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. 2021 Oct 20;26(21):6331. doi: 10.3390/molecules26216331

Table 1.

Antioxidant activity of fifteen triterpenes, employing the phosphomolybdenum method, and metal-chelating activity on ferrous ion assays.

Compounds Phosphomolybenum
(mmol TE/g)
Metal-Chelating
(mg EDTAE/g)
Cycloorbicoside A (1) 1.82 ± 0.04 18.54 ± 0.06
Cycloorbicoside A-7-monoacetate (2) 2.26 ± 0.22 41.00 ± 0.37
3-O-β-d-Xylopyranoside-(23R,24S)-16β,23;16α,24-diepoxycycloart-25(26)-en-3β,7β-diol 2′,3′,4′,7-tetraacetate (3) 1.98 ± 0.06 18.16 ± 0.72
3-O-β-d-Xylopyranoside-(23R,24S)-16β,23;16α,24-diepoxycycloart-25(26)-en-3β,7β-diol-7-monoacetate (4) 1.34 ± 0.01 21.88 ± 0.96
3-O-β-d-Xylopyranoside-(23R,24S)-16β,23;16α,24-diepoxycycloart-25(26)-en-3β,7β-diol (5) 0.80 ± 0.01 15.64 ± 0.28
Cycloalpioside D (6) 4.05 ± 0.01 19.03 ± 0.07
Cycloalpioside D-2′,3′,4′,7-tetraacetate (7) 1.58 ± 0.16 25.38 ± 0.08
Cycloalpioside D-2′,3′,4′-triacetate (8) 1.78 ± 0.02 19.26 ± 0.33
3-O-β-d-Xylopyranoside-20R-25-norcycloartan-3β,7β,16β-triol-20,24-olide (9) 0.45 ± 0.02 20.19 ± 0.21
Cycloorbicoside B (10) 1.49 ± 0.17 4.68 ± 0.08
Cyclosieversioside E (11) 1.90 ± 0.16 8.33 ± 0.24
Astragaloside IV (12) 1.30 ± 0.04 8.73 ± 0.04
Cyclosieversioside H (13) 0.83 ± 0.06 3.96 ± 0.14
Oleanolic acid (14) 0.20 ± 0.01 3.05 ± 0.14
Ursolic acid (15) 0.42 ± 0.10 30.17 ± 0.07

Values are reported as mean ± S.D.; TE: Trolox equivalents; and EDTAE: EDTA equivalents.