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. 2019 Jan 25;14(1):e0211237. doi: 10.1371/journal.pone.0211237

Table 4. Retention time, UV spectrum, mass, molecular formula, chemical class and plants species in which compounds were detected of active peaks with relative intensity of masses higher than 20000 and were positively correlated to EC90.

Peak Ret
(min)
UV [M-H]- Molecular formula MS/MS Class Compounds Plants
1 1.1 --- 665.2114 --- --- Unknown Unknown H_brevi; A_latis; L_canes; V_cymos; H_mutab; M_latif
2 2.0 --- 389.1076 C16H22O11 389: 227 (C10H11O6); 209 (C10H9O5); 183 (C9H11O4) Iridoid Hexosyl iridoid derivative D_kuntz
3 3.0 --- 389.1080 C16H22O11 389: 227 (C10H11O6); 209 (C10H9O5); 183 (C9H11O4) Iridoid Hexosyl iridoid derivative D_kuntz
4 4.7 --- 363.1297 C15H23O10 363:201(C9H13O5) Iridoid Hexosyl iridoid derivative A_hirta
5 6.5 --- 345.1191 C15H22O9 345: 207 (C11H11O4); 189 (C11H9O3); 183 (C9H11O4) Iridoid Hexosyl iridoid derivative A_hirta
6 6.6 --- 345.1190 C15H22O9 345: 207 (C11H11O4); 189 (C11H9O3); 183 (C9H11O4) Iridoid Hexosyl iridoid derivative A_hirta
7 9.0 301/322 353.0891 C16H18O9 353: 191 (C7H11O6) Phenylpropanoid chlorogenic acid I_chili; A_latis; S_hispi; D_kuntz; C_punct; V_cymos; M_latif
8 10.4 --- 413.1085 C18H22O11 413: 371 (C16H19O10); 251 (C12H11O6); 191 (C10H7O4) Iridoid Asperuloside D_kuntz
9 11.5 --- 405.1401 C17H26O11 405: 387 (C17H23O10); 243 (C11H15O6); 225 (C11H13O5) Iridoid Sanshiside methyl ester L_canes
10 11.5 268 633.0719 C27H22O18 633: 463 (C20H15O13); 301 (C14H5O8); 275 (C13H7O7) Hydrolized tannin Corilagin S_hispi
11 12.6 268 951.0787 C41H28O27 951: 933(C41H25O26); 765 (C34H21O21); 463 (C20H15O13); 301 (C14H5O8); 275 (C13H7O7) Hydrolized tannin Geraniin S_hispi
12 12.8 301/327 515.1180 C25H24O12 515: 191 (C7H11O6); 179 (C9H7O4) Phenylpropanoid 1,3 Dicaffeoylquinic I_chili; A_latis
13 16.0 281/344 463.0859 C21H20O12 463: 301 (C15H9O7) Flavonoid Isoquercitrin A_hirta
14 16.4 282 463.0900 C21H20O12 --- Flavonoid Flavanone derivative A_hirta; C_punct
Peak Ret
(min)
UV [M-H]- Molecular formula MS/MS Class Compounds Plants
15 17.4 270/345 739.2096 C33H39O19 --- Flavonoid Flavonol-hexosyl-dideoxyhexosyl T_form; V_cymos
16 17.9 270/344 477.1059 C22H22O12 477: 314 (C16H10O7); 299 (C15H7O7) Flavonoid Isorhamnetin-O-glucoside A_hirta
17 18.0 270/346 461.0740 C21H18O12 461: 285 (C15H9O6) Flavonoid Kaempferol-O-glucuronide L_canes; A_hirta; C_punct; V_cymos
18 19.1 296/327 623.1958 C29H36O15 623: 461 (C20H29O12); 315 (C14H19O8); 179 (C9H7O4); 161 (C9H5O3) Phenylpropanoid Verbascosideo L_canes; H_serra
19 19.1 301/327 515.1190 C25H24O12 515: 191 (C7H11O6); 179 (C9H7O4); 173 (C7H9O5) Phenylpropanoid 3,4 Dicaffeoylquinic I_chili; A_latis; C_punct; V_cymos
20 19.8 301/327 515.1193 C25H24O12 515: 191 (C7H11O6); 179 (C9H7O4) Phenylpropanoid 3,5 Dicaffeoylquinic I_chili; A_latis; C_punct; V_cymos
21 19.9 283/343 593.1489 C27H30O15 593: 285 (C15H9O6) Flavonoid Kaempferol-O-rutinoside I_chili; S_hispi; D_kuntz; H_mutab; H_brevi; C_acule
22 20.0 270 419.0970 C20H20O10 419: 179 (C9H7O4) Unknown Unknown H_serra
23 20.3 290/327 623.1973 C29H36O15 623: 461 (C20H29O12); 315 (C14H19O8); 179 (C9H7O4); 161 (C9H5O3) Phenylpropanoid Isoverbascosideo L_canes
24 20.5 266/338 445.0753 C21H18O11 445: 269 (C15H9O5) Flavonoid Apigenin-O-glucuronide L_canes
Peak Ret
(min)
UV [M-H]- Molecular formula MS/MS Class Compounds Plants
25 20.6 292/326 359.0760 C18H16O8 359: 197 (C9H9O5); 179 (C9H7O4); 161 (C9H5O3) Phenylpropanoid Rosmarinic acid H_mutab; H_brevi
26 23.5 300/326 307.0462 C14H12O8 --- Phenylpropanoid Unknown E_panic
27 23.6 287/330 717.1420 C36H30O16 717: 519 (C27H19O11); 339 (C18H11O7); 321 (C18H9O6) Unknown Unknown H_mutab; H_brevi
28 28.2 --- 809.4308 C42H66O15 809: 603 (C35H55O8) Triterpene saponin quinovic acid derivative T_formo
29 28.7 300/326 403.1380 C21H24O8 403: 359 (C20H23O6); 241 (C12H17O5); 197 (C11H17O3); 179 (C9H7O4) Brevipolide Dihydro-Brevipolide C H_brevi
30 29.5 281/346 359.0759 C18H16O8 359: 329 (C16H9O8); 301 (C15H9O7); 286 (C14H8O7); Flavonoid 5,6,3'-trihydroxy-3,7,4'-trimethoxyflavone H_brevi
31 30.4 --- 955.4908 C48H76O19 --- Triterpene saponin Calenduloside derivative A_latis
32 30.6 --- 793.4358 C35H55O7 793:587 () Triterpene saponin --- T_formo; V_cymos
33 30.8 300/313 387.1445 C21H24O7 403: 343 (C20H23O5); 241 (C12H17O5); 197 (C11H17O3); 179 (C9H7O4) Brevipolide Dihydro-Brevipolide F H_brevi
34 31.8 --- 955.4911 C48H76O19 --- Triterpene saponin Calenduloside H I_chili; A_latis
35 32.6 --- 939.4971 C48H76O18 --- Triterpene saponin Triterpene saponin derivative I_chili; A_latis
36 34.8 --- 793.4362 C42H66O14 --- Triterpene saponin Ladyginoside B I_chili
37 36.0 --- 777.4416 C42H66O13 --- Triterpene saponin Triterpene saponin derivative I_chili; A_latis