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. 2019 Nov 25;8(12):541. doi: 10.3390/plants8120541

Table 2.

UHPLC-DAD-MS/MS data of compounds detected in analyzed extracts.

Peak No. Compound Name Retention Time (min) UV (nm) (M − H) m/z MS2 ions (M + H)−+ m/z MS2 ions Compound Content ug/mg
Extract I 20% EtOH Extract II 60% EtOH Extract III 96% EtOH
1 Monotropeint 2.1 237 389 369, 227, 209b, 183, 137 381 - n.q. n.q. n.q.
2 10-Desacetylasperulosidic acidt 3.7 237 389 227b, 209, 183 381 - n.q. n.q. n.q.
3 p-Hyroxybenzoic acids 5.9 259, 294 153 - 155 - n.q. n.q. n.q.
4 3-O-Caffeoylquinic acids 9.7 217, 241, 300sh, 324 353 191b, 179, 161 355 163b 8.91 ± 0.09 3.72 ± 0.12 0.53 ± 0.03
5 Asperulosidic acidt 14.0 235 431 371, 269, 251b, 165 433 - n.q. n.q. n.q.
6 5-O-Caffeoylquinic acids (Chlorogenic acid) 16.2 219, 241, 299sh, 325 353 191b, 179 355 163b 18.44 ± 0.21 31.51 ± 0.19 40.61 ± 0.12
7 4-O-Caffeoylquinic acids 18.2 217, 241, 300sh, 325 353 191, 179, 173b 355 337, 307, 163b 8.12 ± 0.03 4.75 ± 0.08 1.16 ± 0.02
8 Quercetin 3-O-rhamnoglucoside-7-O-glucosides 23.1 255, 263sh, 353 771 609b, 301 773 627, 611, 465b, 303 3.35 ± 0.10 2.95 ± 0.05 1.50 ± 0.02
9 Quercetin 3-O-rhamnoglucosides (Rutin) 36.9 255, 262sh, 354 609 591, 301b, 179 611 465, 303b 1.08 ± 0.05 2.49 ± 0.03 6.33 ± 0.07
10 Caffeic acid derivative 38.0 254, 299sh, 327 381 207, 191, 179b, 135 383 365, 163b n.q. n.q. n.q.
11 Isorhamnetin 3-O-glucorhamnosides 40.4 259, 260sh, 350 615 609b, 542, 461, 315 617 - n.q. n.q. n.q.
12 3,4-O-Dicaffeoylquinic acids 42.9 239, 300sh, 324 515 353b, 255, 173b 517 499b, 317, 163 n.q. n.q. n.q.
13 3,5-O-Dicaffeoylquinic acids 43.8 240, 299sh, 324 515 353, 233, 191b, 179 517 499b, 147 0.23 +/− 0.02 0.42 +/− 0.08 2.43 +/− 0.11
14 4,5-O-Dicaffeoylquinic acids 47.9 240, 300sh, 325 515 515, 353b, 299, 255, 203 517 499, 335b, 278 n.q. n.q. n.q.

s—comparisons with chemical standard have been made; b—base peak (the most abundant ion in recorded spectrum); sh-shoulder; t—tentative assignment; n.q.—not quantified.