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Table 3 Compounds recognized in methanol fruit extract of H. umbellatta

From: Phytochemical screening, gas chromatograph/mass spectrometer (GCMS) analysis and molecular toxicological potential of Hunteria umbellata aqueous fruit extract against Staphylococcus aureus in accessory gene regulators (AGRs)

Peak No

Phyto-compounds

Molecular Formula

Retention Time (min.)

Molecular Weights (gmol−1)

Area Composition (%)

Quality (%)

Chemical Structure

1

Cuparene

C15H22

10.42

202.33

6.63c

95

2

1-Methylenespiro[2.4]heptan-4-one

C8H10O

11.90

122.16

1.13

43

3

Tetradecanoic acid

C14H28O2

12.93

228.37

6.21d

96

4

2-Butynedioic acid, di-2-propenyl ester

C10H12O4

13.07

196.20

2.08

49

5

2-Pentadecanone, 6,10,14-trimethyl

C18H36O

13.80

268.48

16.08b

96

6

Butyl octyl phthalate

C20H30O4

14.07

334.45

2.19

86

7

7-Hexadecene, (Z)-

C16H32

14.13

224.42

2.59

97

8

Camphor

C10H16O

14.56

152.23

1.62

42

9

Methyl 14-methylpentadecanoate

C17H34O2

14.60

270.45

3.26

97

10

n-Hexadecanoic acid

C16H32O2

15.01

256.42

25.24a

99

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11

1-Octadecene

C18H36

16.10

252.50

4.73

97

12

Methyl linoleate

C19H34O2

16.21

294.47

1.10

95

13

Trans-13-Octadecenoic acid, methyl ester

C19H36O2

16.27

296.49

1.41

99

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14

Bromoacetic acid, octadecyl ester

C20H39BrO2

16.34

391.40

1.76

49

15

Cyclohexaneethanol, 4-methyl-.beta.-methylene-, trans-

C12H24O

16.66

184.32

5.80

45

16

Octadecanoic acid

C18H36O

16.81

284.48

2.31

70

17

1-Octadecene

C18H36

17.23

252.50

2.45

97

18

9-Octadecenoic acid, (E)-

C18H34O2

17.67

282.50

5.70e

83

19

1-Hexadecanol, 2-methyl-

C17H36O

18.51

256.47

5.27

66

20

2 (Isobutoxycarbonyl)benzoic acid

C12H14O4

20.75

222.24

2.42

46

  1. abcde: The top 5 abundant phyto-compounds in descending order (highest to smallest)