| 1. |
- El-Seedi, Hesham, et al.
(författare)
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Biosynthesis, natural sources, dietary intake, pharmacokinetic properties, and biological activities of hydroxycinnamic acids
- 2012
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Ingår i: Journal of Agricultural and Food Chemistry. - : American Chemical Society (ACS). - 0021-8561 .- 1520-5118. ; 60:44, s. 10877-10895
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Forskningsöversikt (refereegranskat)abstract
- Hydroxycinnamic acids are the most widely distributed phenolic acids in plants. Broadly speaking, they can be defined as compounds derived from cinnamic acid. They are present at high concentrations in many food products, including fruits, vegetables, tea, cocoa, and wine. A diet rich in hydroxycinnamic acids is thought to be associated with beneficial health effects such as a reduced risk of cardiovascular disease. The impact of hydroxycinnamic acids on health depends on their intake and pharmacokinetic properties. This review discusses their chemistry, biosynthesis, natural sources, dietary intake, and pharmacokinetic properties.
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| 2. |
- Eiras, A. E., et al.
(författare)
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Sex pheromone of the Brazilian apple leafroller, Bonagota cranaodes Meyrick (Lepidoptera, Tortricidae)
- 1999
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Ingår i: Zeitschrift für Naturforschung C - A Journal of Biosciences. - : Walter de Gruyter. - 0939-5075 .- 1865-7125. ; 54:7-8, s. 595-601
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Tidskriftsartikel (refereegranskat)abstract
- The female sex pheromone of Bonagota (=Phthteochroa) cranaodes (Meyrick) is a blend of (E,Z)-3,5-dodecadienyl acetate (E3,Z5-12:Ac) and (Z)-9-hexadecenyl acetate (Z9-16:Ac) according to analysis of pheromone - gland extracts and field trapping in apple orchards. This is the first time that E3,Z5-12:Ac has been identified as a lepidopteran sex pheromone. Traps baited with 100 mu g E3,Z5-12:Ac were attractive over 15 weeks in the field and were as effective as traps baited with virgin females. Addition of Z9-16:Ac to E3,Z5-12:Ac at ratio of 1:10 had a significantly increase of male moths. The addition of the Z,E and Z:Z isomers to rubber septa baited with E3,Z5-12:Ac did not modify B. cranaodes male attraction, but 10% of EE enhanced trap catch.
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| 3. |
- Borg Karlson, A. K., et al.
(författare)
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Floral fragrance chemistry in the early flowering shrub Daphne mezereum
- 1996
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Ingår i: Phytochemistry. - : Elsevier BV. - 0031-9422 .- 1873-3700. ; 41:6, s. 1477-1483
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Tidskriftsartikel (refereegranskat)abstract
- The floral fragrance of the shrub Daphne mezereum in central Sweden was collected by means of the head-space technique and investigated by GC-MS and multi-dimensional GC. (S)-(+)-Linalool was the main constituent (95%) of the flower fragrance and its enantiomeric purity exceeded 99% in the samples. The (2S, 5S)- and (2R, 5S)-furanoid and the (3R, 6S)- and (3S, 6S)-pyranoid linalool oxide isomers constituted 2-5% of the fragrance. The elution order of these compounds on a permethylated beta-cyclodextrin column is reported. A fragrance sample of D. mezereum as well as (S)-(+)-linalool attracted males of the vernal solitary bee species Colletes cunicalarius and Andrena cinerea. A racemic mixture of the two enantiomeric pairs of known furanoid linalool oxides was only weakly attractive to the bees. The role of the fragrance in the pollination specialization of the plant is discussed.
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| 4. |
- Karlson, J., et al.
(författare)
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Inhibition of tumor cell growth by monoterpenes in vitro : Evidence of a Ras-independent mechanism of action
- 1996
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Ingår i: Anti-Cancer Drugs. - : Ovid Technologies (Wolters Kluwer Health). - 0959-4973 .- 1473-5741. ; 7:4, s. 422-429
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Tidskriftsartikel (refereegranskat)abstract
- (+)-Limonene (d-limonene) and related monoterpenes show chemopreventive activity against rodent mammary carcinoma and inhibit the growth of cancer cells in vitro, One suggested mechanism for the anti-tumorigenic effect of (+)-limonene is inhibition of the post-translational isoprenylation of growth controlling Pas oncoproteins. We have here examined the growth inhibitory effects of (+)-limonene and other related monoterpenes on PANC-1 pancreas carcinoma cells (carrying a K-ras mutation) and on 12V-H-ras-transformed rat fibroblasts, (+)- and (-)-perillyl alcohol, 7-methyl-perillyl alcohol, (+)-limonene oxide and (+)-perillic acid methyl ester were all found to efficiently inhibit cell growth at 1 mM, whereas (+)-limonene caused an approximately 50% growth reduction at 5 mM, Whereas BZA-BB, an inhibitor of Ras farnesyl transferase, was found to induce morphological reversion of 12v-H-ras-transformed cells, (+)-perillyl alcohol and (+)-limonene did not induce reversion. Furthermore, monoterpenes did not decrease MAP kinase enzyme activity or collagenase promoter activity in PANC-1 cells, two functions known to be down-stream from Pas, We conclude that although effective in inhibiting the growth of tumor cells harboring activated res oncogenes, limonene and (+)-perillyl alcohol are unlikely to act by inhibiting Ras function.
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| 7. |
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| 9. |
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| 10. |
- Luxova, A., et al.
(författare)
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Absolute configuration of chiral terpenes in marking pheromones of bumblebees and cuckoo bumblebees
- 2004
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Ingår i: Chirality. - : Wiley. - 0899-0042 .- 1520-636X. ; 16:4, s. 228-233
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Tidskriftsartikel (refereegranskat)abstract
- The absolute configurations of citronellol, 2,3-dihydrofamesol, and 2,3-dihydrofarnesal in male marking pheromones of seven species of bumblebees and cuckoo bumblebees were determined by enantioselective gas chromatography on a capillary column coated with 60% heptakis(2,3-di-O-acetyl-6-O-TBDMS)-beta-cyclodextrin in polysiloxane PS 268. Pure (-)-S-enantiomers of all three terpenes were found in the labial glands of all investigated specimens of the following species: Bombus (Bombus) terrestris, B. (Bombus) lucorum, B. (Pyrobombus) pratorum, B. (Pyrobombus) pyrenaeus, B. (Pyrobombus) jonellus, B. (Pyrobombus) impatiens, and the cuckoo bumblebee B. (Ashtonipsithyrus) bohemicus. Within species, specimens were collected at different localities and in different years. Except for 2,3-dihydrofamesol in B. terrestris, this is the first report on the absolute configuration of terpenes in marking pheromones of bumblebees.
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| 11. |
- Mozuraitis, Raimondas, et al.
(författare)
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Chemocommunication in Phyllonorycter ulmifoliella (HBN.) (Lepidoptera: Gracillariidae) : Periodicity, Sex Pheromone, and Inhibitors
- 1997
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Ingår i: Journal of Chemical Ecology. - 0098-0331 .- 1573-1561. ; 23:1, s. 175-189
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Tidskriftsartikel (refereegranskat)abstract
- (Z)-10-Tetradecenyl acetate (Z10-14:OAc) from abdominal tip extracts of virgin females of the tentiform leafminer moth Phyllonorycter ulmifoliella (Lepidoptera: Gracillariidae) was identified by gas chromatography and mass spectrometry. The biological activity of the component was confirmed by field tests with synthetic compounds. As a sex pheromone component this ester is novel both in the family Gracillariidae and in the superfamily Gracillarioidea. Field trapping of P. ulmifoliella with synthetic Z10-14:OAc at dosages of 1 and 0.2 mg/dispenser led to catches of approximately 9000 and 3000 male moths, respectively. The attractivity of the Z10-14:OAc was strongly inhibited by a 10% admixture of either (Z)-9-tetradecenyl acetate (Z9-14:OAc), (E)-9-tetradecenyl acetate (E9-14:OAc), or (E)-11-tetradecenyl acetate (E11-14:OAc). Addition of 10% (E)-10-tetradecenyl acetate (E10-14:OAc) to the sex pheromone reduced attractivity, but significantly less than the inhibitors previously mentioned. The pheromone releasing (or ‘’calling”) behavior of virgin P. ulmifoliella females was recorded under laboratory conditions. Calling activity started about half an hour before lights-on and the maximum number of calling females was registered half an hour after the start of photophase. A high level of pheromone releasing activity lasted for about 2 hr and ceased about 5 hr after the start of photophase. Chemocommunication activity in the light period of day is assumed to be an adaptation which allows this phyllonoryctid to avoid inhibitors emitted as pheromones by many other species. A scheme of probable interactions by means of semiochemicals between P. ulmifoliella and other lepidopterans is presented and the appearance of Z10-14:OAc as a sex pheromone component in Lepidoptera during evolution of the order is discussed.
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| 12. |
- Mozuraitis, Raimondas, et al.
(författare)
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New sex attractants and inhibitors for 17 moth species from the families Gracillariidae, Tortricidae, Yponomeutidae, Oecophoridae, Pyralidae and Gelechiidae
- 1998
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Ingår i: Journal of applied entomology. - : Wiley. - 0931-2048 .- 1439-0418. ; 122:8, s. 441-452
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Tidskriftsartikel (refereegranskat)abstract
- Field screening tests of 21 saturated and monounsaturated straight chain C-12 and C-14 alcohols and their acetates as well as some binary mixtures in dosages of 1 and 0.2 mg/dispenser were carried out in Lithuanian in 1993 and 1994. New sex attractants were determined for males of five moth species of the family Gracillariidae (E10-12:OH for Phyllonorycter soi bi, E10-12Ac for Ph. cydoniella and Ph. oxyacanthae, Z10-12:OAc for Ph. junoniella, and a mixture of Z10-14:OAc with E9-14:OAc in a 1:10 for Pit. sylvella), for four species of the family Tortricidae (E10-14:OAc for Endothenia ericetana, Z10-14:OAc in a 10:1 mixture with E11-14:OAc for Eudemis pozphyrana, E11-14:OAc in a 10:1 mixture with E11-14:OH for Dichrorampha petiverella and Cochylis dubitana), for two species of Gelechiidae (Z9-14:OAc in a mixture with either Z10-14:OAc in a ratio 1:1, E9-14:OAc in a ratio 1:10 or E10-14:OAc in a ratio 10:1 for Bryotropha galbanella, Z10-14:OAc and E9-14:OAc in a ratio 10:1 for B. mundella), as well as for one species of each of the families Yponomeutidae (Z7-14:OAc for Paraswammerdamia lutarea) and Oecophoridae (Z10-14:OAc and E9-14:OAc in a ratio 10:1 for Pseudatemelia josephinae). Preliminary composition of sex attractants was established for three moth species of the family Gracillariidae (Z10-14:OAc in a 1.10 mixture with E9-14:OAc for Phyllonorycter heegerella, Ph. coryli and Ph. dubitella) and for one species of the family Gelechiidae (Z9-14:OAc for Bryotropha terella). Inhibitors of the sex attractants were found for four leafminer species of the family Gracillariidae (Z7-, Z9- and Z10-12:OAc for Phyllonorycter sorbi, Z10-, E10-12:OH and E10-14:OH for Ph. mespilella, E10-12:OH for Ph. cydoniella, Z10-12:OH and E10-14:OH for Ph. oxyacanthae), for three species of Tortricidae (E9-, Z11- and E11-14:OAc for Endothenia ericetana, E11-14:OAc for Gypsonoma minutana, E10- and E11-14:OAc for Epagoge grotiana), and for one species from the family Pyralidae (Z10-, E10- and E11-14:OAc for Pyrausta aurata). Data from male behaviour tests in tube olfactometers are presented for Phyllonorycter blancardella, Ph. sorbi, Ph. dubitella and Ph. strigulatella and active compounds revealed.
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| 13. |
- Mozuraitis, Raimondas, et al.
(författare)
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Sex pheromone of the spotted tentiform leafminer moth Phyllonorycter blancardella (Fabr.) (Lep., Gracillariidae)
- 1999
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Ingår i: Journal of applied entomology. - : Wiley. - 0931-2048 .- 1439-0418. ; 123:10, s. 603-606
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Tidskriftsartikel (refereegranskat)abstract
- Dodecyl acetate (12:OAc) (E)-10-dodecenyl acetate (E10-12:OAc) and (E)-10-dodecenol (E10-12:OH) in the ratio 8:80:12 were collected by solid phase micro-extraction of the volatiles emitted by virgin signalling females of the spotted tentiform leafminer moth, Phyllonorycter blancardella. The same compounds in the ratio 8:79:13 were extracted from the sex pheromone glands of virgin signalling females of the same species. The chemical structures of the compounds were identified by gas chromatography and mass spectrometry. Trapping results obtained from field tests using synthetic components of the sex pheromone demonstrated that only one component, E10-12:OAc, was essential for the attraction of conspecific males and should be considered as a sex pheromone.
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| 14. |
- Pettersson, Marie, et al.
(författare)
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Semiochemicals related to the aphid Cinara pilicornis and its host, Picea abies: A method to assign nepetalactone diastereomers
- 2008
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Ingår i: Journal of Chromatography A. - : Elsevier. - 0021-9673 .- 1873-3778. ; 1180:1-2, s. 165-170
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Tidskriftsartikel (refereegranskat)abstract
- Volatiles released by seedlings of Norway spruce infested with the aphid Cinara pilicornis were analyzed using SPME–GC–MS. Among the stress-induced compounds released by the host plant, citronellol, cis–trans-nepetalactone and cis–trans-nepetalactol was found. These compounds originated from the aphids and they were assumed to be pheromone components for this aphid species. To determine the relative stereochemistry of the nepetalactone, a diagnostic method was developed. The method was based on multivariate analysis of tabulated relative intensities of mass fragments of the four nepetalactone diastereomers. In the practical method described, a few pairs of fragments in the mass spectra were compared and, in combination with the Kovat's index, were used to unambiguously identify the relative stereochemistry of the nepetalactone.
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| 15. |
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