trans-IV restriction: a new configuration for metal bis-cyclam complexes as potent CXCR4 inhibitors

Author:

Alzahrani Seraj O.1,McRobbie Graeme1,Khan Abid12,D'huys Thomas3,Van Loy Tom3,Walker Ashlie N.4,Renard Isaline15ORCID,Hubin Timothy J.4ORCID,Schols Dominique3,Burke Benjamin P.1,Archibald Stephen J.15ORCID

Affiliation:

1. Centre for Biomedicine and Positron Emission Tomography Research Centre, Hull York Medical School and University of Hull, Cottingham Road, Hull, HU6 7RX, UK

2. The University of Manchester, Division of Pharmacy and Optometry, School of Health Sciences, Faculty of Biology, Medicine and Health, Manchester, UK

3. KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute, Laboratory of Virology and Chemotherapy, Leuven, Belgium

4. Department of Chemistry and Physics, Southwestern Oklahoma State University, Weatherford, OK 73096, USA

5. School of Biomedical Engineering and Imaging Sciences, King's College London, 4th Floor Lambeth Wing, St Thomas’ Hospital, London, SE1 7EH, UK

Abstract

Alkylation of secondary amines on side-bridged cyclam derivatives locks the resulting metal complex in the trans-IV configuration. These derivatives offer new perspectives for the design and development of CXCR4-targeted therapeutic agents.

Funder

Yorkshire Cancer Research

KU Leuven

University of Hull

Medical Research Council

Publisher

Royal Society of Chemistry (RSC)

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