Table 1.
N | RT | [M+H] | MSn Fragments | Name Suggestion for Structure | Reference |
---|---|---|---|---|---|
1 | 4.48 | 299 | 289, 287, 160 | carajurin | [17,18,19] |
2 | 5.38 | 315 | 313, 289 | 6,7,3′-trihydroxy-5,4′-dimethoxy-flavylium | [18] |
3 | 17.61 | 289 | 205, 188 | 2′-hydroxy-a-naphthoflavone | [20] ID BML00331 |
4 | 24.13 | 289 | catechin | [21] | |
5 | 24.69 | 301 | 289 | 5,7-dimethoxy-4′-hydroxyflavone | |
6 | 25.42 | 289 | epicatechin | [21] | |
7 | 29.98 | 477 | 301, 289 | quercetin-o-gallate | |
8 | 31.12 | 465 | 301 | Quercetin-o-glucoside | [22] |
9 | 32.04 | 540 | 460, 301, 289 | amentoflavone | [23] |
10 | 34.72 | 479 | 301, 279 | isorhamnetin-3-o-glucoside | [24] |
11 | 36.62 | 301 | 279 | chrysoeriol | [25] |
12 | 37.64 | 287 | 279 | kaempferol | [26] |
13 | 39.65 | 463 | 330, 301 | chrysoeriol-o-glucoside | [27] |
14 | 41.24 | 317 | 301, 279 | isorhamnetin | [24] |
15 | 42.99 | 287 | 279 | luteolin | [28,29] |
16 | 45.25 | 303 | 6-hydroxyluteolin | [29] | |
17 | 46.18 | 477 | 328, 301, 279 | cirsimarin | [30,31] |
18 | 47.42 | 617 | 601, 301, 279 | hyperin 6″ gallate | |
19 | 47.64 | 301 | 279 | 6,7,3′,4′-tetrahydroxy-5-metoxy-flavilium | [32] |
20 | 47.94 | 302 | 301, 288, 285 | hispidulin | [29] |
21 | 49.23 | n.i. | |||
22 | 50.31–50.96 | 601 | n.i. | ||
23 | 52.72–54.29 | 577 | 301, 289 | catechin dimer | [29] |
24 | 62.14 | 819 | n.i. | ||
25 | 72.66 | 593 | 421, 399 | feoforbide A | [33] |
n.i.—not identified.