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Table 3 UHPLC-MS of M. buxifolia stem extracts (negative ionization mode)

From: Metabolic fingerprinting, antioxidant characterization, and enzyme-inhibitory response of Monotheca buxifolia (Falc.) A. DC. extracts

S/No

RT (min)

B.Peak (m/z)

Compound name

Comp. class

Mol. formula

Mol. Mass

M. buxifolia stem methanol extract

1

11.128

391.12

Shanzhiside

Iridoid glycoside

C16 H24 O11

527.09

2

11.317

577.13

Apigenin 7-(2″-E-p-coumaroylglucoside)

Flavonoid

C30 H26 O12

145.07

3

11.341

755.20

Kaempferol 3-(2G-glucosylrutinoside)

Flavonoid

C33 H40 O20

641.13

4

11.61

449.10

8-C-Glucopyranosyleriodictylol

Flavonoid

C21 H22 O11

243.05

5

11.672

581.22

(7’R)-(+)-Lyoniresinol 9′-glucoside

Lignan Glycoside

C28 H38 O13

244.90

6

12.216

463.08

8-Hydroxyluteolin 8-glucoside

Flavonoid

C21 H20 O12

567.16

7

12.952

1353.63

Diosgenin 3-[glucosyl-(1- > 4)-[glucopyranosyl-(1- > 6)]-glucopyranosyl-(1- > 4)-rhamnosyl-(1- > 4)-[rhamnosyl-(1- > 2)]-glucoside]

Alkaloid

C63 H102 O31

1354.63

8

13.695

269.10

Idebenone Metabolite (Benzenebutanoic acid, 2,5-dihydroxy-3,4-dimethoxy-6-methyl-)

Phenolic

C13 H18 O6

392.13

9

16.669

221.11

(6S)-dehydrovomifoliol

Terpenoid

C13 H18 O3

159.98

10

21.036

471.34

Lucidumol A

Triterpenoid

C30 H48 O4

353.07

M. buxifolia stem chloroform extract

1

16.63

221.11

(6S)-dehydrovomifoliol

Terpenoid

C29 H42 O5

222.12

2

17.714

356.17

Uplandicine

Alkaloid

C30 H48 O5

357.17

3

20.376

257.15

Cicutoxin

Fatty Alcohol

C29 H46 O4

258.16

4

20.816

461.19

Mangostenone B

Benzopyran

C20 H24 O2

462.20

5

21.814

297.24

cis-9,10-Epoxystearic acid

Lineolic Acid

C16 H32 N6 O5

298.25

6

22.066

339.23

Plastoquinone 3

Isoprenoid quinone

C23 H32 O2

340.24

7

22.164

471.34

Lucidumol A

Triterpenoid

C30 H48 O4

472.35

8

22.2

617.38

3-O-cis-Coumaroyl maslinic acid

Triterpenoid

C39 H54 O6

618.39

  1. RT retention time, B. peak base peak