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Table 3 Compounds identified in the THF BC extract with negative electrospray ionization (ESI-) MS analysis

From: Alpha-glucosidase inhibitory activities of astilbin contained in Bauhinia strychnifolia Craib. stems: an investigation by in silico and in vitro studies

S.No

RT

Name of the compound

Molecular Formulae

m/z

Peak area

(%)

1

2.626

2-Amino-3-methyl-1-butanol

C5H13NO

104

1.79

2

3.099

Methyl β-D-glucopyranoside

C7H14O6

195

8.98

3

3.51

6-(2-aminoethyl)benzene-1,2,3,4,5-pentol

C8H11NO5

202

2.91

4

9.063

2'',3''-Di-O-p-coumaroylafzelin

C39H32O14

725

0.79

5

10.155

ent-Epicatechin(4α- > 8)catechin

C30H26O12

579

0.60

6

10.434

Ent-epicatechin-(2α- > 7,4α- > 8)-epicatechin 3-galactoside

C36H34O17

739

1.38

7

10.898

Ent-epicatechin-(2α- > 7,4α- > 8)-epicatechin 3-galactoside

C36H34O17

739

1.34

8

11.213

3-O-β-D-Galactopyranosylproanthocyanidin A5'

C36H34O17

739

1.34

9

11.877

2-oxalobenzoic acid

C9H6O5

195

0.66

10

12.031

Prenyl caffeate

C14H16O4

249

0.95

11

12.143

Prenyl caffeate

C14H16O4

249

2.38

12

12.653

5,7,3′,5′-Tetrahydroxyflavanone

C15H12O7

305

3.61

13

12.898

5,7,3′,5′-Tetrahydroxyflavanone

C15H12O7

305

7.88

14

13.39

Quercetin

C15H10O7

303

16.22

15

13.918

Fustin

C15H12O6

289

3.16

16

14.339

Eriodictyol

C15H12O6

289

2.61

17

16.717

Fisetin

C15H10O6

287

1.84

18

17.295

C16 Spinganine

C16H35NO2

274

27.23

19

17.588

Hexosylsphingosine

C24H47NO8

478

0.56

20

18.661

Dehydrophytospingosine

C18H37NO3

316

0.34

21

19.356

Phytospingosine

C18H39NO3

318

1.16

22

20.643

Lauroyl diethanolamide

C16H33NO3

288

0.78

23

21.621

Coniferyl benzoate

C17H16O4

285

1.70

24

22.378

2',6'-Dihydroxy-4'-methoxy-3'-methyldihydrochalcone

C17H18O4

287

0.31

25

33.356

Tridodecylamine

C36H75N

522

1.62

26

34.975

dimethyldistearylamine

C38H79N

551

0.33