1998
DOI: 10.1016/s0031-9422(97)00994-1
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Monoterpene alkaloids, iridoids and phenylpropanoid glycosides from Osmanthus austrocaledonica

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Cited by 33 publications
(13 citation statements)
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“…S18, S20). These could be GL5, previously been reported from F. excelsior 27,35 , or isomers jaspolyanoside, austrosomide and/or 6′-elenolylnicotiflorine 41,48,49 . The m/z 259/291 fragment ion pair is also observed in the MS2 spectra of the nuzhenide isomers 2, 18 and 20, and are absent from their isomer 3.…”
Section: Confirmation Of 1-4 As Secoiridoid Glycosides and Identificamentioning
confidence: 59%
“…S18, S20). These could be GL5, previously been reported from F. excelsior 27,35 , or isomers jaspolyanoside, austrosomide and/or 6′-elenolylnicotiflorine 41,48,49 . The m/z 259/291 fragment ion pair is also observed in the MS2 spectra of the nuzhenide isomers 2, 18 and 20, and are absent from their isomer 3.…”
Section: Confirmation Of 1-4 As Secoiridoid Glycosides and Identificamentioning
confidence: 59%
“…A minor iridoid named austromoside 219 was found in Osmanthus austrocaledonica (216), and fraxiformoside 220 was isolated from Fraxinus formosana (217) and Fraxinus malacophylla (218). Framoside 221, which has anti-inflammatory activity, was isolated from Fraxinus species (219); neooleuropein 222 was isolated from Fraxinus chinensis (220); and fraximalacoside 223 was isolated from F. malacophylla (218).…”
Section: Phenylethanoid Glycosidesmentioning
confidence: 99%
“…Up to now, there has been no detailed research on the extraction procedures for these chemical constituents. Generally, the crude extracts wer prepared with different concentrations of methanol, ethanol or acetone-water solution by the impregnation method, refluxing extraction or decoction method [10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,…”
Section: Chemical Constituentsmentioning
confidence: 99%