2021
DOI: 10.1007/s11418-021-01581-3
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Constituents of Morus alba var. multicaulis leaf improve lipid metabolism by activating the AMPK signaling pathway in HepG2 cells

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Cited by 6 publications
(7 citation statements)
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“…It had a molecular formula of C 19 H 30 O 10 as determined by positive HRESIMS with a [M + Na] + ion peak at m/z 441.1734 (calcd for C 19 H 30 O 10 Na + , 441.1731). The 1 H and 13 C NMR data (Table 1) of 1 were similar to those of 2-[4-(3-hydroxypropyl)-2methoxyphenoxy]propane-1,3-diol [10] except for a hexose residue in 1. In addition, the chemical shift of C-9 of 1 was shifted downfield by 4.1 ppm, indicating the sugar group was located at C-9 position.…”
Section: Resultsmentioning
confidence: 77%
See 1 more Smart Citation
“…It had a molecular formula of C 19 H 30 O 10 as determined by positive HRESIMS with a [M + Na] + ion peak at m/z 441.1734 (calcd for C 19 H 30 O 10 Na + , 441.1731). The 1 H and 13 C NMR data (Table 1) of 1 were similar to those of 2-[4-(3-hydroxypropyl)-2methoxyphenoxy]propane-1,3-diol [10] except for a hexose residue in 1. In addition, the chemical shift of C-9 of 1 was shifted downfield by 4.1 ppm, indicating the sugar group was located at C-9 position.…”
Section: Resultsmentioning
confidence: 77%
“…The eight known analogues were identified as eugenyl-α-larabinofuranosyl-(1!6)-β-d-glucopyranoside (5), [13] canthoside A (6), [14] icariside D 1 (7), [15] 3-hydroxyphenethyl alcohol 4-O-β-dglucopyranoside (8), [16] henryoside (9), [17] virgaureoside A (10), [18] (+)-syringaresinol 4-O-β-d-glucoside (11), [19] and (7R,8S)-erythro-7,9,9'-trihydroxy-3,3'-dimethoxy-8-O-4'-neolignan-4-O-β-d glucopyranoside (12) [20] glucopyranoside (12) [20] by comparison of the spectroscopic results and literature data.…”
Section: Resultsmentioning
confidence: 99%
“…Twenty-two known compounds were identified as quercetin-3- O - β -D-rhamnopyranoside ( 4 ) [ 17 ], 6-methoxy-naringenin ( 5 ) [ 18 ], 6-methoxy-kaempferol ( 6 ) [ 19 ], kaempferol ( 7 ) [ 20 ], apigenin ( 8 ) [ 21 ], abscisic acid ( 9 ) [ 22 ], (+)-dehydrovomifoliol ( 10 ) [ 23 ], grasshopper ketone ( 11 ) [ 24 ], roseoside ( 12 ) [ 25 ], citroside A ( 13 ) [ 23 ], 4′-(6-amino-9 H -purin-9-yl)pentan-2′-one ( 14 ) [ 26 ], seco-( S -Pro- R -Val) (1 5 ) [ 27 ], cyclo-( L -Pro- L -Ala) ( 16 ) [ 28 ], 3-methoxyl-1 H -pyrrole ( 17 ) [ 29 ], cyclo-(Ala-Val) ( 18 ) [ 30 ], indole-3-carboxyl- β -D-glucopyranoside ( 19 ) [ 31 ], uridine ( 20 ) [ 32 ], thymidine ( 21 ) [ 33 ], adenosine ( 22 ) [ 34 ], hypoxanthine ( 23 ) [ 35 ], aurantiamide acetate ( 24 ) [ 36 ], and L -pyroglutamic acid methyl ester ( 25 ) [ 37 ].…”
Section: Resultsmentioning
confidence: 99%
“…The HPLC chromatogram of MLE generated by full-scan diode array detector (PDA) and the structures of identified components were shown in Figure 1A,B, respectively. These compounds have been identified in mulberry leaves and the flavonoids were major components in MLE [25,26]. components with higher peak areas in HPLC (3-5) were compared with commercial standards, and the identities of the compounds were confirmed.…”
Section: The Main Components In Mlementioning
confidence: 92%
“…The HPLC chromatogram of MLE generated by full-scan diode array detector (PDA) and the structures of identified components were shown in Figure 1A,B, respectively. These compounds have been identified in mulberry leaves and the flavonoids were major components in MLE [25,26].…”
Section: The Main Components In Mlementioning
confidence: 99%