Synthesis and Evaluation of Novel N-Substituted N′-(3-Hydroxy-17-oxoestra-1,3,5(10)-trien-2- and -4-yl)thiourea Derivatives for Binding to the Estrogen Receptor and Cytotoxic Activity on MCF-7 cells-Reference-Cited by-同舟云学术

Synthesis and Evaluation of Novel N-Substituted N′-(3-Hydroxy-17-oxoestra-1,3,5(10)-trien-2- and -4-yl)thiourea Derivatives for Binding to the Estrogen Receptor and Cytotoxic Activity on MCF-7 cells

Published:1984-12 Issue:12 Volume:73 Page:1871-1873
ISSN:0022-3549
Container-title:Journal of Pharmaceutical Sciences
language:en
Short-container-title:Journal of Pharmaceutical Sciences

Author:

Omar A.-Mohsen M.E.,Aboulwafa Omaima M.,Leclercq G.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

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5. Geometric Isomers of Substituted Triphenylethylenes and Antiestrogen Action

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1. The first Pd-catalyzed Buchwald–Hartwig aminations at C-2 or C-4 in the estrone series;Beilstein Journal of Organic Chemistry;2018-05-04

2. 4′,17-Dioxo-5′H-estra-1(10),4-dieno[3,2-b]furan: Synthesis, Binding Affinity to the Estrogen Receptor, Uterotrophic and Antiimplantation Activities;Archiv der Pharmazie;1996

3. Synthesis and biological evaluation of some novel 2-(pyrimidin-4-yl)estradiol derivatives;European Journal of Medicinal Chemistry;1995-01

4. Synthesis and evaluation for uterotrophic and antiimplantation activities of 2-substituted estradiol derivatives;Steroids;1992-04

5. ESTROGENS, ANTIESTROGENS, AND OTHER ESTRANE COMPOUNDS;Antitumor Steriods;1992