Page last updated: 2024-08-23

alkenes and cyclofenil

alkenes has been researched along with cyclofenil in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Ball, H; Schiller, CD; Schneider, MR1
Einer-Jensen, N; Hanngren, A; Ullberg, S1
Baecker, D; Gaggia, F; Gust, R; Kalchschmid, C; Knox, A; Manzl, C; Schuster, D1

Other Studies

3 other study(ies) available for alkenes and cyclofenil

ArticleYear
Catechol estrogens of the 1,1,2-triphenylbut-1-ene type: relationship between structure, estradiol receptor affinity, estrogenic and antiestrogenic properties, and mammary tumor inhibiting activities.
    Journal of medicinal chemistry, 1986, Volume: 29, Issue:8

    Topics: Alkenes; Animals; Cyclofenil; Diethylstilbestrol; Estrogen Antagonists; Estrogens, Catechol; Female; Magnetic Resonance Spectroscopy; Mammary Neoplasms, Experimental; Mice; Neoplasm Transplantation; Receptors, Estradiol; Receptors, Estrogen; Structure-Activity Relationship

1986
Distribution pattern of a non-steroid compound with endocrine actions, 14C-bis(p-hydroxyphenyl)cyclohexylidenemethane (compound F6060) and its diacetate (compound F6066).
    Acta endocrinologica, 1965, Volume: 50, Issue:1

    Topics: Acetates; Adrenal Glands; Alkenes; Animals; Autoradiography; Brain; Connective Tissue; Cyclofenil; Female; Fetus; Gastric Mucosa; Genitalia, Female; Kidney; Liver; Mice; Muscles; Pancreas; Pituitary Gland; Pregnancy; Pregnancy, Animal; Salivary Glands; Spleen

1965
Development of bivalent triarylalkene- and cyclofenil-derived dual estrogen receptor antagonists and downregulators.
    European journal of medicinal chemistry, 2020, Apr-15, Volume: 192

    Topics: Alkenes; Animals; Cell Line, Tumor; Chlorocebus aethiops; COS Cells; Cyclofenil; Dose-Response Relationship, Drug; Down-Regulation; Drug Development; Estrogen Receptor Antagonists; Humans; Molecular Structure; Receptors, Estrogen; Structure-Activity Relationship

2020