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eclipse 400 nmr spectrometer  (JEOL)


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    JEOL eclipse 400 nmr spectrometer
    Eclipse 400 Nmr Spectrometer, supplied by JEOL, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/eclipse 400 nmr spectrometer/product/JEOL
    Average 90 stars, based on 1 article reviews
    eclipse 400 nmr spectrometer - by Bioz Stars, 2026-05
    90/100 stars

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    Chemical structures of compounds isolated from the endophytic fungus Alternaria alternata . Ergosterol (1), β -Sitosterol (2), Ergosterol peroxide (3), Fonsecinone A (4), Asperpyrone C (5), and Asperpyrone B (6), showing observed key <t>HMBC</t> correlations of compounds 4, 5 and 6
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    Chemical structures of compounds isolated from the endophytic fungus Alternaria alternata . Ergosterol (1), β -Sitosterol (2), Ergosterol peroxide (3), Fonsecinone A (4), Asperpyrone C (5), and Asperpyrone B (6), showing observed key HMBC correlations of compounds 4, 5 and 6

    Journal: AMB Express

    Article Title: Antimicrobial, antiproliferative activities and molecular docking of metabolites from Alternaria alternata

    doi: 10.1186/s13568-023-01568-1

    Figure Lengend Snippet: Chemical structures of compounds isolated from the endophytic fungus Alternaria alternata . Ergosterol (1), β -Sitosterol (2), Ergosterol peroxide (3), Fonsecinone A (4), Asperpyrone C (5), and Asperpyrone B (6), showing observed key HMBC correlations of compounds 4, 5 and 6

    Article Snippet: 1D ( 1 H and 13 C) NMR and 2D (HMQC and HMBC) NMR spectra were recorded on a JEOL Eclipses ECS-400 NMR spectrometer (JEOL in., Peabody, MA, USA) at 400 MHz for 1 H NMR and 100 MHz for 13 C NMR, using the residual solvent peak ( H = 7.26 and C = 77.1, CDCl 3 ) as a reference.

    Techniques: Isolation

    1 H and 13 C-NMR, and HMBC spectral data and HMBC correlations of compounds 4, 5 and 6 (CDCl 3 , δ in ppm, J in Hz)

    Journal: AMB Express

    Article Title: Antimicrobial, antiproliferative activities and molecular docking of metabolites from Alternaria alternata

    doi: 10.1186/s13568-023-01568-1

    Figure Lengend Snippet: 1 H and 13 C-NMR, and HMBC spectral data and HMBC correlations of compounds 4, 5 and 6 (CDCl 3 , δ in ppm, J in Hz)

    Article Snippet: 1D ( 1 H and 13 C) NMR and 2D (HMQC and HMBC) NMR spectra were recorded on a JEOL Eclipses ECS-400 NMR spectrometer (JEOL in., Peabody, MA, USA) at 400 MHz for 1 H NMR and 100 MHz for 13 C NMR, using the residual solvent peak ( H = 7.26 and C = 77.1, CDCl 3 ) as a reference.

    Techniques: