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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
摘要

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.

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Sigma-Aldrich
(−)-表儿茶素, ≥90% (HPLC)
Sigma-Aldrich
芹菜素, ≥95.0% (HPLC)
Sigma-Aldrich
槲皮素 3-β-D-葡萄糖甙, ≥90% (HPLC)
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(−)-表儿茶素, ≥98% (HPLC), from green tea
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黄豆苷元, ≥98%, synthetic
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(−)-儿茶素没食子酯酸, ≥98% (HPLC), from green tea
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(-)-儿茶素, ≥97% (HPLC), from green tea
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Amentoflavone, ≥98.0% (HPLC)
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(−)-表儿茶素没食子酸酯, ≥98% (HPLC), from green tea
Sigma-Aldrich
(-)-表没食子儿茶素, ≥95% (HPLC), from green tea
Supelco
(−)-表儿茶素, analytical standard
异栎素, primary reference standard
Supelco
槲皮素 3-葡萄糖苷, analytical standard
Supelco
(-)-表没食子儿茶素, analytical standard