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  • Flavonoids as opioid receptor ligands: identification and preliminary structure-activity relationships.

Flavonoids as opioid receptor ligands: identification and preliminary structure-activity relationships.

Journal of natural products (2007-08-10)
Peter L Katavic, Kenneth Lamb, Hernan Navarro, Thomas E Prisinzano
ZUSAMMENFASSUNG

Flavonoids have been recognized as the active ingredients of many medicinal plant extracts due to interactions with proteins via phenolic groups and low toxicity. Here, we report the investigation of the flavonoid core as a potential new scaffold for the development of opioid receptor ligands. Biological results suggest that stereochemistry of the C2 and C3 positions is important for antagonist activity and selectivity. Our results also suggest that the actions of Hypericum perforatum may be mediated in part by opioid receptors.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
(−)-Epicatechin, ≥90% (HPLC)
Sigma-Aldrich
Apigenin, ≥95.0% (HPLC)
Sigma-Aldrich
Quercetin-3-β-D-glucosid, ≥90% (HPLC)
Sigma-Aldrich
(−)-Epicatechin, ≥98% (HPLC), from green tea
Sigma-Aldrich
Daidzein, ≥98%, synthetic
Sigma-Aldrich
(−)-Catechin-Gallat, ≥98% (HPLC), from green tea
Sigma-Aldrich
(−)-Catechin, ≥97% (HPLC), from green tea
Sigma-Aldrich
Amentoflavon, ≥98.0% (HPLC)
Sigma-Aldrich
(−)-Epicatechin-Gallat, ≥98% (HPLC), from green tea
Sigma-Aldrich
(−)-Epigallocatechin, ≥95% (HPLC), from green tea
Isoquercitrin, primary reference standard
Supelco
(−)-Epicatechin, analytical standard
Supelco
(−)-Epigallocatechin, analytical standard
Supelco
Quercetin-3-glucosid, analytical standard