Facile geometric isomerization of phenolic non-steroidal estrogens and antiestrogens: limitations to the interpretation of experiments characterizing the activity of individual isomers.
Katzenellenbogen, J A
Facile geometric isomerization of phenolic non-steroidal estrogens and antiestrogens: limitations to the interpretation of experiments characterizing the activity of individual isomers. [electronic resource] - Journal of steroid biochemistry May 1985 - 589-96 p. digital
Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
0022-4731
10.1016/0022-4731(85)90210-9 doi
Animals
Antioxidants--pharmacology
Breast Neoplasms--metabolism
Cells, Cultured
Chromatography, High Pressure Liquid
Diethylstilbestrol--metabolism
Female
Humans
Phenols--metabolism
Rats
Receptors, Estrogen--metabolism
Stereoisomerism
Tamoxifen--analogs & derivatives
Uterus--metabolism
Facile geometric isomerization of phenolic non-steroidal estrogens and antiestrogens: limitations to the interpretation of experiments characterizing the activity of individual isomers. [electronic resource] - Journal of steroid biochemistry May 1985 - 589-96 p. digital
Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
0022-4731
10.1016/0022-4731(85)90210-9 doi
Animals
Antioxidants--pharmacology
Breast Neoplasms--metabolism
Cells, Cultured
Chromatography, High Pressure Liquid
Diethylstilbestrol--metabolism
Female
Humans
Phenols--metabolism
Rats
Receptors, Estrogen--metabolism
Stereoisomerism
Tamoxifen--analogs & derivatives
Uterus--metabolism