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. 2018 Jun 17;23(6):1468. doi: 10.3390/molecules23061468

Table 1.

UPLC-DAD-ESI-MSn data of detected and identified polyphenolic compounds in extracts of aerial parts of S. viridis.

Compounds Retention Time [min] UV [nm] [M − H] Fragmentation Ions
1 6-O-caffeoylglucose (I) 10.6 324 341 323, 281, 251, 221, 179
2 6-O-caffeoylglucose (II) 12.3 325 341 323, 281, 251, 221, 179
3 5-O-caffeoylquinic acid (chlorogenic acid) a 12.8 325 353 191
4 4-O-caffeoylquinic acid (cryptochlorogenic acid) 13.7 325 353 191, 173, 135
5 caffeoyl-hexoside derivative 18.7 325 537 519, 341, 281, 179
6 luteolin-O-rutinoside 22.1 253, 269, 344 593 285
7 verbascoside a 23.1 330 623 461, 315, 135
8 forsythoside A 24.5 326 623 461, 477, 315, 135
9 isoverbascoside a 25.0 326 623 461, 315, 135
10 lipedoside A 25.8 316 607 461, 443, 315, 297, 135
11 dicaffeoylquinic acid 26.0 328 515 353, 191, 179
12 leucosceptoside A 26.3 328 637 461, 315, 135
13 apigenin-O-hexuronide 26.7 267, 332 445 269, 149
14 methylluteolin-O-hexuronide
(chrysoeriol hexuronide)
27.1 269, 343 475 299, 285, 175
15 rosmarinic acid a 27.7 327 359 197, 179, 161
16 unidentified phenylethanoid 28.4 328 803 641, 461, 443, 315
17 luteolin-O-dihexoside 29.7 255, 360 609 447, 429, 285
18 martynoside 30.3 328 651 505, 475, 457, 329
19 isomartynoside 31.1 328 651 505, 475, 457, 329, 193

a Identified with authentic standards, in bold—the most abundant fragmentation ion.