alkenes has been researched along with 1-(4-hydroxyphenyl)-1,2-diphenyl-1-butene in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 4 (80.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bodell, WJ; Burlingame, AL; Nakamura, T; Pathak, DN; Pongracz, K | 1 |
Lee, HK; Li, SF; Ng, CL; Ong, CP | 1 |
Bodell, WJ; Pathak, DN; Pongracz, K | 1 |
Barakat, RR | 1 |
Brauch, H; Eichelbaum, M; Johänning, J; Kröner, P; Mürdter, TE; Nörenberg, A; Schroth, W; Schwab, M; Thomas, M; Zanger, UM | 1 |
1 review(s) available for alkenes and 1-(4-hydroxyphenyl)-1,2-diphenyl-1-butene
Article | Year |
---|---|
Tamoxifen and the endometrium.
Topics: Alkenes; Animals; Antineoplastic Agents, Hormonal; Breast Neoplasms; Carcinoma; Clinical Trials as Topic; Endometrial Neoplasms; Endometrium; Estrogen Antagonists; Estrogens; Female; Genes, ras; Humans; Hyperplasia; Leiomyosarcoma; Mass Screening; Menopause; Mice; Mice, Nude; Neoplasm Transplantation; Neoplasms, Hormone-Dependent; Neoplasms, Second Primary; Phenols; Polyps; Receptors, Estrogen; Risk; Tamoxifen | 1998 |
4 other study(ies) available for alkenes and 1-(4-hydroxyphenyl)-1,2-diphenyl-1-butene
Article | Year |
---|---|
Activation of the tamoxifen derivative metabolite E to form DNA adducts: comparison with the adducts formed by microsomal activation of tamoxifen.
Topics: Alkenes; Animals; Benzene Derivatives; Biotransformation; DNA; DNA Adducts; Female; Horseradish Peroxidase; Microsomes, Liver; NADP; Oxidation-Reduction; Phenols; Rats; Tamoxifen | 1995 |
Determination of pharmaceuticals and related impurities by capillary electrophoresis.
Topics: 2-Hydroxypropyl-beta-cyclodextrin; Alkenes; beta-Cyclodextrins; Capillary Action; Chromatography, High Pressure Liquid; Cyclodextrins; Drug Contamination; Electrophoresis; gamma-Cyclodextrins; Hydrogen-Ion Concentration; Micelles; Ondansetron; Phenols; Reproducibility of Results; Sensitivity and Specificity; Tamoxifen; Technology, Pharmaceutical | 1994 |
Activation of 4-hydroxytamoxifen and the tamoxifen derivative metabolite E by uterine peroxidase to form DNA adducts: comparison with DNA adducts formed in the uterus of Sprague-Dawley rats treated with tamoxifen.
Topics: Alkenes; Animals; Biotransformation; DNA Adducts; Female; Horseradish Peroxidase; Liver; Molecular Structure; Peroxidases; Phenols; Rats; Rats, Sprague-Dawley; Tamoxifen; Uterus | 1996 |
The formation of estrogen-like tamoxifen metabolites and their influence on enzyme activity and gene expression of ADME genes.
Topics: Alkenes; Cell Line; Cytochrome P-450 Enzyme System; Estrogens; Gene Expression Regulation, Enzymologic; Glucuronides; Glucuronosyltransferase; Hepatocytes; Humans; Microsomes, Liver; Phenols; Tamoxifen | 2018 |