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. 2022 Feb 14;11(2):385. doi: 10.3390/antiox11020385

Table 6.

The antioxidant activities of isolated components from Anemarrhena asphodeloides determined with DPPH, ABTS, superoxide radical scavenging, and ferric-reducing antioxidant power (FRAP) assays.

Compounds DPPH
IC50 (μg/mL)
ABTS
IC50 (μg/mL)
Superoxide
IC50 (μg/mL)
FRAP (mM/g) c
(TE)
Mangiferin 5.4 ± 0.3 * 3.7 ± 0.2 * 53.8 ± 2.4 * 9371.4 ± 183.9 ***
Timosaponin A-III >200 >200 >200 19.5 ± 3.9 *
Neomangiferin >200 81.9 ± 4.6 ** >200 83.1 ± 5.3 **
Isomangiferin 16.7 ± 1.1 * 5.6 ± 0.4 * 155.3 ± 13.8 * 6359.9 ± 176.8 ***
BHT a 27.2 ± 1.9 * 15.4 ± 0.9 * N.A. b 3963.9 ± 104.0 ***

Results are expressed as half inhibitory concentration (IC50) of each free-radical scavenging activity. a Butylated hydroxytoluene (BHT) used as positive control. b N.A. indicates not available (poor solubility). c Ferric-reducing antioxidant power (FRAP) assay expressed as millimolar (mM) of Trolox equivalents (TE) per gram of extract. * p < 0.05, ** p < 0.01, and *** p < 0.001 compared with the control.