DPPH antiradical assayThe EC50 values on the effect of extracts of C.  translation - DPPH antiradical assayThe EC50 values on the effect of extracts of C.  English how to say

DPPH antiradical assayThe EC50 valu

DPPH antiradical assay
The EC50 values on the effect of extracts of C. albidum on
DPPH scavenging activity showed that petroleum ether
(4057.5 ± 809.6 g/kg) had the least antiradical activity
while ethyl ether (414.4 ± 92.0 g/kg) had the highest
activity (fig. 2). Similarly, the EC50 values of myricetin 3-
rhamnoside (TCA-3) and vitamin C (standard control)
were 314.1 + 60.2 and 127.1 ± 8.6 g/kg respectively (fig.
2). The order of scavenging activity is such that myricetin
3- rhamnoside > ethylacetate extract > n-butanol extract >
ethanol extract > petroleum extract.
Fig. 1: Structure of myricetin 3-rhamnoside.
Fig. 2:
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DPPH antiradical assayThe EC50 values on the effect of extracts of C. albidum onDPPH scavenging activity showed that petroleum ether(4057.5 ± 809.6 g/kg) had the least antiradical activitywhile ethyl ether (414.4 ± 92.0 g/kg) had the highestactivity (fig. 2). Similarly, the EC50 values of myricetin 3-rhamnoside (TCA-3) and vitamin C (standard control)were 314.1 + 60.2 and 127.1 ± 8.6 g/kg respectively (fig.2). The order of scavenging activity is such that myricetin3- rhamnoside > ethylacetate extract > n-butanol extract >ethanol extract > petroleum extract.Fig. 1: Structure of myricetin 3-rhamnoside.Fig. 2:
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DPPH assay antiradical
The EC50 values ​​on the effect of extracts of C. albidum on
DPPH scavenging activity Showed that petroleum ether
(4057.5 ± 809.6 g / kg) had the least antiradical activity
while ethyl ether (414.4 ± 92.0 g / kg) had the highest
activity (fig. 2). Similarly, the EC50 values ​​of myricetin 3-
rhamnoside (TCA-3) and vitamin C (standard control)
were 314.1 + 60.2 and 127.1 ± 8.6 g / kg respectively (fig.
2). The order of scavenging activity is such that myricetin
3- rhamnoside> ethylacetate extract> n-butanol extract>
ethanol extract> petroleum extract.
Fig. 1: Structure of myricetin 3-rhamnoside.
Fig. 2:
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