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14 results for “Eutypella”
FIG. 13. — Eutypella naqsii K.D in Modern taxonomic approaches to identifying diatrypaceous fungi from marine habitats, with a novel genus Halocryptovalsa Dayarathne & K.D.Hyde, gen. nov.
FIG. 13. — Eutypella naqsii K.D.Hyde (BRIP 22588, holotype). A, herbarium material; B, horizontal section through ascostroma; C, D, vertical section through ascoma; E, peridium; F, paraphyses; G-I, asci; J-N, ascospores. Scale bars: B, 1000 μm; C, 500 μm; D,100 μm; E, F-I, 20 μm; J, 10 μm; K-N, 5 μm.
Fig. 9 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 9. Experimental ECD spectrum of 7c in MeOH. The arrow indicated the electric transition dipole of the chromophores.
Fig. 10 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 10. ECD spectra of the Mo2(AcO)4 complex of 9 (A) and 16 (B) in DMSO.
Fig. 7 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 7. ΔδH (δRS = δR ‒ δS) values of MPA esters of 3, 4, 7, 8, and 10.
Fig. 4 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 4. Experimental ECD spectra of 1‒5 and 18 in MeOH.
Fig. 3 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 3. Key NOE correlations of 1, 6, and 13–15.
Fig. 6 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 6. Production of 2a and 2b and the ΔδH (δR ‒ δS) values of 2c and 2d.
Fig. 2 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 2. Key COSY and HMBC correlations of 1, 6, and 13–15.
Fig. 8 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 8. Experimental and calculated ECD spectra of 6, 11, 12, and 15 in MeOH.
Fig. 1 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 1. Structures of sesquiterpenes 1–21.
Fig. 13 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 13. Putative biogenetic relationships of the sesquiterpenes.
Fig. 12 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 12. Key NOE correlations of 16 and 17.
Fig. 11 in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 11. Linear regression analysis of the experimental and calculated 13C NMR chemical shifts for 10 12. Correlation plots of the experimental 13C NMR data of 10 – and calculated values of (1S*,2R*,6R*,7S*)-10 (10a, A) and (1S*,2R*,6R*,7R*)-10 (10b, B). Correlation plots of the experimental 13C NMR data of 11 and calculated values of (1S*,6R*,7S*)-11 (11a, C) and (1S*,6R*,7R*)-11 (11b, D). Correlation plots of the experimental 13C NMR data of 12 and calculated values of (1S*,6R*,7R*)-12 (12a, E) and (1S*,6R*,7S*)-12 (12b, F).
Fig. 5. X in Chemical epigenetic manipulation triggers the production of sesquiterpenes from the deep-sea derived Eutypella fungus
Fig. 5. X-ray crystallographic structure of 1.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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International Brain Laboratory public data
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OpenNeuro
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