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77 results for “terpenes”

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zenodo48/100

Dataset of report "A.2.2.6: Validation of the fitness of purpose of the performance assessment protocol developed in A2.1.4 by demonstrating its applicability for 2 terpenes using TD-GC/MS/FID and the static standards produced in A1.1.2."

<p>Dataset of report "A.2.2.6: Validation of the fitness of purpose of the performance assessment protocol developed in A2.1.4 by demonstrating its applicability for 2 terpenes using TD-GC/MS/FID and the static standards produced in A1.1.2."</p>

opencc-by-4.0Jul 2024View details →
zenodo44/100

Dataset: High emission rates and strong temperature response make boreal wetlands a large source of isoprene and terpenes

<p>Dataset used in the article &quot;High emission rates and strong temperature response make boreal wetlands a large source of isoprene and terpenes&quot;</p> <p>The tab-delimited file contains direct surface-atmosphere Volatile Organic Compound fluxes, measured by Eddy Covariance with a Vocus- proton transfer reaction mass spectrometer (Vocus-PTR) at a subarctic fen&nbsp;during 2021. It also contains PAR (Photosynthetic Active Radiation), temperature and flux&nbsp;quality criteria.</p>

opencc-by-4.0Aug 2022View details →
zenodo40/100

Transcriptomic analysis of deceptively pollinated Arum maculatum (Araceae) reveals association between terpene synthase expression in floral trap chamber and species-specific pollinator attraction

<p>A compressed folder containing the R script&nbsp;and input files required to replicate the results&nbsp;in our manuscript entitled &quot;Transcriptomic analysis of deceptively pollinated <em>Arum maculatum</em> (Araceae) reveals association between terpene synthase expression in floral trap chamber and species-specific pollinator attraction&quot;.</p> <p>Note: Raw Illumina sequencing files associated with this study have been uploaded to NCBI SRA, under the BioProject accession PRJNA856436.</p> <p><strong>ABSTRACT</strong></p> <p>Deceptive pollination often involves volatile organic compound (VOC) emissions that mislead insects into performing non-rewarding pollination. Among deceptively pollinated plants,&nbsp;<em>Arum maculatum</em>&nbsp;is particularly well-known for its potent dung-like VOC emissions and specialized floral chamber, which traps pollinators &ndash; mainly&nbsp;<em>Psychoda phalaenoides</em>and&nbsp;<em>P. grisescens</em>&nbsp;&ndash; overnight. However, little is known about the genes underlying the production of many&nbsp;<em>A. maculatum</em>VOCs, and their influence on variation in pollinator attraction rates. Therefore, we performed&nbsp;<em>de novo</em>&nbsp;transcriptome sequencing of&nbsp;<em>A. maculatum</em>&nbsp;appendix and male floret tissue collected during- and post-anthesis,&nbsp;from ten natural populations across Europe. These RNA-seq data were paired with&nbsp;GC-MS analyses&nbsp;of&nbsp;floral scent composition and pollinator data collected from the same inflorescences. Differential expression analyses revealed candidate transcripts in appendix tissue linked to malodourous VOCs including indole,&nbsp;<em>p</em>-cresol, and 2-heptanone. Additionally, we found that terpene synthase expression in male floret tissue during anthesis significantly covaried with sex- and species-specific attraction of&nbsp;<em>Psychoda phalaenoides</em>&nbsp;and&nbsp;<em>P.</em>&nbsp;<em>grisescens</em>. Taken together, our results provide the first insights into&nbsp;molecular mechanisms underlying pollinator attraction patterns in&nbsp;<em>A. maculatum</em>, and highlight&nbsp;floral chamber sesquiterpene (<em>e.g.</em>bicyclogermacrene)&nbsp;synthases as interesting candidate genes for further study.</p>

opencc-by-4.0Jul 2022View details →
zenodo40/100

Assessing the Cytotoxicity of Phenolic and Terpene Fractions Extracted from Iraqi Prunus arabica on AMJ-13 and SK-GT-4 Human Cancer Cell Lines

<p>Breast and esophagus cancer are the most aggressive and prominent causes of death worldwide. In addition, these cancers showed resistance to current chemotherapy regimens with limited success rates and fatal outcomes. Recently many studies reported the significant cytotoxic effects of phenolic and terpene fractions extracted from various <em>Prunus</em> species against different cancer cell lines. This suggests the probability to be a candidate as an alternative or adjuvant to the current chemotherapeutic regimens. The study aimed to evaluate the cytotoxicity of phenolic and terpene fractions extracted from Iraqi <em>Prunus arabica</em> on breast (AMJ-13) and esophagus (SK-GT-4) cancer cell lines by using the MTT assay. Analysis using Chou-Talalay method performed to assess the synergistic effect between the extracted fractions and chemotherapeutic agent (docetaxel). Moreover, HPLC analysis has been conducted for the quantitative determination of different bioactive molecule of both phenolic and terpene fractions in the extract. According to the findings, the treatment modalities significantly decreased cancer cell viability of AMJ-13 and SK-GT-4 and had insignificant cytotoxicity on the normal cells (normal human fibroblast cell line) (all less than 50% cytotoxicity). Analyzing with Chou-Talalay showed a strong synergism with docetaxel on both cancer cell lines (higher cytotoxicity even in low concentrations) and failed to induce a cytotoxicity on the normal cells. Important flavonoid glycosides and terpenoids were detected by HPLC in the particularly ferulic acid, catechin, chlorogenic acid, B sitosterol, and campesterol. In conclusion, the extracted fractions selectively inhibited the proliferation of both cancer cell and showed minimal cytotoxicity on normal cells. Thus, the study suggested the possible natural source of selected fractions as breast and esophagus cancer drugs</p>

opencc-by-4.0Feb 2023View details →
zenodo36/100

Polyketide-terpene hybrids from Pseudoxylaria

<p>This datasets contains data related to xylasporin derivatives. Extensive comparative spectrometric (HRMS<sup>2</sup>) and spectroscopic (1D and 2D NMR) studies allowed to determine the relative configuration across the xylasporin family, which was supported by chemical shift calculations of more than 50 stereoisomers and DP4+ probability analyses. The absolute configuration of xylasporin A (<strong>1</strong>) was also proposed based on TDDFT-ECD calculations. Additionally, we were able to revise the relative and absolute configurations of co-secreted xylacremolide B produced by single x-ray crystallography</p>

opencc-by-4.0Jun 2024View details →
zenodo36/100

Model data and code supporting "Updated Isoprene and Terpene Emission Factors for the Interactive BVOC Emission Scheme (iBVOC) in the United Kingdom Earth System Model (UKESM1.0) "

<p>Model data and analysis code supporting the Geoscientific Model Development manuscript &quot;Updated Isoprene and Terpene Emission Factors for the Interactive BVOC Emission Scheme (iBVOC) in the United Kingdom Earth System Model (UKESM1.0) &quot;</p> <p>&nbsp;</p> <p>&nbsp;</p>

opencc-by-4.0Mar 2023View details →
ClinicalTrials.gov36/100

Evaluation of an Oral Cannabidiol (CBD)-Terpene Formulation on Sleep Physiology in Participants With Insomnia

ClinicalTrials.gov study NCT05233761. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
dryad36/100

Water, not carbon, drives drought-constraints on stem terpene defense against simulated bark beetle attack in Pinus edulis

Open the record for dataset details and reuse information.

publicOct 2024View details →
zenodo32/100

Fig. 2 in Variation in the amino acids, volatile organic compounds and terpenes profiles in induced polyploids and in Solanum tuberosum varieties

Fig. 2. Biplot of Principal Component Analysis based on VOCs and Amino acids from leaves of Solanum allotetraploids (a), autotetraploids (b) and cultivated varieties (c). Components were calculated using Euclidean distances. Amino acids are depicted in the three-letter code. a) Allotetraploids (4xAL2 and 4xAL4) and diploid S. tuberosum x S. kurtzianum parental interspecific hybrid (2xPIH). b) Autotetraploids (4xAuL1, 4xAuL2 and 4xAuL3) and diploid S. kurtzianum parental line (2xPL). c) S. tuberosum cultivated varieties (4xCalen, 4xInnovator and 4xPampeana).

opennotspecifiedDec 2020View details →
zenodo32/100

Fig. 3 in Variation in the amino acids, volatile organic compounds and terpenes profiles in induced polyploids and in Solanum tuberosum varieties

Fig. 3. Hierarchical cluster analysis (represented by a heat-map) of amino acids content in leaves of potato allo- and autotetraploids and cultivated varieties. Dendrograms were constructed by UPGMA clustering method for 18 amino acids and 10 lines: diploid S. kurtzianum parental line (2xPL), diploid S. tuberosum x S. kurtzianum parental interspecific hybrid (2xPIH), three autotetraploids (4xAuL1, 4xAuL2 and 4xAuL3), two allotetraploids (4xAL2 and 4xAL4) and three cultivated varieties (4xCalen, 4xInnovator and 4xPampeana).

opennotspecifiedDec 2020View details →
zenodo32/100

Fig. 1 in Variation in the amino acids, volatile organic compounds and terpenes profiles in induced polyploids and in Solanum tuberosum varieties

Fig. 1. Fold change of compounds content in allotetraploids (a) and autotetraploids (b) relative to their respective diploid parental line. Fold change is expressed as log10(Tetraploid/Diploid). Horizontal lines are the average of the absolute logFC for each evaluated line, letters denote differences by Duncan's multiple range test (P &lt;0.05).

opennotspecifiedDec 2020View details →
zenodo32/100

Fig. 3 in Variation in the amino acids, volatile organic compounds and terpenes profiles in induced polyploids and in Solanum tuberosum varieties

Fig. 3. Hierarchical cluster analysis (represented by a heat-map) of amino acids content in leaves of potato allo- and autotetraploids and cultivated varieties. Dendrograms were constructed by UPGMA clustering method for 18 amino acids and 10 lines: diploid S. kurtzianum parental line (2xPL), diploid S. tuberosum x S. kurtzianum parental interspecific hybrid (2xPIH), three autotetraploids (4xAuL1, 4xAuL2 and 4xAuL3), two allotetraploids (4xAL2 and 4xAL4) and three cultivated varieties (4xCalen, 4xInnovator and 4xPampeana).

opennotspecifiedDec 2020View details →
zenodo32/100

Fig. 1 in Variation in the amino acids, volatile organic compounds and terpenes profiles in induced polyploids and in Solanum tuberosum varieties

Fig. 1. Fold change of compounds content in allotetraploids (a) and autotetraploids (b) relative to their respective diploid parental line. Fold change is expressed as log10(Tetraploid/Diploid). Horizontal lines are the average of the absolute logFC for each evaluated line, letters denote differences by Duncan's multiple range test (P &lt;0.05).

opennotspecifiedDec 2020View details →
zenodo32/100

Fig. 4 in Terpene chemotypes in Gossypium hirsutum (wild cotton) from the Yucatan Peninsula, Mexico

Fig. 4. Monoterpene composition of the two proposed cotton chemotypes. (a) Scatterplot of the relative abundance of the pinene group (α-Pinene + β-Pinene) against the relative abundance of the summed values of the γ-Terpinene group. (b) Representative chromatograms of plants belonging to chemotype classes A (upper panel) and B (lower panel). 1: (E)-2-Hexenal; 2: 2,4-Hexadienal (E,E); 3: α-Thujene; 4: α-Pinene; 5: Camphene; 6: Sabinene; 7: β-Pinene; 8: β-Myrcene; 9: α-Phellandrene; 10: α-Terpinene; 11: p-Cymene; 12: Limonene; 13: β-Phellandrene; 14: β-Ocimene; 15: γ-Terpinene; 16: Terpinolene; 17: Bornyl acetate; 18: γ-Elemene; 19: β-Caryophyllene; 20: α-Humulene; 21: Bicyclogermacrene. (c) visualisation of proportion of monoterpene compounds from panel (b), for each chemotype class.

opennotspecifiedJan 2023View details →
zenodo32/100

Fig. 1 in Terpene chemotypes in Gossypium hirsutum (wild cotton) from the Yucatan Peninsula, Mexico

Fig. 1. Map showing locations of the wild Gossypium hirsutum populations from which seeds were collected along the Yucatan Peninsula.

opennotspecifiedJan 2023View details →
zenodo32/100

Fig. 3 in Terpene chemotypes in Gossypium hirsutum (wild cotton) from the Yucatan Peninsula, Mexico

Fig. 3. Theorised monoterpenoid biosynthesis pathway. Compounds highlighted in blue comprise the γ-terpinene compound group, those highlighted in grey comprise the α-pinene compound group. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedJan 2023View details →
zenodo32/100

Fig. 5 in Terpene chemotypes in Gossypium hirsutum (wild cotton) from the Yucatan Peninsula, Mexico

Fig. 5. Principal coordinate analysis on relative abundance of monoterpenes in plants grown from seed, showing samples separated based on their compositional similarity.

opennotspecifiedJan 2023View details →
zenodo32/100

Fig. 6 in Terpene chemotypes in Gossypium hirsutum (wild cotton) from the Yucatan Peninsula, Mexico

Fig. 6. Ridgeline plot showing the distribution of the summed values of the γ-terpinene compound group (γ-terpinene, limonene, α-thujene, α-terpinene, terpinolene, and p-cymene; as % relative to total monoterpenes in each plant). In order from top to bottom: the plots coloured red (Celestún) and orange (Sisal) are located at the west of the peninsula. The plot coloured yellow (Chicxulub) is in the centre, and the cream coloured plot (Coloradas) is located at the east of the peninsula. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedJan 2023View details →
zenodo32/100

Fig. 2 in Terpene chemotypes in Gossypium hirsutum (wild cotton) from the Yucatan Peninsula, Mexico

Fig. 2. Correlation analysis of all mono- and sesquiterpenes analysed in the wild Gossypium hirsutum plants. Red rectangles indicate highly supported groups of monoterpenes (approximately unbiased (AU) p &lt;0.05). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedJan 2023View details →
zenodo32/100

Fig. 1 in Chemical diversity of k¯anuka: Inter- and intraspecific variation of foliage terpenes and flavanones of Kunzea (Myrtaceae) in Aotearoa/New Zealand

Fig. 1. Structures of key Kunzea compounds, showing reported 1H NMR chemical shifts of low field intramolecular hydrogen bonded OH in red (δ ppm). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedApr 2022View details →

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