Table 4 Dereplication table of the significant and highly correlated putatively active metabolites arranged according to their P-values.

From: Application of metabolomics and molecular networking in investigating the chemical profile and antitrypanosomal activity of British bluebells (Hyacinthoides non-scripta)

m/z

Rt

Identification/molecular formula

Earlier reported biological source

Reported activity (ref.)

Probability P ≤ 0.05

1225.5862

[M + H]+

15.63

scillascilloside E2

C57H92O28

Scilla scilloides

cytotoxic41

3.84E-11

457.3313

[M − H]

15.65

3-dehydro-15-deoxoeucosterol

C29H44O4

Scilla scilloides

antiinflammatory44

3.33E-11

1093.5438

[M + H]+

15.63

mycaloside F

deapioplatycodin D

C52H84O24

Mycale laxissima

Platycodon grandiflorum

antiviral47

1.61E-09

1269.5766

[M − H]

15.64

C51H98O35

C58H94O30

No match

 

8.61E-09

1251.6031

[M − H]

12.61

ardisicrenoside C cauloside H

C59H96O28

cf. with scillanoside L-2

C59H94O28

Ardisia crenata Caulophyllum thalictroides

Scilla scilloides

cytotoxic48,49

8.43E-08

1267.5977

[M − H]

17.15

soyasaponin A1

C59H96O29

Impatiens siculifer

antiinflamatory50

1.51E-05

1283.5914

[M + formate-H]

15.73

zingiberenin G

platycoside G2

scillanoside L1

C59H96O30

Platycodon grandiflorum

Dioscorea zingiberensis

Scilla scilloides

cytotoxic41

4.51E-04

1237.5866

[M − H]

15.73

scillanoside L-1

C58H94O28

Scilla scilloides

cytotoxic41

6.27E-04

1239.6016

[M+H]+

15.74

scillanoside L-1

C58H94O28

Scilla scilloides

cytotoxic41

5.02E-04

563.1411

[M − H]

7.35

flavonoid glycosides

anthraquinone glycosides

C26H28O14

widely distributed

cytotoxic51

6.47E-04

1415.6346

[M − H]

15.55

platycoside G1

C64H104O34

Platycodon grandiflorum

weak cytotoxic52

1.40E-02

1369.6269

[M − H]

15.56

heteropappussaponin 7 polygalacin D2

C63H102O32

Heteropappus altaicus Platycodon grandiflorum

antiproliferative53

1.93E-02