1624-62-0
1624-62-0
Chemical Structure
Estrone 3-methyl ether
Synonym(s): Oestrone methyl ether; 3-O-Methylestrone
- CAS No.: 1624-62-0
- Formula:C19H24O2
- Molecular Weight:284.39
IUPAC Name: (8R,9S,13S,14S)-3-methoxy-13-methyl-7,8,9,11,12,13,15,16-octahydro-6H-cyclopenta[a]phenanthren-17(14H)-one
InChIKey: BCWWDWHFBMPLFQ-VXNCWWDNSA-N
SMILES: C[C@@]12[C@](CCC2=O)([H])[C@@]3([H])[C@@](CC1)([H])C4=CC=C(OC)C=C4CC3
Biological Activity: Estrone 3-methyl ether (Oestrone methyl ether; 3-O-Methylestrone) is a synthetic intermediate useful for synthesis of estrogen receptor modulator[1][2][3].
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Estrone 3-methyl ether | 97.38% | Estrone 3-methyl ether (Oestrone methyl ether; 3-O-Methylestrone) is a synthetic intermediate useful for synthesis of estrogen receptor modulator. | ||||||||||||||||||||
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Estrone 3-methyl ether-13C6 | Estrone 3-methyl ether-13C6 is a 13C-labeled Estrone 3-methyl ether (HY-79576). Estrone 3-methyl ether (Oestrone methyl ether; 3-O-Methylestrone) is a synthetic intermediate useful for synthesis of estrogen receptor modulator. | |||||||||||||||||||||
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Estrone 3-methyl ether-d3 | Estrone 3-methyl ether-d3 is the deuterium labeled Estrone 3-methyl ether. | |||||||||||||||||||||
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References
- [1]. Kuznetsov YV, et al. New estrogen receptor antagonists. 3,20-Dihydroxy-19-norpregna-1,3,5(10)-trienes: Synthesis, molecular modeling, and biological evaluation. Eur J Med Chem. 2018 Jan 1;143:670-682. [Content Brief]
- [2]. Herman BE, et al. Comparative investigation of the in vitro inhibitory potencies of 13-epimeric estrones and D-secoestrones towards 17β-hydroxysteroid dehydrogenase type 1. J Enzyme Inhib Med Chem. 2016;31(sup3):61-69. [Content Brief]
