2019
DOI: 10.1016/j.foodres.2018.12.036
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Comparison of triterpene compounds of four botanical parts from Poria cocos (Schw.) wolf using simultaneous qualitative and quantitative method and metabolomics approach

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Cited by 36 publications
(16 citation statements)
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“…The 1 H- and 13 C-NMR spectra indicated that H-11 (δ 5.37)/C-11 (δ 116.5), H-7 (δ 5.61)/C-7 (δ 121.0), C-9 (δ 146.4), C-8 (δ 142.7), H-18 (δ 1.01), H-19 (δ 1.07), H-26 (δ 1.67), H-27 (δ 1.62), H-28 (δ 1.22), H-29 (δ 1.13), H-30 (δ 1.06), H-3 (δ 3.46), H-24 (δ 5.33), C-3 (δ 77.9), C-21 (δ 178.9), C-24 (δ 124.8), C-25 (δ 131.5). Based on the structural features of triterpene compounds and the data given in the literature, compound- 4 was identified as dehydrotrametenolic acid [ 1 , 2 , 19 ]. Dehydrotrametenolic acid belongs to the lanosta-7,9(11)-diene type triterpenes [ 4 ].…”
Section: Resultsmentioning
confidence: 99%
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“…The 1 H- and 13 C-NMR spectra indicated that H-11 (δ 5.37)/C-11 (δ 116.5), H-7 (δ 5.61)/C-7 (δ 121.0), C-9 (δ 146.4), C-8 (δ 142.7), H-18 (δ 1.01), H-19 (δ 1.07), H-26 (δ 1.67), H-27 (δ 1.62), H-28 (δ 1.22), H-29 (δ 1.13), H-30 (δ 1.06), H-3 (δ 3.46), H-24 (δ 5.33), C-3 (δ 77.9), C-21 (δ 178.9), C-24 (δ 124.8), C-25 (δ 131.5). Based on the structural features of triterpene compounds and the data given in the literature, compound- 4 was identified as dehydrotrametenolic acid [ 1 , 2 , 19 ]. Dehydrotrametenolic acid belongs to the lanosta-7,9(11)-diene type triterpenes [ 4 ].…”
Section: Resultsmentioning
confidence: 99%
“…Additionally, P. cocos is used as a dietary supplement and in foods such as soups, dishes, snacks, and desserts for its health-promoting benefits. It can be divided into four parts, namely, Poriae Cutis (the epidermis, “fulingpi” in Chinese), Rubra Poria (the pink part near the epidermis), White Poria (the middle part, “baifuling” in Chinese), and Poria cum Radix Pini (the middle-plus-inner part, “fushen” in Chinese) [ 2 ]. Different parts of Poria cocos have different pharmacological effects and clinical applications.…”
Section: Introductionmentioning
confidence: 99%
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“…The data determined in this study not only lend sufficient support to the above literature but also determine the influence of the growth period on the triterpenoid acid content in four parts of Fushen. However, some studies have found that dehydropachymic acid and dehydrotumulosic acid contents are higher in the fulingpi (Zhang et al, 2019 ). This could be caused by different harvest times, according to the experimental results.…”
Section: Discussionmentioning
confidence: 99%
“…For triterpenoids, the cleavage at the glycosidic bonds was the fragmentation pattern and produced representative fragments with the loss of glucose (Glc, 162 Da), rhamnose (Rha, 146 Da), xylose (Xyl, 132 Da), and/or arabinose (Ara, 132 Da). However, these substances were prone to lose H Based on the cleavage rule of reference standards and information from related literature [2,[30][31][32][33][34][35][36], the triterpenoids could eliminate the neutral fragments such as Glc (162 Da), Rha (146 Da), Xyl (132 Da), Ara (132 Da), GlcA (176 Da), H 2 O (18 Da), CO2 (44 Da), HCOOH (46 Da), and/or the combination of these fragments. The characterization of triterpenoids in YWD was concluded by referring to these fragmentation mechanisms, and tentatively identified in YWD were a total of 59 triterpenoids, including 22 ginsenosides (labeled as P87, P89, P94-P96, P115, P122, P127-P128, P131, P136, P139, P145, P149-P151, P156, P182, P188, P192-P193, P208), 22 triterpene saponins (labeled as P181, P187, P203, P206, P209, P212-P213, P215, P217-P222, P224) and 15 triterpene acids (labeled as P103, P107-P110, P114, P116, P119, P135, P137, P140-P141, P146-P147, P152, P157-P158, P163, P170, P172, P180, P184) (Table S3).…”
Section: Characterization Of Triterpenoids In Ywdmentioning
confidence: 99%