2022
DOI: 10.1016/j.phytochem.2022.113241
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Identification and structural elucidation of bioactive compounds from Scirpoides holoschoenus

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Cited by 3 publications
(3 citation statements)
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“…Moreover, the HPLC-UV chromatogram of the PRC fraction was almost identical to that of the DEE fraction of the methanolic extract of the rhizomes and roots of Scirpoides holoschoenus L., except for the lipophilic region at the end (Figure S5). In comparison to the published data [47], the HPLC-DAD and HPLC-ESI-MS analysis indicated the presence of two stilbene dimers: scirpusin A (21) and cassigarol E (26), five stilbene trimers: cyperusphenol D (20), passiflorinol A (22), cyperusphenol A (24), mesocyperusphenol A (25), and passiflorinol B (23), and one ferulic acid derivative: smiglaside C (27) in the PRC fraction of the methanolic extract of C. articulatus, in addition to 2R/2S dihydroluteolin (14), piceatannol (16), trans-scirpusin B (17), and cyperusphenol B (19), which were already isolated and tested. Finally, the PRC fraction, containing many potentially active stilbene oligomers, might be interesting for further investigations as well.…”
Section: Discussionmentioning
confidence: 84%
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“…Moreover, the HPLC-UV chromatogram of the PRC fraction was almost identical to that of the DEE fraction of the methanolic extract of the rhizomes and roots of Scirpoides holoschoenus L., except for the lipophilic region at the end (Figure S5). In comparison to the published data [47], the HPLC-DAD and HPLC-ESI-MS analysis indicated the presence of two stilbene dimers: scirpusin A (21) and cassigarol E (26), five stilbene trimers: cyperusphenol D (20), passiflorinol A (22), cyperusphenol A (24), mesocyperusphenol A (25), and passiflorinol B (23), and one ferulic acid derivative: smiglaside C (27) in the PRC fraction of the methanolic extract of C. articulatus, in addition to 2R/2S dihydroluteolin (14), piceatannol (16), trans-scirpusin B (17), and cyperusphenol B (19), which were already isolated and tested. Finally, the PRC fraction, containing many potentially active stilbene oligomers, might be interesting for further investigations as well.…”
Section: Discussionmentioning
confidence: 84%
“…HPLC-UV chromatogram (205 nm) and peak assignment of the (A) PE fraction and (B) DEE fraction of the methanolic rhizomes and roots extract of Cyperus articulatus; for HPLC conditions, see Section 4.2 (General experimental methods). Due to a similar extract composition, the HPLC method for the DEE fraction of the methanolic rhizomes and roots extract, after DCM extraction of Scirpoides holoschoenus, was used for the DEE fraction of C. articulatus in (B)[47].…”
mentioning
confidence: 99%
“…For the structural identification of crude extracts, the NMR spectra of the crude extracts were compared with the NMR spectra of compounds already identified in the database to determine the structures of the compounds [236]. For unknown compounds, the structure of natural products can be analyzed by one-and two-dimensional NMR spectroscopy combined with mass spectrometry [237][238][239].…”
Section: Nuclear Magnetic Resonance Spectroscopy (Nmr)mentioning
confidence: 99%