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Table 2 Chemical constitutes of Aspergillus nidulans extract separated by GC–MS

From: Dual anticancer activity of Aspergillus nidulans pigment and Ionizing γ-Radiation on human larynx carcinoma cell line

RT

Chemical name

Formula

Peak area (%)

5.91

Dimethylsulfoxonium formylmethylide

C4H8O2S

10.66

17.71

Dodecanoic acid, methyl ester

C13H26O2

0.50

22.11

Methyl tetradecanoate

C15H30O2

0.91

26.21

Hexadecanoic acid, methyl ester

C17H34O2

21.50

27.53

Hexadecanoic acid

C16H32O2

5.12

28.18

5-(7a-Isopropenyl-4,5-dimethyl-oct ahydroinden-4-yl)-3-methyl-penta-2,4-dien-1-ol

C20H32O

0.73

29.26

9,12-Octadecadienoic acid (Z,Z)-, methyl ester

C19H34O2

8.25

29.39

9-Octadecenoic acid, methyl ester, (E)

C19H36O2

17.39

29.50

9-Octadecenoic acid, methyl ester, (E)-

C19H36O2

6.15

29.87

Octadecanoic acid, methyl ester

C19H38O2

10.53

30.18

cis-5,8,11,14,17-Eicosapentaenoic acid

C20H30O2

0.76

30.51

9-Octadecenoic acid (Z)-

C18H34O2

1.34

30.93

9-Octadecenoic acid (Z)

C18H34O2

1.40

33.21

Eicosanoic acid, methyl ester

C21H42O2

1.15

34.79

Ethanol, 2-(9-octadecenyloxy)-, (Z)-

C20H40O2

0.64

36.35

Docosanoic acid, methyl ester

C23H46O2

0.94

36.64

Diisooctyl phthalate

C24H38O4

1.95

42.85

Ethyl iso-allocholate

C26H44O5

0.87

43.51

1H-2,8a-Methanocyclopenta[a]cycl opropa[e]cyclodecen-11-one, 1a,2,5,5a,6,9,10,10a-octahydro-5,5a,6-trihydroxy-1,4-bis(hydroxymethy l)-1,7,9-trimethyl-, [1S-(1à,1aà,2à,5á,5aá,6á,8aà,9à,10 aà)]-

C20H28O6

1.52

43.75

Stigmast-5-en-3-ol, (3á,24S)-

C29H50O

1.07

44.78

Ethyl iso-allocholate

C26H44O5

2.71

45.89

Ethyl iso-allocholate

C26H44O5

0.79

47.15

Rhodopin

C40H58O

1.11

47.44

Rhodopin

C40H58O

0.54

48.61

Rhodopin

C40H58O

1.50