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Integrin antagonists

G. P. Curley1, H. Blum2 and M. J. Humphries1

(1)  School of Biological Sciences, University of Manchester, Oxford Road, Manchester M13 9PT (UK), GB
(2)  Hoechst Marion Roussel, DG Rheumatic/Autoimmune Diseases, D-65926 Frankfurt (Germany), e-mail: Martin.Humphries@man.ac.uk, DE
Abstract.   Integrins are a family of cell surface glycoproteins that mediate numerous cell-cell and cell-matrix interactions and are involved in biological processes such as tissue morphogenesis, leukocyte recirculation and migration, wound healing, blood clotting and immune response. Aberrant cell adhesion has been implicated in the pathogenesis of several diseases, including a number of inflammatory disorders such as rheumatoid arthritis, inflammatory bowel disease and asthma, as well as cancer and coronary heart disease. As such integrins are seen as excellent targets for the development of therapeutic agents. This report begins with an examination of the structure of integrin molecules and their ligands and then goes on to review the current state of development of antiintegrin antagonists.

Key words. Integrins; cell adhesion; antagonists; inflammation; cancer; arthritis; therapeutics.

Received 13 April 1999; received after revision 28 May 1999; accepted 28 May 1999



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  1. Cardillo, Giuliana (2009) Dehydro- -amino Acid Containing Peptides as Promising Sequences for Drug Development. European Journal of Organic Chemistry 2009(34)
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  3. Gentilucci, Luca (2009) Synthesis and Conformational Analysis of Cyclotetrapeptide Mimetic β-Turn Templates and Validation as 3D Scaffolds. ChemMedChem
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  4. Heckmann, Dominik (2007) Rationales Design von hoch aktiven und selektiven Liganden für α5β1- und αvβ3-Integrine. Angewandte Chemie
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  5. Heckmann, Dominik (2007) Probing Integrin Selectivity: Rational Design of Highly Active and Selective Ligands for the α5β1 and αvβ3 Integrin Receptor. Angewandte Chemie International Edition
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