New Mexico, and Georgia were characterized and correlated with cuticular hydrocarbon phenotypes. Twenty-seven cuticular hydrocarbon phenotypes have been defined, and soldier defense secretion (SDS) phenotypes have been described for 25 of these. Forty-five terpenoid compounds were found, including monoterpenes, sesquiterpenes, and a few diterpenes. The monoterpenes include (-)-alpha-pinene, (-)-beta-pinene, (-)-camphene, myrcene, (Z)- and (E)-ocimene, and (-)-limonene. The major sesquiterpenes produced are (+)-gamma-cadinene, (+)-gamma-cadinene aldehyde, (-)-germacrene A, germacrene B, gamma-himachalene, and beta-bisabolene. Some SDS phenotypes pair with more than one cuticular hydrocarbon phenotype; however, with two exceptions, each hydrocarbon phenotype is associated with only one SDS phenotype. These chemical characterizations lend support to the conclusion that there are numerous undescribed species of Reticulitermes in North America.

Adaptation, Physiological↗

Antitermitic activity of essential oils and components from Taiwania (Taiwania cryptomerioides).

Antitermitic activity of Taiwania (Taiwania cryptomerioides Hayata) against Coptotermes formosanus Shiraki was demonstrated in laboratory tests. Blocks of sapwood and heartwood from T. cryptomerioides exhibited antitermitic activity. Bioassays revealed that heartwood essential oil exhibited the highest antitermitic activity, followed by sapwood essential oil and then the n-C6H14 soluble fraction when tested at 10 mg/g. The order of termite mortality of three compounds purified from n-C6H14 soluble extracts of heartwood was cedrol > alpha-cadinol > ferruginol. The termite resistance of T. cryptomerioides wood can be attributed to the termiticidal activity of cedrol and alpha-cadinol.

Animals↗

Evaluation of vetiver oil and seven insect-active essential oils against the Formosan subterranean termite.

Repellency and toxicity of 8 essential oils (vetiver grass, cassia leaf, clove bud, cedarwood, Eucalyptus globules, Eucalyptus citrodora, lemongrass and geranium) were evaluated against the Formosan subterranean termite, Coptotermes formosanus Shiraki. Vetiver oil proved the most effective repellent because of its long-lasting activity. Clove bud was the most toxic, killing 100% of termites in 2 days at 50 micrograms/cm2. The tunneling response of termites to vetiver oil also was examined. Vetiver oil decreased termite tunneling activity at concentrations as low as 5 micrograms/g sand. Tunneling and paper consumption were not observed when vetiver oil concentrations were higher than 25 micrograms/g sand. Bioactivity of the 8 oils against termites and chemical volatility were inversely associated. Listed in decreasing order of volatility, the major constituents of the 8 oils were: eucalyptol, citronellal, citral, citronellol, cinnamaldehyde, eugenol, thujopsene, and both alpha- and beta-vetivone. Vetivor oil is a promising novel termiticide with reduced environmental impact for use against subterranean termites.

Animals↗

Extracts of Flourensia cernua (L): volatile constituents and antifungal, antialgal, and antitermite bioactivities.

The chemical components of tarbush (Flourensia cernua) leaves were fractionated by extracting successively with hexanes, diethyl ether, and ethanol. Volatile profiles of each fraction were identified by using GC-MS. The hexanes fraction contained mostly monoterpenoids, while the ethanol fraction volatiles were primarily sesquiterpenoids. Crude fractions were tested for activity against fungi, algae, and termites. Application of as little as 1 microg of the essential oil from the hexanes fraction was sufficient to provide visible antifungal activity in bioautography assays. The diethyl ether fraction showed selective activity against the cyanobacterium responsible for the 2-methylisoborneol-induced off-flavor sometimes associated with catfish farming operations. All three fractions exhibited a high degree of antitermite activity.

Animals↗

Hydroquinone: a general phagostimulating pheromone in termites.

The organization of termite societies depends predominantly on intraspecific chemical signals (pheromones) produced by exocrine glands, which induce and modulate individual behavioral responses. Here, the saliva-producing labial glands of termites were investigated with respect to their pheromonal role in communal food exploitation of termite colonies. From these glands, we identified for the first time hydroquinone (1,4-dihydroxybenzene) as a phagostimulating pheromone in the Australian termite species Mastotermes darwiniensis. Hydroquinone is released from the labial glands of termite workers and applied onto the food. It stimulates nestmates to feed at the spot of application and is, thus, employed to mark feeding sites. No synergistic effect with other identified labial gland compounds, such as glucose, inositol, and arbutin, was evident. Significantly, we show that termite species from all over the world, irrespective of taxonomic position and biological traits, produce and employ hydroquinone as phagostimulating signal. The use of the same chemical signal throughout an order is a unique phenomenon, not reported before in animals. Its possible biosynthetic pathway, ecological significance, and evolution are discussed.

Animals↗

Effects of plant flavonoids on fecundity, survival, and feeding of the Formosan subterranean termite.

Fecundity, mortality, and food consumption of the Formosan subterranean termite, Coptotermes formosanus Shiraki, were evaluated in response to five plant flavonoids (genistein, biochanin A, apigenin, quercetin, and glyceollin). Apigenin fed at 50 microg/primary reproductive pair proved to be the most toxic flavonoid. Biochanin A was most effective in reducing fecundity. Subsequently, these two flavonoids were tested through oral feeding and topical application at 100-microg dose. Significant reduction in the numbers of progeny was evident for biochanin A in both treatment methods. Choice feeding tests with termite workers showed that initially termites were attracted to filter paper treated with biochanin A, but over a period of 72 hr, consumed significantly less material when compared to controls. Biochanin A is a promising phytochemical with ability to reduce fecundity in primary reproductives of the Formosan subterranean termite, but it does not elicit phagostimulant activity.

Animals↗

Structure-activity of valencenoid derivatives and their repellence to the Formosan subterranean termite.

Eight valencenoid derivatives were evaluated for their repelling activity against Formosan subterranean termites, Coptotermes formosanus Shiraki. Among them, 1,10-dihydronootkatone was the strongest repellent, and valencene was the weakest. Results of the structure-repellency relationships indicated (1) reduction of the ketone group to the alcohol on position 2 of nootkatone curtailed the activity; (2) because of the low activity of valencene relative to nootkatone that the ketone group was essential for repellent activity; (3) reduction of the 1,10 double bond (1,10-dihydronootkatone and tetrahydronootkatone) produced compounds more repellent than nootkatone; (4) the isopropenyl group probably does not participate in binding as evidenced by no significant difference in the repellent activity among nootkatone (double bond between position 11 and 12), isonootkatone (double bond between position 7 and 11), and 11,12-dihydronootkatone.

Animals↗