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. 2016 Sep 16;21(9):1241. doi: 10.3390/molecules21091241

Table 3.

Inhibitory effect of isolated compounds from X. strumarium on α-glucosidase.

Entry Products Concentration (μg/mL) Inhibition (%) IC50 1 (μg/mL)
Acarbose 2 1000 106.14 377.19 ± 37.8 (584.79 μM)
500 60.29
250 41.06
50 16.98
1 Protocatechuic acid 50 17.45 -
2 3-Hydroxy-1-(4-hydroxy phenyl) propan-1-one 50 8.60 -
3 Cytidine 50 4.70 -
4 Neochlorogenic acid methyl ester 50 - -
5 Chlorogenic acid 50 6.60 -
6 Methyl-3,5-di-O-caffeoylquinic acid 25 96.50 9.78 ± 0.79 (18.42 μM)
12.5 59.11
5 40.00
2.5 22.63
7 Thiazine-3,5-dione-11-O-glucopyranoside 50 10.18 -
8 Patuletin-3-glucuronide 50 6.11 -
9 Quercetin-3-O-glucuronide 50 15.40 -
10 3,5-di-O-caffeoylquinic acid 100 99.44 45.48 ± 4.52 (88.14 μM)
50 52.85
25 33.72
5 9.34
11 1,5-di-O-caffeoylquinic acid 50 46.20 -
12 1,3-di-O-caffeoylquinic acid 50 38.37 -
13 1,3,5-tri-O-caffeoylquinic acid 50 22.05 -
14 Raffinose 50 5.82 -

1 The IC50 value was defined as the half-maximal inhibitory concentration and mean of 3 duplication analyses of each sample. 2 Acarbose was used as the positive control. - is no activity.

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