Hydroxylated triphenylacrylonitriles adopt a unique orientation within the binding site of the estrogen receptor
- 1 August 1990
- journal article
- research article
- Published by Elsevier in Journal of Steroid Biochemistry
- Vol. 36 (5) , 391-397
- https://doi.org/10.1016/0022-4731(90)90079-8
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growthJournal of Medicinal Chemistry, 1989
- Analogies and differences in the modulation of progesterone receptor induction and cell proliferation by estrogens and antiestrogens in MCF-7 human breast cancer cells: Study with 24 triphenylacrylonitrile derivativesThe Journal of Steroid Biochemistry and Molecular Biology, 1988
- Ligand Interaction at the Estrogen Receptor to Program Antiestrogen Action: A Study With Nonsteroidal Compoundsin Vitro*Endocrinology, 1988
- Mechanism of the Estrogen Receptor Interaction with 4-HydroxytamoxifenMolecular Endocrinology, 1988
- Comparison of the Physicochemical Properties of Uterine Nuclear Estrogen Receptors Bound to Estradiol or 4-Hydroxytamoxifen*Endocrinology, 1986
- Hydroxy derivatives of tamoxifenJournal of Medicinal Chemistry, 1985
- Influence of new hydroxylated Triphenylethylene (TPE) derivatives on estradiol binding to uterine cytosolJournal of Steroid Biochemistry, 1984
- Inhibition of prostaglandin synthetase by di- and triphenylethylene derivatives: a structure-activity studyJournal of Medicinal Chemistry, 1983
- Geometric Isomers of Substituted Triphenylethylenes and Antiestrogen ActionEndocrinology, 1981
- Script: interactive molecular geometrical treatments on the basis of computer-drawn chemical formulaTetrahedron, 1981