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. 2014 Nov 3;19(11):17829–17838. doi: 10.3390/molecules191117829

Table 1.

Antioxidant activity of the extracted compounds at 100 μM.

Compounds ABTS (%) DPPH (%) Chelating (%) Reducing Power (OD 700)
Liriodenine (1) 12.9 na 3.4 0.105
Lysicamine (2) 6.4 24.7 7.8 0.302
(−)-Anonaine (3) 14.2 na 1.7 0.128
(−)-Asimilobine (4) 12.4 3.9 5.2 0.109
(−)-Caaverine (5) na na 7.8 0.225
(−)-N-Methylasimilobine (6) 23.5 na 6.9 0.116
(−)-Nuciferine (7) 2.8 9.1 11.3 0.110
(−)-Nornuciferine (8) 5.6 16.9 7.8 0.075
(−)-Roemerine (9) 1.8 na 1.7 0.090
7-Hydroxydehydronuciferine (10) 5.3 na na 0.120
Cepharadione B (11) 3.2 5.0 7.5 0.135
β-Sitostenone (12) na 1.3 na -
Phenophytin-A (14) 6.8 1.2 10.4 -
Aristophyll-C (15) na 1.3 6.9 -
MeOH extract 35.6 40.2 13.3 -
Vitamin C 97 100 - -
EDTA - - 26.8 -
BHA - - - 0.603

Data in the table are means ± S.D. of n = 3; -: no testing; na: not active.

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