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Research Article

Bioassay-guided isolation, identification of compounds from Origanum rotundifolium and investigation of their antiproliferative and antioxidant activities

, , , , , & show all
Pages 1646-1653 | Received 14 Jun 2016, Accepted 21 Mar 2017, Published online: 21 Apr 2017

Figures & data

Table 1. IC50 values and tumour specificity rate for compounds.

Figure 1. Isolated compounds from O. rotundifolium.

Figure 1. Isolated compounds from O. rotundifolium.

Figure 2. DPPH scavenging, ABTS•+ scavenging and reducing power activities of isolated compounds and positive controls. (The same letters on the columns of DPPH and ABTS revealed that the differences are not significant statistically (p > 0.05). The different letters indicated that the differences are significant (p < 0.05).

Figure 2. DPPH• scavenging, ABTS•+ scavenging and reducing power activities of isolated compounds and positive controls. (The same letters on the columns of DPPH and ABTS revealed that the differences are not significant statistically (p > 0.05). The different letters indicated that the differences are significant (p < 0.05).

Figure 3. The antiproliferative activity of compounds on C6, HeLa, HT29 and Vero cell lines. Cell proliferation was measured using a BrdU Cell Elisa Assay Kit. Percent inhibition was reported as mean values ± SEM of three independent assays (p < 0.05). Each experiment was repeated three times for each cell line.

Figure 3. The antiproliferative activity of compounds on C6, HeLa, HT29 and Vero cell lines. Cell proliferation was measured using a BrdU Cell Elisa Assay Kit. Percent inhibition was reported as mean values ± SEM of three independent assays (p < 0.05). Each experiment was repeated three times for each cell line.
Supplemental material

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