AI Article Synopsis

  • A phytochemical study on the methanol extract of stems and leaves led to the discovery of six dibenzocyclooctadiene lignans, including three new compounds named kadsindutalignans A, B, and C.
  • Their structures were identified through various spectroscopic techniques like HRESIMS and NMR, which provided detailed insights into their molecular configurations.
  • All isolated compounds demonstrated the ability to inhibit NO production in LPS-activated RAW264.7 cells, with the new compound showing particularly strong activity, surpassing the effectiveness of the positive control (L-NMMA).

Article Abstract

Phytochemical study on the methanol extract of the stems and leaves of led to the isolation of six dibenzocyclooctadiene lignans, including three new compounds named kadsindutalignans A-C (), and three known ones, heteroclitalignan B (), kadsuphilin C () and kadsulignan E (). Their structures were elucidated based on extensive spectroscopic analyses, including HRESIMS, 1D- (H NMR and C NMR), 2D-NMR (HSQC, HMBC, H-H COSY and NOESY), and experimental circular dichroism (CD) spectra. All the isolates inhibited NO production in LPS-activated RAW264.7 cells with IC values in the range from 5.67 ± 0.54 µM to 38.19 ± 2.03 µM, compared to that of the positive control of -monomethyl-L-arginine acetate (L-NMMA) with an IC value of 8.90 ± 0.48 µM. Interestingly, the new compound showed potential inhibition of NO production with an IC value of 5.67 ± 0.54 µM, which was higher than that of the positive control.

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http://dx.doi.org/10.1080/14786419.2022.2134361DOI Listing

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Article Synopsis
  • A phytochemical study on the methanol extract of stems and leaves led to the discovery of six dibenzocyclooctadiene lignans, including three new compounds named kadsindutalignans A, B, and C.
  • Their structures were identified through various spectroscopic techniques like HRESIMS and NMR, which provided detailed insights into their molecular configurations.
  • All isolated compounds demonstrated the ability to inhibit NO production in LPS-activated RAW264.7 cells, with the new compound showing particularly strong activity, surpassing the effectiveness of the positive control (L-NMMA).
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