16-hydroxyandrost-4-en-3,17-dione has been researched along with estriol in 7 studies
*Estriol: A hydroxylated metabolite of ESTRADIOL or ESTRONE that has a hydroxyl group at C3, 16-alpha, and 17-beta position. Estriol is a major urinary estrogen. During PREGNANCY, a large amount of estriol is produced by the PLACENTA. Isomers with inversion of the hydroxyl group or groups are called epiestriol. [MeSH]
*Estriol: A hydroxylated metabolite of ESTRADIOL or ESTRONE that has a hydroxyl group at C3, 16-alpha, and 17-beta position. Estriol is a major urinary estrogen. During PREGNANCY, a large amount of estriol is produced by the PLACENTA. Isomers with inversion of the hydroxyl group or groups are called epiestriol. [MeSH]
| Studies (16-hydroxyandrost-4-en-3,17-dione) | Trials (16-hydroxyandrost-4-en-3,17-dione) | Recent Studies (post-2010) (16-hydroxyandrost-4-en-3,17-dione) | Studies (estriol) | Trials (estriol) | Recent Studies (post-2010) (estriol) |
|---|---|---|---|---|---|
| 20 | 0 | 1 | 6,243 | 309 | 447 |
| Protein | Taxonomy | 16-hydroxyandrost-4-en-3,17-dione (IC50) | estriol (IC50) |
|---|---|---|---|
| Estrogen receptor | Homo sapiens (human) | 0.0017 | |
| Polyunsaturated fatty acid lipoxygenase ALOX15 | Oryctolagus cuniculus (rabbit) | 8.635 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (57.14) | 18.7374 |
| 1990's | 2 (28.57) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Numazawa, M; Osawa, Y | 1 |
| Furihata, R; Ishikawa, S; Konno, T; Numazawa, M | 1 |
| Oakey, RE; Purohit, A | 1 |
| Numazawa, M; Osada, R; Osawa, Y; Tsuji, M | 1 |
| Biener, A; Bulletti, C; Guller, S; Gurpide, E | 1 |
| Oakey, RE; Othman, YS | 1 |
| Matsuzaki, H; Numazawa, M; Watari, Y; Yoshimura, A | 1 |
7 other study(ies) available for 16-hydroxyandrost-4-en-3,17-dione and estriol
| Article | Year |
|---|---|
Improved synthesis of 16alpha-hydroxylated androgens: intermediates of estriol formation in pregnancy.
Topics: Androgens; Androstenedione; Animals; Dehydroepiandrosterone; Estriol; Female; Hydroxytestosterones; Magnetic Resonance Spectroscopy; Methods; Oxidation-Reduction; Pregnancy; Spectrophotometry, Infrared | 1978 |
Determination of aromatization of 19-oxygenated 16 alpha-hydroxyandrostenedione with human placental microsomes by high-performance liquid chromatography coupled with coulometric detection.
Topics: Androstenedione; Aromatase; Chromatography, High Pressure Liquid; Estriol; Female; Humans; Hydroxyestrones; Kinetics; Microsomes; Placenta; Substrate Specificity | 1990 |
Evidence for separate sites for aromatisation of androstenedione and 16 alpha-hydroxyandrostenedione in human placental microsomes.
Topics: Androstenedione; Aromatase; Aromatase Inhibitors; Estradiol; Estriol; Estrone; Female; Humans; Hydroxyestrones; In Vitro Techniques; Kinetics; Microsomes; Placenta; Pregnancy; Radioimmunoassay | 1989 |
High-performance liquid chromatographic determination of aromatization of 16 alpha-hydroxylated androgens with human placental microsomes.
Topics: Androgens; Androstenedione; Chromatography, Gel; Chromatography, High Pressure Liquid; Estriol; Gas Chromatography-Mass Spectrometry; Humans; Hydroxyestrones; Hydroxytestosterones; In Vitro Techniques; Kinetics; Microchemistry; Microsomes; Placenta | 1985 |
Relative distribution of estrone, estradiol and estriol between fetal and maternal perfusates during perfusions of human term placentas with labelled C19 precursors.
Topics: Androstenedione; Estradiol; Estriol; Estrone; Ethinyl Estradiol; Female; Humans; In Vitro Techniques; Perfusion; Placenta; Pregnancy; Time Factors; Tissue Distribution | 1984 |
Why so much oestriol? A comparison of the aromatisation of androstenedione and 16 alpha-hydroxyandrostenedione when incubated alone or together with human placental microsomes.
Topics: Androstenedione; Aromatase; Estradiol; Estriol; Humans; In Vitro Techniques; Microsomes; Placenta; Radioimmunoassay | 1996 |
Aromatase inhibition by 4 beta,5 beta-epoxides of 16 alpha-hydroxyandrostenedione and its 19-oxygenated analogs, potential precursors of estriol production in the feto-placental unit.
Topics: Androstenedione; Aromatase; Aromatase Inhibitors; Enzyme Inhibitors; Epoxy Compounds; Estriol; Fetus; Humans; Placenta | 2002 |