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. 2019 Nov 22;9:17430. doi: 10.1038/s41598-019-54078-1

Table 1.

Secondary metabolites 143 isolated from A. pilosa roots and aerial parts.

No.a Name Exact molecular weight Molecular Formula FCIb
1 pilosanidin A 814.2472 C43H42O16 89.3
2 pilosanidin B 814.2472 C43H42O16 89.5
3 pilosanidin C 828.2629 C44H44O16 89.4
4 pilosanidin D 798.2523 C43H42O15 89.4
5 pilosanidin E 798.2523 C43H42O15 89.2
6 pilosanol A 540.1995 C29H32O10 58.4
7 pilosanol B 526.1829 C28H30O10 77.7
8 pilosanol C 526.1829 C28H30O10 83.1
9 isopilosanol A 540.1995 C29H32O10 85.1
10 isopilosanol B 526.1829 C28H30O10 80.3
11 isopilosanol C 526.1829 C28H30O10 83.3
12 epipilosanol A 540.1995 C29H32O10 58.3
13 epipilosanol B 526.1829 C28H30O10 81.8
14 epipilosanol C 526.1829 C28H30O10 71.5
15 epipilosanol N 498.1526 C26H26O10 84.0
16 agrimonolide 314.1154 C18H18O5 87.7
17 agrimonolide-6-O-Glcc 476.1682 C24H28O10 89.2
18 agrimonolide-6-O-Arafd−6-O-Glc 608.2105 C29H36O14 87.5
19 4-hydroxyagrimonolide 6-O-Glc 492.1632 C24H28O11 88.0
20 desmethylagrimonolide 6-O-Glc 462.1526 C23H26O10 86.9
21 desmethylagrimonolide 4′-O-Glc 462.1526 C23H26O10 89.1
22 5,7-dihydroxy-2-propylchromone 7-O-Glc 382.1264 C18H22O9 82.9
23 5,7-dihydroxy-2-(1-methylethyl) chromone 7-O-Glc 382.1264 C18H22O9 79.3
24 5,7-dihydroxy-2-(1-methylpropyl) chromone 7-O-Glc 396.1420 C19H24O9 84.0
25 5,7-dihydroxy-2-(1-methylethyl)chromone-7-O-[6′′-HMGe]-β-D-glucopyranoside 526.1686 C24H30O13 84.6
26 5,7-dihydroxy-2-(1-methylpropyl)chromone-7-O-[6′′-HMG]-β-D-glucopyranoside 540.1843 C25H32O13 86.9
27 corosolic acid 472.3552 C30H48O4 54.5
28 rosamultin 650.4030 C36H58O10 57.8
29 2-oxopomolic acid 486.3345 C30H46O5 63.4
30 (1β,2α,3β)-1,2,3,19-tetrahydroxyurs-12-en-28-oic acid 504.3451 C30H48O6 65.4
31 (1β,2α)-1,2,19-trihydroxy-3-oxo-urs-12-en-28-oic acid 502.3294 C30H46O6 69.8
32 1β-hydroxy-2-oxopomolic acid 502.3294 C30H46O6 69.8
33 fupenzic acid 484.3189 C30H44O5 65.6
34 maslinic acid 472.3552 C30H48O4 50.0
35 arjunetin 650.4030 C36H58O10 49.8
36 kaempferol-3-O-Glc 448.1006 C21H20O11 73.3
37 cis-tiliroside 594.1373 C30H26O13 75.8
38 trans-tiliroside 594.1373 C30H26O13 75.3
39 apigenin-7-O-Glc 432.1056 C21H20O10 67.4
40 luteolin-7-O-Glc 448.1005 C21H20O11 66.0
41 apigenin-7-O-GlcAf 446.0849 C21H18O11 73.7
42 dihydrokaempferol-3-O-Glc 450.1162 C21H22O11 73.0
43 (2S,3S)-glucodistylin 466.1111 C21H22O12 74.5

aCompounds 1, 2, 6–11 and 16–21 have been reported in a previous study, and 35, 12–15 and 22–43 were isolated in the present study.

bFCI: fresh compound index; cGlc: β-D-glucose; dAraf: α-L-arabinofuranose; eHMG: (S)3-hydroxy-3-methylglutaroyl, fGlcA: β-D-glucuronic acid.