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Phytochemistry

ISSN: 0031-9422

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Datasets associated with articles published in Phytochemistry

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1970
2024
1970 2024
1173 results
  • Data for: Polyploidy-induced variation in the amino acids, volatile organic compounds and terpenes profiles in potato
    Secondary metabolite content and amino acids content of diploid and tetraploid potato lines and varieties.
    • Dataset
  • Data for: Dimeric and esterified sesquiterpenes from the Liverwort Chiastocaulon caledonicum
    1D and 2D NMR spectra, UV-vis., IR, HREI-MS and polarimetry data of the new compounds : (+)-4α-acetoxy-gymnomitr-3(15)-ene (1), (+)-9α-acetoxy-gymnomitr-3(15)-ene (2), (-)-4-hydroxy-β-barbatene-9-cinnamate (3), (+)-1-oxo-gymnomitr-2β,15-diol (4), (+)-myltayl-5-one-4β-ol (8), chiastaucolin A (9) and chiastaucolin B (10) are shown in a single pdf file.
    • Dataset
  • Data for: Assessment of metabolic variability and diversity present in leaf, peel and pulp tissue of diploid and triploid Musa spp.
    The files contain data obtained from GCMS (single quadrupole), UPLC-PDA and LCMS (LC-QTof). The sample preparation with internal standard and sample analysis was performed as previously published for Musa tissue (Drapal et al., 2019). Samples were randomised and analysis performed in batches each including 20 samples, a quality control and an extraction blank. Aliquots for LC-ESI-QqTOF analysis (700 µl aqueous phase) were dried down and resuspended in methanol/water (100 µl, 1:1, v/v) under the addition of an internal standard. Homogentisic acid (5 µg/sample) was used for Fougamou and Mbi egome and genistein (2.5 µg/sample) for the diversity panel. Aliquots for UPLC-DAD analysis (700 µl organic phase) were dried down and resuspended in ethyl acetate/acetonitrile (1:9, v/v, leaf: 100 µl; peel and pulp: 50 µl). Aliquots for of peel and pulp sample extracts (140 µl aqueous phase) were dried down with an internal standard (d4-succinic acid, 10 µg/sample) and derivatised before analysis by GC-MS (EI, single quadrupole) in splitless mode with a temperature gradient of 70−325°C (Price et al., 2016). Data analysis and metabolite identification was also performed as previously reported for Musa tissue (Drapal et al., 2019). The resulting data tables comprised relative quantities (to the relevant internal standard) of metabolites detected by GC-MS and LC-MS and absolute quantities for metabolites measures by UPLC-DAD. All metabolites were expressed relative to the sample weight (µg/g dry wt.).
    • Dataset
  • Data for: Biotic and abiotic degradation of delta5-sterols in senescent Mediterranean marine and terrestrial angiosperms
    Efficiency of photooxidation processes in senescent leaves of marine and terrestrial angiosperms
    • Dataset
  • Data for: Recombinant production of labdane-type diterpenes in the green alga Chlamydomonas reinhardtii
    Alignment of CcCLS anbd CoCLS
    • Dataset
  • Data for: Heterocyst glycolipids indicate polyphyly of stigonematalean cyanobacteria
    The file contains relative abundances of heterocyst glycolipids in nostocalean and stigonematalean cyanobacteria.
    • Dataset
  • Data for: Metabolomic approach reveals the changes of metabolism in Isatis indigotica Fort. under nitrogen deficiency conditions
    The raw data of positive ion mode contained 4 quality control (QC) samples and 24 experimental samples, from which 1914 Peaks were extracted.
    • Dataset
  • Data for: Inoculation of Rhizoglomus irregulare or Trichoderma atroviride differentially modulates metabolite profiling of wheat root exudates
    raw dataset of metabolites profiled in root exudates of wheat following inoculation with either Rhizoglomus irregulare or Trichoderma atroviride
    • Dataset
  • Crinum x powellii transcriptome assembly and predicted peptide sequences
    Raw transcriptome assembly of Crinum x powellii (leaves, roots, bulbs, and in vitro cultures of calli grown in light (14h:10 light:dark cycles) or dark (24hs dark) and 2 mg/L or 4 mg/L of the synhetic auxin 2,4-dichlorophenoxyacetic acid) performed with the transcriptome assembler Trinity version 2.14.0, using default parameters. Plant growth protocol, RNA extraction and sequencing, quality control and annotation are described in the associated publication and raw reads were submitted to NCBI SRA under the BioProject PRJNA962562.
    • Dataset
  • Crinum x powellii transcriptome assembly and predicted peptide sequences
    Raw transcriptome assembly of Crinum x powellii (leaves, roots, bulbs, and in vitro cultures of calli grown in light (14h:10 light:dark cycles) or dark (24hs dark) and 2 mg/L or 4 mg/L of the synhetic auxin 2,4-dichlorophenoxyacetic acid) performed with the transcriptome assembler Trinity version 2.14.0, using default parameters. Plant growth protocol, RNA extraction and sequencing, quality control and annotation are described in the associated publication and raw reads were submitted to NCBI SRA under the BioProject PRJNA962562.
    • Dataset
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