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Novel 3-Aryl Indoles as Progesterone Receptor Antagonists for Uterine Fibroids
[Image: see text] We report the synthesis and characterization of novel 3-aryl indoles as potent and efficacious progesterone receptor (PR) antagonists with potential for the treatment of uterine fibroids. These compounds demonstrated excellent selectivity over other steroid nuclear hormone receptor...
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| Główni autorzy: | , , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
American Chemical Society
2010
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| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4017981/ https://ncbi.nlm.nih.gov/pubmed/24900294 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ml100220b |
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