The discovery of new and more potent chloropyramine (C4) analogues for the potential treatment of invasive breast cancer-Reference-Cited by-同舟云学术

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The discovery of new and more potent chloropyramine (C4) analogues for the potential treatment of invasive breast cancer

Published:2017-08-30 Issue:1 Volume:91 Page:314-321
ISSN:1747-0277
Container-title:Chemical Biology & Drug Design
language:en
Short-container-title:Chem Biol Drug Des

Author:

Kandil Sahar¹^ORCID,Prencipe Filippo¹,Jones Samuel¹,Hiscox Stephen¹,Westwell Andrew D.¹^ORCID

Affiliation:

1. School of Pharmacy & Pharmaceutical Sciences; Cardiff University; Cardiff Wales UK

Funder

Life Sciences Research Network Wales

Publisher

Wiley

Subject

Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cbdd.13083/fullpdf

Reference20 articles.

1. Src and focal adhesion kinase as therapeutic targets in cancer

2. Knockdown of focal adhesion kinase reverses colon carcinoma multicellular resistance

3. Disrupting the Scaffold to Improve Focal Adhesion Kinase–Targeted Cancer Therapeutics

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3. Discovery of novel chloropyramine-cinnamic acid hybrids as potential FAK inhibitors for intervention of metastatic triple-negative breast cancer;Bioorganic & Medicinal Chemistry;2022-07

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5. Structure-Based Virtual Screening, Synthesis and Biological Evaluation of Potential FAK-FAT Domain Inhibitors for Treatment of Metastatic Cancer;Molecules;2020-07-31

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