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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
ABSTRACT

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.

MATERIALS
Product Number
Brand
Product Description

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