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dihydrotestosterone 17-bromoacetate and mercaptoethanol

dihydrotestosterone 17-bromoacetate has been researched along with mercaptoethanol in 1 studies

*Mercaptoethanol: A water-soluble thiol derived from hydrogen sulfide and ethanol. It is used as a reducing agent for disulfide bonds and to protect sulfhydryl groups from oxidation. [MeSH]

*Mercaptoethanol: A water-soluble thiol derived from hydrogen sulfide and ethanol. It is used as a reducing agent for disulfide bonds and to protect sulfhydryl groups from oxidation. [MeSH]

Compound Research Comparison

Studies
(dihydrotestosterone 17-bromoacetate)
Trials
(dihydrotestosterone 17-bromoacetate)
Recent Studies (post-2010)
(dihydrotestosterone 17-bromoacetate)
Studies
(mercaptoethanol)
Trials
(mercaptoethanol)
Recent Studies (post-2010) (mercaptoethanol)
13006,13729279

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Penning, TM; Ricigliano, JW1

Other Studies

1 other study(ies) available for dihydrotestosterone 17-bromoacetate and mercaptoethanol

ArticleYear
Evidence that enzyme-generated aromatic Michael acceptors covalently modify the nucleotide-binding site of 3 alpha-hydroxysteroid dehydrogenase.
    The Biochemical journal, 1990, Aug-01, Volume: 269, Issue:3

    Topics: 3-alpha-Hydroxysteroid Dehydrogenase (B-Specific); 3-Hydroxysteroid Dehydrogenases; Animals; Binding Sites; Chemical Phenomena; Chemistry; Chromatography, Affinity; Dihydrotestosterone; Kinetics; Male; Mercaptoethanol; NAD; NADP; Nitrobenzenes; Nucleotides; Oxidation-Reduction; Protein Synthesis Inhibitors; Rats; Rats, Inbred Strains; Triazines

1990