Synthesis of 16α-[125I]iodo-5α-dihydrotestosterone and evaluation of its affinity for the androgen receptor
- 30 April 1982
- journal article
- research article
- Published by Elsevier in The Journal of Steroid Biochemistry and Molecular Biology
- Vol. 16 (5) , 621-628
- https://doi.org/10.1016/0022-4731(82)90097-8
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Biological activity of [127I] and [125I] estradiol analogs in vitro and in vivoJournal of Steroid Biochemistry, 1981
- The uptake of radioiodinated 5?-dihydrotestosterone by the prostate of intact and castrated ratsEuropean Journal of Nuclear Medicine and Molecular Imaging, 1981
- Iododerivatives of testosterone as potential biological markersThe Journal of Steroid Biochemistry and Molecular Biology, 1980
- The synthesis of 77Br-labelled 5α-dihydrotestosterone and a comparison of its distribution in rats with 77Br-bromideThe International Journal of Applied Radiation and Isotopes, 1979
- Iodine-125—Labeled Estradiol: a Gamma-Emitting Analog of Estradiol That Binds to the Estrogen ReceptorScience, 1979
- Androgen Receptor Assay with [3H]Methyltrienolone (R1881) in the Presence of Progesterone Receptors*Endocrinology, 1979
- Saline hydrides and superbases in organic reactions. II. Facile reaction of potassium hydride with ketones. Rapid, quantitative formation of potassium enolates from ketones via kaliationThe Journal of Organic Chemistry, 1974
- Gem-dialkyl effect. III. Kinetic and equilibrium studies of steroid cyclic ketal formation and hydrolysisJournal of the American Chemical Society, 1968
- Gem-dialkyl effect. II. Comparison of the kinetic and equilibrium approaches to the sective ketalization of 5.alpha.-androstane-3,17-dione with various glycolsJournal of the American Chemical Society, 1968
- 619. Steroids and walden inversion. Part XL. The configurations of the bromination products of androstan-17-oneJournal of the Chemical Society, 1958