Chemical compound
Pharmaceutical compound ZK-283197 | |
Other names | BAY 86-5310; SH-T04211C; ZK283197 |
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Routes of administration | By mouth[1] |
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Drug class | Estrogen; Selective ERβ agonist |
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Legal status |
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CAS Number | |
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PubChem CID | |
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UNII | |
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Formula | C20H25FO2 |
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Molar mass | 316.416 g·mol−1 |
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3D model (JSmol) | |
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C[C@]12CC[C@]3([C@H]([C@@H]1C[C@H]([C@@H]2F)O)CCC4=C3C=CC(=C4)O)C=C
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InChI=1S/C20H25FO2/c1-3-20-9-8-19(2)16(11-17(23)18(19)21)15(20)6-4-12-10-13(22)5-7-14(12)20/h3,5,7,10,15-18,22-23H,1,4,6,8-9,11H2,2H3/t15-,16-,17+,18-,19-,20+/m0/s1 Key:LXLNOGZWGYFWQV-CFSBILQPSA-N
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ZK-283197 (also known as BAY 86-5310 or SH-T04211C) is a selective and orally active ERβ agonist which was under development by Bayer Healthcare AG for the treatment of vasomotor symptoms.[1][2] It reached phase II clinical trials prior to the discontinuation of its development.[1] Its development was terminated in 2014.[1]
References
- ^ a b c d "ZK 283197". AdisInsight. Springer Nature Switzerland AG.
- ^ US 332204, Pietras RJ, Jung ME, "Methods of using estrogen receptor-beta ligands as radiation mitigators", published 2015-01-15
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ERTooltip Estrogen receptor | Agonists |
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Mixed (SERMsTooltip Selective estrogen receptor modulators) | |
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Antagonists |
- Coregulator-binding modulators: ERX-11
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GPERTooltip G protein-coupled estrogen receptor | Agonists | |
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Antagonists | |
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Unknown | |
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