Side‐Chain Effects on the 1‐(Bis‐aryl‐methylidene)‐[3]ferrocenophane Skeleton: Antiproliferative Activity against TNBC Cancer Cells and Comparison with the Acyclic Ferrocifen Series-Reference-Cited by-同舟云学术

Side‐Chain Effects on the 1‐(Bis‐aryl‐methylidene)‐[3]ferrocenophane Skeleton: Antiproliferative Activity against TNBC Cancer Cells and Comparison with the Acyclic Ferrocifen Series

Published:2016-11-25 Issue:2 Volume:2017 Page:454-465
ISSN:1434-1948
Container-title:European Journal of Inorganic Chemistry
language:en
Short-container-title:Eur. J. Inorg. Chem.

Author:

Gormen Meral¹,Pigeon Pascal¹²^ORCID,Wang Yong²,Vessières Anne²,Top Siden²,Martial Franck²,Gros Christina¹,McGlinchey Michael J.³,Jaouen Gérard¹²

Affiliation:

1. PSL Chimie ParisTech 11 rue Pierre et Marie Curie 75005 Paris France

2. Sorbonne Universités UPMC Univ Paris 06 UMR 8232 IPCM CNRS 75005 Paris France

3. UCD School of Chemistry and Chemical Biology University College Dublin Belfield Dublin 4 Ireland

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejic.201601088

Reference34 articles.

1. European‐Cancer‐Observatory http://eu‐cancer.iarc.fr.

2. Antiestrogens and Selective Estrogen Receptor Modulators as Multifunctional Medicines. 1. Receptor Interactions

3. Synthesis, Biochemical Properties and Molecular Modelling Studies of Organometallic Specific Estrogen Receptor Modulators (SERMs), the Ferrocifens and Hydroxyferrocifens: Evidence for an Antiproliferative Effect of Hydroxyferrocifens on both Hormone-Dependent and Hormone-Independent Breast Cancer Cell Lines

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