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. 2019 Nov 27;24(23):4327. doi: 10.3390/molecules24234327

Table 1.

Identification and quantification of phenolic compounds from S. africana, S. officinalis ‘Icterina’ and S. mexicana aqueous extracts.

RT UVmax [M − H] MS 2 Main Fragments Probable Compound S. afr * S. ict * S. mex *
1.5 275 149 103, 87, 131, 59 2,4-DimethylBA 3.4 ± 0.2 4.7 ± 0.1 5.1 ± 0.1
1.7 205 191 111, 173 Quinic Ac D 0.40 ± 0.05 D
3.6 280 197 179, 73, 153 Danshensu 6.5 ± 0.3 D 3.5 ± 0.1
4.2 278 315 153 Protoc Ac Hex - - D
5.0 290 sh, 324 353 191, 179, 135 cis-3-O-CQA - - 3.8 ± 0.0
5.3 290, 327 311 149, 179 Caftaric Ac - - 3.50 ± 0.04
8.3 313 295 163 p-Coum Ac Pent - - 0.03 ± 0.01
8.8 290 sh, 325 353 191 trans-5-O-CQA - - 1.70 ± 0.06
9.4 ND 325 163, 119 Caff Hex - - 0.3 ± 0.0
9.5 290 sh, 325 353 173, 179, 191 4-O-CQA - - 2.5 ± 0.3
9.7 290 sh, 323 179 135 Caff Ac 2.3 ± 0.1 2.50 ± 0.04 0.9 ± 0.1
11.7 271 1077 358, 179, 296, 494 Galotannin Der D - -
12.1 271, 336 593 473, 503, 353 Api-6-C-Glc-7-O-Glc - 3.5 ± 0.1 -
12.3 289, 329 295 207, 179, 133, 135 Caff Malic Ac - - 1.00 ± 0.03
12.6 286, 320 313 269, 179, 135 SA F - 2.7 ± 0.2 D
13.1 291, 311 637 351, 285, 193 Ferulic Ac Der - 0.6 ± 0.1 -
13.5 274 571 527, 483, 439, 373 YA E (isomer 1) 3.8 ± 0.3 - 4.4 ± 0.2
13.9 256, 267 sh, 345 447 327, 357 Lut-C-Hex - - 4.1 ± 0.2
13.9 281, 345 477 301, 373, 343, 397 Hydroxy-Lut-GlcA D 2.90 ± 0.05 -
14.1 276 571 527, 439, 553, 483 YA E (isomer 2) 5.2 ± 0.7 - -
14.3 276 597 579, 355, 312, 295, 197, 179 YA F 8.7 ± 0.9 - -
14.7 274 571 527, 509, 553, 483, 285 YA E (isomer 3) 18.3 ± 0.9 - 2.80 ± 0.01
14.8 267, 345 621 351, 269 Api-diGlcA - D -
15.1 276 555 313, 357 SA K 3.9 ± 0.3 - -
15.4 274 571 527, 553, 509, 329 YA E (isomer 4) D - -
15.6 235, 275, 320 539 297, 359, 495, 279 YA D (isomer 1) D - -
15.9 280, 333 461 285 Scut-O-GlcA - 9.7 ± 0.2 -
15.9 277 539 341, 253, 315, 359 YA D (isomer 2) 2.4 ± 0.2 - 3.5 ± 0.1
16.1 255, 266 sh, 345 461 285 Lut-7-O-GlcA 18.7 ± 1.2 18.2 ± 0.4 -
16.5 268 571 527, 409 YA E (isomer 5) 30.8 ± 1.7 - -
17.2 278 717 519, 475, 537, 339 SA B (isomer 1) - - 1.50 ± 0.02
17.3 279 571 527, 553, 329 YA E (isomer 6) 15.4 ± 0.84 - -
17.6 283 719 359, 539, 521, 341 Sag Ac (isomer 1) 6.0 ± 0.3 9.1 ± 0.4 1.20 ± 0.01
18.1 269, 329 431 269 Api Hex - 1.70 ± 0.03 -
18.3 238, 341 607 299, 284 Chrys Rut - - D
18.4 267, 337 445 269, 175 Api-O-GlcA 4.6 ± 0.2 32.8 ± 0.5 -
18.6 270 717 555, 519, 475, 357 SA B (isomer 2) 3.2 ± 0.2 3.3 ± 0.2 -
18.7 284, 330 sh 609 301 Hesperidin - - 0.50 ± 0.03
19.0 290 sh, 328 359 161, 179, 197, 223 RA 77.0 ± 3.6 52.7 ± 0.5 29.4 ± 0.6
19.2 282 sh, 327 537 493, 295 Caff RA (isomer 1) 3.0 ± 0.2 - -
19.5 285 sh, 305 537 493, 295 Caff RA (isomer 2) 14.2 ± 1.5 - 1.0 ± 0.1
19.8 278 719 521, 341, 359 Sag Ac (isomer 2) - - 2.2 ± 0.1
21.4 285sh, 330 537 456, 493, 375, 359 Caff RA (isomer 3) 2.5 ± 1.0 - -
Sum 231.6 ± 7.5 144.1 ± 2.7 72.8 ± 0.7
Total Phenolic Content 1 350.6 ± 14.9 229.0 ± 44.0 158.9 ± 38.0

Mean values ± S.D.; * Values are expressed as μg/mg extract; 1 Determined by Folin–Ciocalteu assay and expressed as µg of gallic equivalents per mg of extract; D—Detected; Ac—Acid; Api—Apigenin; BA—Benzoic acid; Caff Ac—Caffeic acid; Caff—Caffeoyl; CQA—Caffeoylquinic acid; Chrys—Chrysoeriol; Coum—Coumaroyl; D—Detected; Der—Derivative; Glc—Glucoside; GlcA—Glucuronide; Hex—Hexoside; Lut—Luteolin; ND—Not determined; Pent—Pentoside; Protoc—Protocatechuic; Rut—Rutinoside; RA—Rosmarinic acid; RT—Retention time; Sag—Sagerinic; SA—Salvianolic acid; S. afrS. africana; S. ictS. officinalis ‘Icterina’; S. mexS. mexicana; Scut—Scutellarein; sh—shoulder; UV – Ultraviolet; YA—Yunnaneic acid.