1989
DOI: 10.1007/bf00597667
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Phenolic compounds of the bark of Syringa vulgaris

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Cited by 9 publications
(17 citation statements)
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“…The phytochemical analysis of S. vulgaris bark, fruit, flower and leaf infusions and ethanolic extracts was performed using a HPLC-DAD-MS/MS method, which allowed for the identification or partial identification of 64 compounds (Table 1 and Figure 1 ) from the following groups: phenylethanoids (compounds 27 , 31 , 36 , 39 , and 42 ), rare phenylethanoids esterified with an oleoside 11-methyl ester (compounds 43 , 49 , 50 , and 61 ), flavonoids (compounds 32 , 33 , and 35 ), other phenolic compounds ( 1 – 3 , 5 – 14 , 17 , 18 , and 24 ), lignans (compounds 21 and 37 ), iridoids (compounds 34 and 41 ), secoiridoids (compounds 4 , 15 , 16 , 20 , 26 , 28 - 30 , 38 , 40 , 44 – 46 , 48 , 51 – 57 , 60 , 62 , and 63 ), together with eight unknown compounds. Compounds 1 , 2 , 5 , 7 , 14 – 16 , 27 – 29 , 34 , 36 , 38 , 41 , 43 – 46 , 48 – 50 , 52 – 54 , 61 were previously isolated as pure compounds from S. vulgaris leaves, flowers, and bark (Kurkin et al, 1989 , 1990 ; Damtoft et al, 1995 ; Kikuchi et al, 2010 ; Dudek et al, 2017 ). However, this is a first comprehensive phytochemical analysis of a broad range of compounds from different parts of the plant.…”
Section: Resultsmentioning
confidence: 99%
“…The phytochemical analysis of S. vulgaris bark, fruit, flower and leaf infusions and ethanolic extracts was performed using a HPLC-DAD-MS/MS method, which allowed for the identification or partial identification of 64 compounds (Table 1 and Figure 1 ) from the following groups: phenylethanoids (compounds 27 , 31 , 36 , 39 , and 42 ), rare phenylethanoids esterified with an oleoside 11-methyl ester (compounds 43 , 49 , 50 , and 61 ), flavonoids (compounds 32 , 33 , and 35 ), other phenolic compounds ( 1 – 3 , 5 – 14 , 17 , 18 , and 24 ), lignans (compounds 21 and 37 ), iridoids (compounds 34 and 41 ), secoiridoids (compounds 4 , 15 , 16 , 20 , 26 , 28 - 30 , 38 , 40 , 44 – 46 , 48 , 51 – 57 , 60 , 62 , and 63 ), together with eight unknown compounds. Compounds 1 , 2 , 5 , 7 , 14 – 16 , 27 – 29 , 34 , 36 , 38 , 41 , 43 – 46 , 48 – 50 , 52 – 54 , 61 were previously isolated as pure compounds from S. vulgaris leaves, flowers, and bark (Kurkin et al, 1989 , 1990 ; Damtoft et al, 1995 ; Kikuchi et al, 2010 ; Dudek et al, 2017 ). However, this is a first comprehensive phytochemical analysis of a broad range of compounds from different parts of the plant.…”
Section: Resultsmentioning
confidence: 99%
“…alashanensis [44] 120 O -[ β -D-xylopyanosy (1–6) β -D-glucopyranosyl]-7-hydroxycoumarinroots and stems S. pinnatifolia var. alashanensis [44] 121 Syringfghanosideleaves S. afghanica [13] 122 Astragalinbark S. vulgaris [48] 123 Kaempferol-3, 7- α -L-dirhamnosideflowers and leaves S. pubescens [3] 124 Kaempferol-3- β -D-glucoside-7- α -L-dirhamnosideflowers and leaves S. pubescens [3] 125 Kaempferol-3- O -rutinosideflowers S. vulgaris [49] 126 Luteolinleaves S. afghanica [13] 127 Rutinleaves S. vulgaris [49,50] 128 Rhoifolinleaves S. afghanica [13] 129 Guai-9-en-4 β -olroots and stems S. pinnatifolia var. alashanensis [37] 130 14, 15-dinorguai-1, 11-dien-9, 10-dioneroots and stems S. pinnatifolia var.…”
Section: Introductionmentioning
confidence: 99%
“…In spite of the potential pharmacological activities of lilac, only a few papers can be found describing the chemical composition of the plant. Available literature focuses mainly on the phenolic profile of the bark and leaf (Ahmad et al, 1995;Birkofer et al, 1968;Damtoft et al, 1995;Kurkin et al, 1989Kurkin et al, , 1992b. A limited number of papers can be found on the phytochemical composition of the other members of Syringa genus, such as S. oblata (Nenadis et al, 2007), S. afghanica (Takenaka et al, 2002), S. pubescens (Deng et al, 2010) and S. reticulate (Bi et al, 2011;Machida et al, 2002).…”
Section: Introductionmentioning
confidence: 99%
“…Based on these works the main phenolics in Syringa species are phenylpropanoids and iridoid-glycosides, such as acteoside (syn. verbascoside) and oleuropein (Bi et al, 2011;Birkofer et al, 1968;Kurkin et al, 1989Kurkin et al, , 1990Su et al, 2015).…”
Section: Introductionmentioning
confidence: 99%