Table 4.
Treatment | Inhibition (%) | ||||
---|---|---|---|---|---|
0 µM | 1 µM | 3 µM | 10 µM | 30 µM | |
Gedunin (1) | 0.0 ± 2.1 | 4.5 ± 1.9 | 21.8 ± 3.7 ** | 38.1 ± 3.8 ** | 36.5 ± 4.1 ** |
6α-Acetoxygedunin (2) | 0.0 ± 1.6 | 10.9 ± 1.0 ** | 23.2 ± 1.8 ** | 36.3 ± 2.1 ** | 37.3 ± 1.4 ** |
7-Deacetoxy-7-oxogedunin (3) | 0.0 ± 1.1 | 5.8 ± 1.5 | 26.7 ± 4.5 ** | 58.6 ± 7.2 ** | 68.7 ± 4.8 ** |
7-Deacetoxy-7α-hydroxygedunin (4) | 0.0 ± 0.3 | −6.5 ± 2.4 | 2.7 ± 2.3 | 36.5 ± 1.8 ** | |
Andirolide H (5) | 0.0 ± 0.8 | −6.6 ± 3.6 | −0.7 ± 1.2 | 7.6 ± 1.1 | 39.2 ± 1.7 ** |
6α-Hydroxygedunin (6) | 0.0 ± 1.3 | 8.1 ± 1.9 | 6.7 ± 1.5 | 12.1 ± 3.0 | 28.3 ± 1.7 ** |
Methyl angolensate (7) | 0.0 ± 1.4 | −0.5 ± 3.5 | 0.6 ± 2.9 | 13.3 ± 2.6 * | 24.6 ± 2.9 ** |
Epoxyazadiradione (8) | 0.0 ± 5.3 | 13.7 ± 3.9 | 39.1 ± 6.5 ** | 91.5 ± 11.4 ** | |
17β-Hydroxyazadiradione (9) | 0.0 ± 1.5 | 14.1 ± 3.4 | 23.9 ± 3.9 ** | 64.0 ± 3.3 ** | 91.3 ± 8.2 ** |
Carapanolide C (10) | 0.0 ± 3.7 | 4.9 ± 2.1 | 14.2 ± 3.2 | 27.7 ± 4.3 ** | 54.5 ± 5.5 ** |
Carapanolide R (11) | 0.0 ± 4.1 | −6.3 ± 4.7 | −1.3 ± 3.8 | 31.7 ± 3.8 ** | |
Carapanolide S (12) | 0.0 ± 1.5 | −5.5 ± 2.2 | −1.4 ± 1.5 | −2.5 ± 1.2 | |
Carapanolide M (13) | 0.0 ± 6.5 | −1.5 ± 7.1 | 7.0 ± 4.4 | −5.1 ± 6.2 | |
Carapanolide Q (14) | 0.0 ± 5.5 | 8.6 ± 4.4 | 1.3 ± 4.2 | 9.2 ± 2.5 | |
Carapanolide O (15) | 0.0 ± 6.5 | 6.3 ± 4.3 | 1.0 ± 6.4 | 1.5 ± 4.1 | |
Guianolide A (16) | 0.0 ± 2.9 | −6.2 ± 5.2 | −4.5 ± 1.9 | −7.3 ± 3.0 | |
Carapanolide A (17) | 0.0 ± 3.7 | 8.8 ± 6.5 | 21.5 ± 5.5 ** | 58.2 ± 4.7 ** | |
Treatment | Inhibition (%) | ||||
0 µM | 3 µM | 10 µM | 30 µM | 100 µM | |
Silybin [36] | 0.0 ± 2.6 | 5.3 ± 2.8 | 22.0 ± 3.8 ** | 48.0 ± 4.1 ** | 50.8 ± 3.9 ** |
Each value represents the mean ± S.E.M. (n = 4); asterisks denote significant differences from the control group, * p < 0.05, ** p < 0.01.; commercial silybin was purchased from Funakoshi Co., Ltd. (Tokyo, Japan).