Page last updated: 2024-08-26

brexanolone and 3-hydroxy-5-androstane-17-carbonitrile

brexanolone has been researched along with 3-hydroxy-5-androstane-17-carbonitrile in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Blinn, JR; Morrow, AL; Paul, SM; Purdy, RH1
Covey, DF; Han, M; Zorumski, CF1
Benz, A; Covey, DF; DeKoster, GT; Evers, AS; Manion, BD; Mennerick, S; Rath, NP; Scaglione, JB; Taylor, A; Zorumski, CF1

Other Studies

3 other study(ies) available for brexanolone and 3-hydroxy-5-androstane-17-carbonitrile

ArticleYear
Synthesis, metabolism, and pharmacological activity of 3 alpha-hydroxy steroids which potentiate GABA-receptor-mediated chloride ion uptake in rat cerebral cortical synaptoneurosomes.
    Journal of medicinal chemistry, 1990, Volume: 33, Issue:6

    Topics: Acetates; Animals; Cerebral Cortex; Chlorides; Desoxycorticosterone; Drug Synergism; Isomerism; Male; Molecular Conformation; Muscimol; Pregnanes; Pregnanolone; Rats; Rats, Inbred Strains; Receptors, GABA-A; Structure-Activity Relationship; Synaptosomes

1990
Neurosteroid analogues. 4. The effect of methyl substitution at the C-5 and C-10 positions of neurosteroids on electrophysiological activity at GABAA receptors.
    Journal of medicinal chemistry, 1996, Oct-11, Volume: 39, Issue:21

    Topics: Animals; Cells, Cultured; Electrophysiology; HEPES; Hippocampus; Hydrogen-Ion Concentration; Methylation; Models, Molecular; Pregnanolone; Rats; Receptors, GABA; Tetrodotoxin

1996
Neurosteroid analogues. 11. Alternative ring system scaffolds: gamma-aminobutyric acid receptor modulation and anesthetic actions of benz[f]indenes.
    Journal of medicinal chemistry, 2006, Jul-27, Volume: 49, Issue:15

    Topics: Animals; Binding, Competitive; Brain; GABA Modulators; In Vitro Techniques; Indenes; Larva; Models, Molecular; Oocytes; Polycyclic Compounds; Radioligand Assay; Rats; Receptors, GABA-A; Stereoisomerism; Steroids; Structure-Activity Relationship; Xenopus laevis

2006