Cultured roots of Xiphidium caeruleum: Phenylphenalenones and their biosynthetic and extractant-dependent conversion.

@article{Chen2017CulturedRO,
  title={Cultured roots of Xiphidium caeruleum: Phenylphenalenones and their biosynthetic and extractant-dependent conversion.},
  author={Yu Chen and Christian Paetz and Riya C. Menezes and Bernd Schneider},
  journal={Phytochemistry},
  year={2017},
  volume={133},
  pages={
          15-25
        }
}
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References

SHOWING 1-10 OF 27 REFERENCES

Organ-specific analysis of phenylphenalenone-related compounds in Xiphidium caeruleum.

HPLC–NMR for tissue‐specific analysis of phenylphenalenone‐related compounds in Xiphidium caeruleum (Haemodoraceae)

HPLC–1H NMR has been used to study the tissue‐specific distribution of phenylphenalenones, polyphenolic natural products of Xiphidium caeruleum, a neotropical member of the Haemodoraceae plant

Phenylphenalenone-related compounds: chemotaxonomic markers of the haemodoraceae from Xiphidium caeruleum.

Phytochemical analysis of Xiphidium caeruleum resulted in the isolation and identification of a variety of phenylphenalenone-related compounds, which are used as the basis to elaborate biogeographic characteristics of this plant family.

Histochemical analysis of phenylphenalenone-related compounds in Xiphidium caeruleum (Haemodoraceae)

The present results provide new insights into the possible functions of phenylphenalenone-related compounds in the context of their localisation and the advantages and limitations of the techniques are discussed.