Additional file 1: Table S1. of Global identification, structural analysis and expression characterization of bHLH transcription factors in wheat

Reference genes of bHLH genes expression analysis, the genes were downloaded from the database of NCBI. (XLSX 25 kb

Additional file 21: Figure S12. of Global identification, structural analysis and expression characterization of bHLH transcription factors in wheat

The wbHLH genes of block c showed higher expression levels in leaves at seedling stage. We obtained the result by blast tool that we used gene sequences mapped the 61 k wheat GeneChip in PLEXdb. The bHLH TFs of black c and gene probe were marked by the labels under each chart, respectively. (JPEG 2324 kb

Additional file 10: Table S7. of Global identification, structural analysis and expression characterization of bHLH transcription factors in wheat

Location of wheat bHLH on chromosome. (XLSX 16 kb

Additional file 22: Table S10. of Global identification, structural analysis and expression characterization of bHLH transcription factors in wheat

Correlation analysis of wbHLH genes expression pattern based on RNA-seq data and Q-PCR analysis. (XLSX 54 kb

Additional file 8: Figure S2. of Global identification, structural analysis and expression characterization of bHLH transcription factors in wheat

Multiple sequence alignment of the 225 wbHLH TF amino acid sequences. Shown at the top are the boundaries used in this study to distinguish the DNA-binding basic region, the two a-helixes and the variable loop region. (PDF 1236 kb

Aureochaeglobosins A–C, Three [4 + 2] Adducts of Chaetoglobosin and Aureonitol Derivatives from <i>Chaetomium globosum</i>

Aureochaeglobosins A–C (<b>1</b>–<b>3</b>), three novel [4 + 2] cycloaddition heterodimers of chaetoglobosin and aureonitol derivatives, were obtained from the culture of endophytic fungus <i>Chaetomium globosum</i>, representing the first adduct examples of chaetoglobosins. Their structures were elucidated by extensive spectroscopic analyses, single-crystal X-ray diffraction, and a modified Mosher’s method. Compounds <b>2</b> and <b>3</b> showed significant cytotoxicities against human MDA-MB-231 cancer cells with IC₅₀ values of 7.6 and 10.8 μM, respectively