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Author Spotlight: Development of a Method for Identifying Small Molecular Antagonists of β2 Integrin Activation
Published on: February 2, 2024
Design, Synthesis, and Biological Evaluation of α4 β1 Integrin Antagonists Based on β-D-Mannose as Rigid Scaffold
Jürgen Boer1, Dirk Gottschling1, Anja Schuster2
1Institut für Organische Chemie und Biochemie Technische Universität München Lichtenbergstrasse 4, 85747 Garching (Germany) Fax: (+49) 89-289-13210.
Abstract:
A cyclic peptide role model was used for the design and synthesis of a new class of biologically active and α4 -selective integrin antagonists (e.g. 1) based on β-D-mannose. These carbohydrate-based peptidomimetics were synthesized to include the functional groups of their cyclic peptide precursors without the redundant amide backbone.
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