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Research Article

Secondary metabolites of Hypericum scabrum and Hypericum bupleuroides

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Pages 847-853 | Received 29 Mar 2008, Accepted 27 Jun 2008, Published online: 02 Jul 2009

Figures & data

Figure 1. Typical chromatogram of H. bupleuroides flower extract obtained by HPLC separation at 270 nm. Peak identified: 1 –hyperforin.

Figure 1.  Typical chromatogram of H. bupleuroides flower extract obtained by HPLC separation at 270 nm. Peak identified: 1 –hyperforin.

Figure 2. Typical chromatograms of Hypericum scabrum (A) and H. bupleuroides (B) flower extracts obtained by HPLC separation at 590 nm. Peak identified: 1–pseudohypericin, 2–hypericin.

Figure 2.  Typical chromatograms of Hypericum scabrum (A) and H. bupleuroides (B) flower extracts obtained by HPLC separation at 590 nm. Peak identified: 1–pseudohypericin, 2–hypericin.

Figure 3. Typical chromatograms of Hypericum scabrum (A) and H. bupleuroides (B) flower extracts obtained by HPLC separation at 360 nm. Peak identified: 1–chlorogenic acid, 2–rutin, 3–hyperoside, 4–apigenin-7-O-glucoside, 5–quercitrin, 6–quercetin, 7–kaempferol, 8–amentoflavone.

Figure 3.  Typical chromatograms of Hypericum scabrum (A) and H. bupleuroides (B) flower extracts obtained by HPLC separation at 360 nm. Peak identified: 1–chlorogenic acid, 2–rutin, 3–hyperoside, 4–apigenin-7-O-glucoside, 5–quercitrin, 6–quercetin, 7–kaempferol, 8–amentoflavone.

Table 1. Secondary metabolite concentrations in stem, leaf and flower of Hypericum scabrum and H. bupleuroides (mg/g DW). Data are means of three extracts prepared from a pooled sample of 30 plants for each species.

Table 2. Comparison of the contents of secondary metabolites (mg/g DW) in H. scabrum, H. bupleuroides (this study) and H. perforatum (compiled from various sources).

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