International Journal of Analytical Chemistry / 2022 / Article / Tab 1 / Research Article
Comparison of the Saponins in Three Processed American Ginseng Products by Ultra-High Performance Liquid Chromatography-Quadrupole Orbitrap Tandem Mass Spectrometry and Multivariate Statistical Analysis Table 1 Compounds identified from American ginseng by natural drying, steam drying, and vacuum freeze-drying.
No. Rt (min) Identification Formula Detected mass (Da) Mass error (ppm) 1 5.67 Vina-ginsenoside R4 C48 H82 O19 1007.5457a 2.5 2 9.04 Notoginsenoside R1 C47 H80 O18 977.5346a 1.9 3 10.03 Ginsenoside Rg1 C42 H72 O14 845.4914a 1.2 4 10.41 Ginsenoside Re C48 H82 O18 991.5504a 2.1 5 10.73 24 (S)-pseudo-ginsenoside F11 C42 H72 O14 845.4922a 2.1 6 11.45 Malonyl-ginsenoside Rg1 C45 H74 O17 885.4867b 1.6 7 11.51 Malonyl-ginsenoside Re C51 H84 O21 1031.5457b 2.4 8 12.69 20 (S)-notoginsenoside R2 C41 H70 O13 815.4819a 2.6 9 13.47 Ginsenoside F5 C41 H70 O13 815.4814a 2.0 10 13.85 Acetyl-Rg1 C44 H74 O15 887.5024a 1.6 11 14.80 Pseudo-RT2 C41 H70 O14 785.4661b 4.1 12 15.26 24 (R)-pseudo-ginsenoside F11 C42 H72 O14 845.4918a 1.6 13 15.72 Notoginsenoside R4 /Ginsenoside Ra3 C59 H100 O27 1285.6464a 1.6 14 16.46 Ginsenoside Rh1 C36 H62 O9 683.4391a 2.2 15 16.61 20 (S)-ginsenoside Rg2 C42 H72 O13 829.4971a 1.9 16 16.89 20 (R)-ginsenoside Rg2 C42 H72 O13 829.4974a 2.3 17 17.01 Ginsenoside Rb1 C54 H92 O23 1153.603a 1.6 18 17.06 Malonyl-ginsenoside Rb1 /Isomer C57 H94 O26 1193.5983b 1.8 19 17.13 Ginsenoside Rc C53 H90 O22 1123.5920a 1.2 20 17.20 Ginsenoside Ro C48 H76 O19 955.4933b 2.6 21 17.27 Malonyl-ginsenoside Rc C56 H92 O25 1163.5883b 2.4 22 17.29 Malonyl-ginsenoside Rb2 C56 H92 O25 1163.5892b 3.2 23 17.36 Ginsenoside Rb2 C53 H90 O22 1123.5923b 1.5 24 17.59 Ginsenoside Rb3 C53 H90 O22 1123.5924a 1.6 25 17.66 Malonyl-ginsenoside Rb3 C56 H92 O25 1163.5878b 2.0 26 17.73 Pseudo-RT1 C47 H74 O18 971.4800a 5.9 27 17.84 Ginsenoside Rd C48 H82 O18 991.5506a 2.3 28 18.07 Chikusetsusaponin IVa C42 H66 O14 793.4396b 2.0 29 18.10 Malonyl-ginsenoside Rd C51 H84 O21 1031.5458b 2.5 30 18.14 Gypenoside XVII C48 H82 O18 991.5502a 1.9 31 18.40 Pseudo-RC1 C50 H48 O19 1033.5521a 6.6 32 18.63 Quinquefolium III C50 H48 O19 1033.5529a 5.8 33 18.80 Ginsenoside Rg6 C42 H70 O12 811.4810a 4.8 34 18.90 Ginsenoside Rg4 C42 H70 O12 811.4807a 5.2 35 19.24 Ginsenoside F2 C42 H72 O13 829.4971a 1.9 36 19.58 20 (S)-ginsenoside Rg3 C42 H72 O13 829.4976a 2.5 37 19.63 Ginsenoside Rk3 C36 H60 O8 665.4231a 5.9 38 19.79 Ginsenoside Rh4 C36 H60 O8 665.4233a 5.6 39 20.01 Zingibroside R1 C42 H66 O14 839.4382a 5.1 40 20.27 20 (R)-ginsenoside Rg3 C42 H72 O13 829.4982a 3.3 41 20.34 20 (S)-ginsenoside Rs3 C44 H74 O14 871.5015a 5.3 42 20.60 Calenduloside E C36 H56 O9 677.3869a 5.5 43 20.68 20 (R)-ginsenoside Rs3 C44 H74 O14 871.5014a 5.3 44 20.88 Ginsenoside Rk1 C42 H70 O12 811.4859a 1.2 45 20.92 Ginsenoside Rg5 C42 H70 O12 811.4868a 2.3 46 21.19 20 (S)-ginsenoside Rh2 C36 H62 O8 667.4391a 5.4 47 21.42 20 (R)-ginsenoside Rh2 C36 H62 O8 667.4393a 5.1 48 21.62 Ginsenoside Rs5 C44 H72 O13 853.4913a 4.7 49 21.85 Ginsenoside Rs4 C44 H72 O13 853.4913a 4.7 50 23.18 Ginsenoside Rk2 C36 H60 O7 649.4276a 6.9 51 23.33 Ginsenoside Rh3 C36 H60 O7 649.4294a 4.2