2020
DOI: 10.1007/s10600-020-02979-3
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Steroidal Compounds from Roots of Cinnamomum camphora

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Cited by 2 publications
(2 citation statements)
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“…Compound 5 was also compared with the known compounds 7 β -hydroperoxycholesterol and 7 α -hydroperoxycholesterol in order to define the stereo center C-7 [ 19 ]. In terms of the chiral center C-24 on the side chain, the 1D NMR data were compared with those of (24 R )-campesterol and (24 S )-methylcholesterol [ 23 , 24 ]. Based on the previous literature and NOE correlations, the absolute configuration of 5 was proposed to be 3 S , 7 R , and 24 S .…”
Section: Resultsmentioning
confidence: 99%
“…Compound 5 was also compared with the known compounds 7 β -hydroperoxycholesterol and 7 α -hydroperoxycholesterol in order to define the stereo center C-7 [ 19 ]. In terms of the chiral center C-24 on the side chain, the 1D NMR data were compared with those of (24 R )-campesterol and (24 S )-methylcholesterol [ 23 , 24 ]. Based on the previous literature and NOE correlations, the absolute configuration of 5 was proposed to be 3 S , 7 R , and 24 S .…”
Section: Resultsmentioning
confidence: 99%
“…Apart from analgesic, Kafūr has also been reported for many other pharmacological activities might be due to the presence of monoterpenes, phenolic derivatives, flavonoids, lignans, sterols, and terpenoids [34,37,39,40,[43][44][45]46]; which are reported to have antinociceptive/analgesic [49,50], antioxidant [52], antimicrobial [53][54][55][56][57] and wound healing properties [64]. The antibacterial activity was achieved by different mechanisms like partial degradation of the cell membrane, increased membrane permeability, cytoplasm leakage, noticeable distortion, shrinkage of bacterial cells, and membrane protein structural changes [56].…”
Section: Discussionmentioning
confidence: 99%