Configurationally Restricted Bismacrocyclic CXCR4 Receptor Antagonists-Reference-Cited by-同舟云学术

Configurationally Restricted Bismacrocyclic CXCR4 Receptor Antagonists

Published:2006-09-02 Issue:21 Volume:49 Page:6162-6165
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Valks Gina C.¹,McRobbie Graeme¹,Lewis Elizabeth A.¹,Hubin Timothy J.¹,Hunter Tina M.¹,Sadler Peter J.¹,Pannecouque Christophe¹,De Clercq Erik¹,Archibald Stephen J.¹

Affiliation:

1. Department of Chemistry and Clinical Biosciences Institute, University of Hull, Hull, HU6 7RX, United Kingdom, Department of Chemistry and Physics, Southwestern Oklahoma State University, 100 Campus Drive, Weatherford, Oklahoma 73096, School of Chemistry, The University of Edinburgh, West Mains Road, Edinburgh, EH9 3JJ, United Kingdom, and Rega Institute for Medical Research, Katholieke Universiteit Leuven B-3000 Leuven, Belgium

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm0607810

Reference24 articles.

1. Metal Ion Enhanced Binding of AMD3100 to Asp262 in the CXCR4 Receptor

2. Configurations of metallocyclams and relevance to anti-HIV activity

3. Chemokines, chemokine receptors and small-molecule antagonists: recent developments

4. Synthesis and Structure-Activity Relationships of Phenylenebis(methylene)-Linked Bis-Tetraazamacrocycles That Inhibit HIV Replication. Effects of Macrocyclic Ring Size and Substituents on the Aromatic Linker

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