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. 2015 Dec 11;20(12):22202–22219. doi: 10.3390/molecules201219845

Table 1.

Compounds identified in the Fraxinus angustifolia extract used in this study.

Peak Compounds Rt (UV) [M − H] MS/MS
1 Salidroside 16.60 299 179,119
2 Hydroxycinnamic acid derivative 16.92 487 295, 179, 135
3 Oleoside 19.70 389 371, 345, 209, 179
4 Oleoside 11-methyl ester 22.63 403 223, 179
5 Hydroxycinnamic acid derivative 21.75 369 207, 192, 179
6 Verbascoside 31.45 623 461, 315, 251
7 Nuzhenide isomer 31.75 685 523, 453, 421, 299, 223
8 Nuzhenide 33.28 685 523, 453, 421, 299, 223
9 Nuzhenide isomer 34.72 685 523, 453, 421, 299, 223
10 1-O-β-d-Glucosylformoside 36.03 685 523, 453, 385, 299, 223
11 Nuzhenide derivative 37.01 727 685, 565, 523, 453, 341, 299
12 Excelside B 37.61 685 565, 361, 291, 260
13 GL3 isomer * 41.06 1071 909, 685, 523, 385
14 GL3 isomer * 41.45 1071 909, 771, 685, 609, 421
15 GL3 42.20 1071 909, 771, 685, 453, 385
16 GL3 isomer * 43.36 1071 909, 685, 478, 361
17 Nuzhenide di (11-methyloleoside) 44.96 1457 1157, 1071, 934, 771, 685
18 GL5 isomer 48.70 909 771, 747, 523, 361, 259
19 GL5 isomer 49.77 909 771, 747, 645, 523, 361

* Some of GL3 isomers could correspond to nuzhenide 11-methyloleoside.