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. 2021 Apr 30;12:618844. doi: 10.3389/fphar.2021.618844

TABLE 1.

Characterization of the chemical constituents in ARC by ultraperformance liquid chromatography quadrupole time-of-flight tandem mass spectrometry.

Number tR/min Formula ESI-MS ESI-MS/MS ppm Identity References
1 4.88 C22H33NO5 [M + H] + 392.2424 374.2335, 356.2339 −1.8 Hokbusine B Konno et al. (2004)
2 5.08 C24H39NO9 [M + H] + 486.2693 454.2433, 436.2327 −0.9 Mesaconine Sun et al. (2013)
3 5.14 C16H17NO3 [M-H] − 270.1139 162.0584, 135.0498 1.5 Higenamine Kosuge and Yokota (1976)
4 5.54 C23H37NO6 [M + H]+424.2688 406.2587 −1.2 Senbusine A Sun et al. (2013)
5 5.77 C22H35NO4 [M + H] + 378.2633 360.2542, 342.2430 −1.3 Carmichaeline Sun et al. (2013)
6 5.94 C23H37NO5 [M + H] + 408.2738 390.2641 −1.5 Isotalatizidine Sun et al. (2013)
7 6.52 C22H31NO3 [M + H] + 358.2372 340.2268 −1.2 Songorine Sun et al. (2013)
8 6.64 C25H41NO9 [M + H] + 500.2848 450.2492 −1.3 Aconine Yang et al. (2014)
9 6.75 C22H33NO3 [M + H] + 360.2528 342.2434 −1.3 Napelline Yang et al. (2014)
10 7.06 C20H27NO3 [M + H]+ 330.2059 330.2066 −1.3 Hetisine Sun et al. (2013)
11 7.91 C24H39NO8 [M + H] + 470.2742 438.2489, 406.2230 −1.2 Hypaconine Yang et al. (2014)
12 7.98 C24H39NO7 [M + H] + 454.2794 436.2691 −1.1 Fuziline Sun et al. (2013)
13 8.38 C24H39NO6 [M + H] + 438.2845 420.2745, 388.2487 −1 Neoline Sun et al. (2013)
14 8.52 C25H41NO7 [M + H] + 468.2947 418.2598 −1.7 Lycoctonine Yuxin et al. (2016)
15 8.96 C27H41NO8 [M − H] − 506.2760 506.2703 0.2 Deltaline Gardner et al. (1999)
16 9.01 C23H37NO4 [M + H]+ 392.2789 360.2520, 342.2434 −1.4 Sachaconitine Yuxin et al. (2016)
17 9.13 C24H39NO5 [M + H] + 422.2894 358.2376 −1.5 Talatisamine Sun et al. (2013)
18 9.16 C22H33NO2 [M + H] + 344.2578 326.2476 −1.7 Denudatine Sun et al. (2013)
19 9.61 C25H39NO7 [M + H] + 466.2791 434.2536 −1.7 Delbruine Yuxin et al. (2016)
20 9.73 C26H41NO7 [M + H] + 480.2948 462.2826 −1.6 14-Acetylneoline Yuxin et al. (2016)
21 9.87 C25H41NO6 [M + H] + 452.2998 420.2750, 388.2421 −1.8 Chasmanine Sun et al. (2013)
22 10.19 C22H29NO3 [M + H] + 356.2215 356.2224, 296.1606, 139.0203 −1.3 Songoramine Yuxin et al. (2016)
23 10.34 C29H39NO6 [M + H] + 498.2844 480.2753, 462.2637 −1.1 Delavaconitine Csupor et al. (2008)
24 11.06 C27H43NO7 [M + H] + 494.3104 462.2847 −1.6 Delbrusine Yuxin et al. (2016)
25 a 11.78 C31H43NO10 [M + H] + 590.2591 540.2561, 105.0345 −1.4 Benzoylmesaconine Sun et al. (2013)
26 a 12.41 C32H45NO10 [M + H] + 604.3104 572.2846, 554.2734 −1.9 Benzoylaconine Yang et al. (2014)
27 12.6 C27H31NO5 [M + H] + 450.2264 450.2283 −2.3 Ignavine Ochiai and Okamoto (2008)
28 a 12.81 C31H43NO9 [M + H] + 574.3002 542.2738, 510.2468 −1.5 Benzoylhypacoitine Yang et al. (2014)
29 13.35 C33H45NO12 [M + H] + 648.2998 588.2798 −2.4 Beiwutine Yang et al. (2014)
30 13.72 C33H45NO11 [M + H] + 632.3055 572.2863, 540.2539 −1.6 Mesaconitine Sun et al. (2013)
31 13.91 C33H45NO9 [M + H] + 600.3156 568.2886, 131.0491 −1.8 Isodelphinine Katsui (2006)
32 14.21 C34H47NO12 [M + H] + 662.3163 602.2986 −1.1 10-OH-aconitine Yuxin et al. (2016)
33 14.83 C34H47NO11 [M + H] + 646.3216 586.3030, 368.1870 −0.9 Aconitine Sun et al. (2013)
34 14.83 C33H45NO10 [M + H] + 616.3101 556.2906, 524.2650, 338.1758 −2.4 Hypaconitine Sun et al. (2013)
35 14.94 C32H45NO8 [M + H] + 572.3207 572.3221, 484.2699, 382.2020 −1.8 14-O-Anisoylneoline Yuxin et al. (2016)
36 15.26 C34H47NO9 [M + H] + 392.2424 596.3221, 508.2669, 570.2681, 538.2787 −1.8 Chasmaconitine Yang et al. (2014)
37 15.51 C34H47NO10 [M + H] + 630.3259 510.2822, 352.1917 −2.2 Deoxyaconitine Sun et al. (2013)
38 15.85 C41H43NO12 [M + H] + 742.2845 620.2643 −1.7 Delgrandine Yuxin et al. (2016)
39 16.21 C35H49NO9 [M + H] + 628.3466 596.3146 −2.2 Vilmorrianine C Yuxin et al. (2016)
40 16.95 C29H37NO5 [M + H] + 480.2733 448.2468, 420.2493, 145.1025 −2.4 Cytochalasin B Evidente et al. (2003)
41 a 17.56 C27H28N2O4 [M − H] − 443.1981 443.0180, 59.0223 1.1 Aurantiamide acetate Songue et al. (2012)
42 23.28 C14H28O2 [M − H] − 227.2023 227.2020, 183.0452 3.2 Myristic acid Bianco et al. (2020)
43 24.38 C18H32O2 [M-H] − 279.2342 279.2339 4.5 Linoleic acid Bianco et al. (2020)
a

Identified by comparison with standards.