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  • Discovery of estrogen receptor α modulators from natural compounds in Si-Wu-Tang series decoctions using estrogen-responsive MCF-7 breast cancer cells.

Discovery of estrogen receptor α modulators from natural compounds in Si-Wu-Tang series decoctions using estrogen-responsive MCF-7 breast cancer cells.

Bioorganic & medicinal chemistry letters (2011-12-06)
Li Liu, Hongyue Ma, Yuping Tang, Wenxing Chen, Yin Lu, Jianming Guo, Jin-Ao Duan
ABSTRACT

The binding between the estrogen receptor α (ER-α) and a variety of compounds in traditional Chinese formulae, Si-Wu-Tang (SWT) series decoctions, was studied using a stably-transfected human breast cancer cell line (MVLN). In 38 compounds tested from SWT series decoctions, the estrogen-like activity of 22 compounds was above 60% in 20 μg mL(-1). Furthermore, theoretical affinity of these compounds was certificated using the functional virtual screen of ER-α modulators by FlexX-Pharm. The accuracy of functional virtual screening of ER-α modulators could reach to 77.27%. The results showed that some compounds, such as organic acids and flavones in SWT series decoctions could be used as selective estrogen receptor modulators (SERMs) and could be selected for further development as potential agents for estrogen related diseases.

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Acido linoleico, ≥99%
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p-Anisaldehyde, 98%
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p-Coumaric acid, ≥98.0% (HPLC)
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Acido linoleico, liquid, BioReagent, suitable for cell culture
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Benzaldehyde, purified by redistillation, ≥99.5%
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Zimtaldehyd, natural, ≥95%, FG
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Kaempferol, ≥97.0% (HPLC)
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trans-Ferulic acid, 99%
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trans-Cinnamaldehyde, 97%
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Benzaldehyde, ReagentPlus®, ≥99%
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trans-Cinnamic acid, ≥99%
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3,4-Dihydroxybenzoic acid, ≥97.0% (T)
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Berberine chloride form
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Kaempferol, ≥90% (HPLC), powder
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Vanillic acid, 97%
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Baicalein, 98%
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trans-Cinnamaldehyde, ≥99%
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trans-Cinnamic acid, 97%
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trans-Ferulic acid, ≥99%
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trans-Cinnamic acid, ≥99%, FG
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