Identification of novel indole based heterocycles as selective estrogen receptor modulator.

Bioorganic Chemistry(2018)

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摘要
•Indole heterocycles were rationally designed and synthesised as SERM.•Compounds 5c and 6d reduced the mRNA and protein expression of ER-α.•Compound were able to accumulate in nucleoplasm, cytoplasm and biomembrane.•Alkyl substitution is well tolerated than aryl substitution.
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关键词
Breast cancer,Chromene,Estrogen receptor,Indole derivatives,Dihydropyridine
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