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D-homoestrone methyl ether

Known as: D-Homoestra-1,3,5(10)-trien-17a-one, 3-methoxy- 
 
National Institutes of Health

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2 relations

Broader (1)

Estrone
analogs & derivatives

Papers overview

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2012
2012
Antiproliferative effect of normal and 13-epi-d-homoestrone and their 3-methyl ethers on human reproductive cancer cell lines
The possibility of the therapeutic use of estrogens emerged following the recognition that certain estradiol analogs, and… Expand
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2005
2005
Synthesis von (±)-B-Homoöstron
(±)-B-Homoestrone and its derivatives, a hitherto unknown class of compounds, were synthetized from 3-methoxybenzosuberone as the… Expand
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2003
2003
Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers
An effective epimerization of the normal estrone 3-methyl and 3-benzyl ethers by using o-phenylenediamine and AcOH made the… Expand
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1983
1983
Cytochrome P-450-dependent oxidation of the 17 alpha-ethynyl group of synthetic steroids. D-homoannulation or enzyme inactivation.
Metabolism of the 17 alpha-ethynyl group of the synthetic estrogen, 17 alpha-ethynylestradiol, by hepatic microsomes from female… Expand
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1969
1969
[Synthesis of (plus or minus)-B-homoestrone].
 
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